Commit
•
a5b3296
1
Parent(s):
142ebc9
Upload name_reaction.csv
Browse files- name_reaction.csv +829 -0
name_reaction.csv
ADDED
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1 |
+
name,link
|
2 |
+
appel-reaction,https://www.name-reaction.com/appel-reaction
|
3 |
+
baeyer-villiger-oxidation,https://www.name-reaction.com/baeyer-villiger-oxidation
|
4 |
+
bartoli-indole-synthesis,https://www.name-reaction.com/bartoli-indole-synthesis
|
5 |
+
baylis-hillman-reaction,https://www.name-reaction.com/baylis-hillman-reaction
|
6 |
+
beckmann-rearrangement,https://www.name-reaction.com/beckmann-rearrangement
|
7 |
+
biginelli-reaction,https://www.name-reaction.com/biginelli-reaction
|
8 |
+
birch-reduction,https://www.name-reaction.com/birch-reduction
|
9 |
+
buchwald-hartwig-amination,https://www.name-reaction.com/buchwald-hartwig-amination
|
10 |
+
cannizzaro-reaction,https://www.name-reaction.com/cannizzaro-reaction
|
11 |
+
claisen-condensation,https://www.name-reaction.com/claisen-condensation
|
12 |
+
claisen-rearrangement,https://www.name-reaction.com/claisen-rearrangement
|
13 |
+
clemmensen-reduction,https://www.name-reaction.com/clemmensen-reduction
|
14 |
+
cope-rearrangement,https://www.name-reaction.com/cope-rearrangement
|
15 |
+
corey-kim-oxidation,https://www.name-reaction.com/corey-kim-oxidation
|
16 |
+
curtius-rearrangement,https://www.name-reaction.com/curtius-rearrangement
|
17 |
+
dakin-west-reaction,https://www.name-reaction.com/dakin-west-reaction
|
18 |
+
dieckmann-condensation,https://www.name-reaction.com/dieckmann-condensation
|
19 |
+
diels-alder-reaction,https://www.name-reaction.com/diels-alder-reaction
|
20 |
+
eschenmoser-claisen-rearrangement,https://www.name-reaction.com/eschenmoser-claisen-rearrangement
|
21 |
+
eschweiler-clarke-reaction,https://www.name-reaction.com/eschweiler-clarke-reaction
|
22 |
+
finkelstein-reaction,https://www.name-reaction.com/finkelstein-reaction
|
23 |
+
fischer-esterification,https://www.name-reaction.com/fischer-esterification
|
24 |
+
fischer-indole-synthesis,https://www.name-reaction.com/fischer-indole-synthesis
|
25 |
+
friedel-crafts-acylation,https://www.name-reaction.com/friedel-crafts-acylation
|
26 |
+
friedel-crafts-alkylation,https://www.name-reaction.com/friedel-crafts-alkylation
|
27 |
+
fries-rearrangement,https://www.name-reaction.com/fries-rearrangement
|
28 |
+
gabriel-synthesis,https://www.name-reaction.com/gabriel-synthesis
|
29 |
+
grignard-reaction,https://www.name-reaction.com/grignard-reaction
|
30 |
+
heck-reaction,https://www.name-reaction.com/heck-reaction
|
31 |
+
hell-volhard-zelinsky-reaction,https://www.name-reaction.com/hell-volhard-zelinsky-reaction
|
32 |
+
henry-reaction,https://www.name-reaction.com/henry-reaction
|
33 |
+
hofmann-elimination,https://www.name-reaction.com/hofmann-elimination
|
34 |
+
hofmann-rearrangement,https://www.name-reaction.com/hofmann-rearrangement
|
35 |
+
ireland-claisen-rearrangement,https://www.name-reaction.com/ireland-claisen-rearrangement
|
36 |
+
johnson-claisen-rearrangement,https://www.name-reaction.com/johnson-claisen-rearrangement
|
37 |
+
jones-oxidation,https://www.name-reaction.com/jones-oxidation
|
38 |
+
knoevenagel-condensation,https://www.name-reaction.com/knoevenagel-condensation
|
39 |
+
knorr-pyrazole-synthesis,https://www.name-reaction.com/knorr-pyrazole-synthesis
|
40 |
+
kolbe-schmitt-reaction,https://www.name-reaction.com/kolbe-schmitt-reaction
|
41 |
+
kumada-cross-coupling,https://www.name-reaction.com/kumada-cross-coupling
|
42 |
+
luche-reduction,https://www.name-reaction.com/luche-reduction
|
43 |
+
mannich-reaction,https://www.name-reaction.com/mannich-reaction
|
44 |
+
michael-addition,https://www.name-reaction.com/michael-addition
|
45 |
+
mitsunobu-reaction,https://www.name-reaction.com/mitsunobu-reaction
|
46 |
+
mukaiyama-aldol-addition,https://www.name-reaction.com/mukaiyama-aldol-addition
|
47 |
+
n,https://www.name-reaction.com/n
|
48 |
+
negishi-cross-coupling,https://www.name-reaction.com/negishi-cross-coupling
|
49 |
+
oppenauer-oxidation,https://www.name-reaction.com/oppenauer-oxidation
|
50 |
+
pauson-khand-reaction,https://www.name-reaction.com/pauson-khand-reaction
|
51 |
+
perkin-reaction,https://www.name-reaction.com/perkin-reaction
|
52 |
+
pictet-spengler-reaction,https://www.name-reaction.com/pictet-spengler-reaction
|
53 |
+
prins-reaction,https://www.name-reaction.com/prins-reaction
|
54 |
+
reformatsky-reaction,https://www.name-reaction.com/reformatsky-reaction
|
55 |
+
reimer-tiemann-reaction,https://www.name-reaction.com/reimer-tiemann-reaction
|
56 |
+
ritter-reaction,https://www.name-reaction.com/ritter-reaction
|
57 |
+
robinson-annulation,https://www.name-reaction.com/robinson-annulation
|
58 |
+
sandmeyer-reaction,https://www.name-reaction.com/sandmeyer-reaction
|
59 |
+
schmidt-reaction,https://www.name-reaction.com/schmidt-reaction
|
60 |
+
schotten-baumann-reaction,https://www.name-reaction.com/schotten-baumann-reaction
|
61 |
+
sharpless-epoxidation,https://www.name-reaction.com/sharpless-epoxidation
|
62 |
+
sonogashira-cross-coupling,https://www.name-reaction.com/sonogashira-cross-coupling
|
63 |
+
staudinger-reaction,https://www.name-reaction.com/staudinger-reaction
|
64 |
+
stille-cross-coupling,https://www.name-reaction.com/stille-cross-coupling
|
65 |
+
strecker-amino-acid-synthesis,https://www.name-reaction.com/strecker-amino-acid-synthesis
|
66 |
+
suzuki-cross-coupling,https://www.name-reaction.com/suzuki-cross-coupling
|
67 |
+
swern-oxidation,https://www.name-reaction.com/swern-oxidation
|
68 |
+
ullmann-reaction,https://www.name-reaction.com/ullmann-reaction
|
69 |
+
vilsmeier-haack-reaction,https://www.name-reaction.com/vilsmeier-haack-reaction
|
70 |
+
wagner-meerwein-rearrangement,https://www.name-reaction.com/wagner-meerwein-rearrangement
|
71 |
+
williamson-ether-synthesis,https://www.name-reaction.com/williamson-ether-synthesis
|
72 |
+
wittig-reaction,https://www.name-reaction.com/wittig-reaction
|
73 |
+
wolff-rearrangement,https://www.name-reaction.com/wolff-rearrangement
|
74 |
+
wolff-kishner-reduction,https://www.name-reaction.com/wolff-kishner-reduction
|
75 |
+
wurtz-reaction,https://www.name-reaction.com/wurtz-reaction
|
76 |
+
yamaguchi-esterification,https://www.name-reaction.com/yamaguchi-esterification
|
77 |
+
0-9[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=1
|
78 |
+
"1,2-Wittig rearrangement","https://en.wikipedia.org/wiki/1,2-Wittig_rearrangement"
|
79 |
+
"1,3-Dipolar cycloaddition","https://en.wikipedia.org/wiki/1,3-Dipolar_cycloaddition"
|
80 |
+
"2,3-Wittig rearrangement","https://en.wikipedia.org/wiki/2,3-Wittig_rearrangement"
|
81 |
+
A[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=2
|
82 |
+
Abramovitch�Shapiro tryptamine synthesis,https://en.wikipedia.org/wiki/Tryptamine
|
83 |
+
Acetalisation,https://en.wikipedia.org/wiki/Acetalisation
|
84 |
+
Acetoacetic ester condensation,https://en.wikipedia.org/wiki/Acetoacetic_ester_condensation
|
85 |
+
Achmatowicz reaction,https://en.wikipedia.org/wiki/Achmatowicz_reaction
|
86 |
+
Acylation,https://en.wikipedia.org/wiki/Acylation
|
87 |
+
Acyloin condensation,https://en.wikipedia.org/wiki/Acyloin_condensation
|
88 |
+
Adams' catalyst,https://en.wikipedia.org/wiki/Adams%27_catalyst
|
89 |
+
Adams decarboxylation,https://en.wikipedia.org/wiki/Adams_decarboxylation
|
90 |
+
Adkins catalyst,https://en.wikipedia.org/wiki/Adkins_catalyst
|
91 |
+
Adkins�Peterson reaction,https://en.wikipedia.org/wiki/Adkins%E2%80%93Peterson_reaction
|
92 |
+
Akabori amino acid reaction,https://en.wikipedia.org/wiki/Akabori_amino_acid_reaction
|
93 |
+
Alcohol oxidation,https://en.wikipedia.org/wiki/Alcohol_oxidation
|
94 |
+
Alder�Stein rules,https://en.wikipedia.org/wiki/Alder%E2%80%93Stein_rules
|
95 |
+
Aldol addition,https://en.wikipedia.org/wiki/Aldol_addition
|
96 |
+
Aldol condensation,https://en.wikipedia.org/wiki/Aldol_condensation
|
97 |
+
Algar�Flynn�Oyamada reaction,https://en.wikipedia.org/wiki/Algar%E2%80%93Flynn%E2%80%93Oyamada_reaction
|
98 |
+
Alkylimino-de-oxo-bisubstitution,https://en.wikipedia.org/wiki/Alkylimino-de-oxo-bisubstitution
|
99 |
+
Alkyne trimerisation,https://en.wikipedia.org/wiki/Alkyne_trimerisation
|
100 |
+
Alkyne zipper reaction,https://en.wikipedia.org/wiki/Alkyne_zipper_reaction
|
101 |
+
Allan�Robinson reaction,https://en.wikipedia.org/wiki/Allan%E2%80%93Robinson_reaction
|
102 |
+
Allylic rearrangement,https://en.wikipedia.org/wiki/Allylic_rearrangement
|
103 |
+
Amadori rearrangement,https://en.wikipedia.org/wiki/Amadori_rearrangement
|
104 |
+
Amine alkylation,https://en.wikipedia.org/wiki/Amine_alkylation
|
105 |
+
Angeli�Rimini reaction,https://en.wikipedia.org/wiki/Angeli%E2%80%93Rimini_reaction
|
106 |
+
Andrussov oxidation,https://en.wikipedia.org/wiki/Andrussov_oxidation
|
107 |
+
Appel reaction,https://en.wikipedia.org/wiki/Appel_reaction
|
108 |
+
Aromatic nitration,https://en.wikipedia.org/wiki/Nitration
|
109 |
+
Arndt�Eistert synthesis,https://en.wikipedia.org/wiki/Arndt%E2%80%93Eistert_synthesis
|
110 |
+
Auwers synthesis,https://en.wikipedia.org/wiki/Auwers_synthesis
|
111 |
+
Azo coupling,https://en.wikipedia.org/wiki/Azo_coupling
|
112 |
+
B[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=3
|
113 |
+
Baeyer�Drewson indigo synthesis,https://en.wikipedia.org/wiki/Baeyer%E2%80%93Drewson_indigo_synthesis
|
114 |
+
Bakeland process (Bakelite),https://en.wikipedia.org/wiki/Bakeland_process_(Bakelite)
|
115 |
+
Bally�Scholl synthesis,https://en.wikipedia.org/wiki/Bally%E2%80%93Scholl_synthesis
|
116 |
+
Bamberger rearrangement,https://en.wikipedia.org/wiki/Bamberger_rearrangement
|
117 |
+
Bamberger triazine synthesis,https://en.wikipedia.org/wiki/Bamberger_triazine_synthesis
|
118 |
+
Bamford�Stevens reaction,https://en.wikipedia.org/wiki/Bamford%E2%80%93Stevens_reaction
|
119 |
+
Barbier reaction,https://en.wikipedia.org/wiki/Barbier_reaction
|
120 |
+
Barbier�Wieland degradation,https://en.wikipedia.org/wiki/Carboxylic_acid
|
121 |
+
Bardhan�Sengupta phenanthrene synthesis,https://en.wikipedia.org/wiki/Bardhan%E2%80%93Senguph_phenanthrene_synthesis
|
122 |
+
Barfoed's test,https://en.wikipedia.org/wiki/Barfoed%27s_test
|
123 |
+
Bargellini reaction,https://en.wikipedia.org/wiki/Bargellini_reaction
|
124 |
+
Barton decarboxylation,https://en.wikipedia.org/wiki/Barton_decarboxylation
|
125 |
+
Barton�Kellogg reaction,https://en.wikipedia.org/wiki/Barton%E2%80%93Kellogg_reaction
|
126 |
+
Barton-Zard Synthesis,https://en.wikipedia.org/wiki/Barton-Zard_Synthesis
|
127 |
+
Barton vinyl iodine procedure,https://en.wikipedia.org/wiki/Hydrazone_iodination
|
128 |
+
Baudisch reaction,https://en.wikipedia.org/wiki/Baudisch_reaction
|
129 |
+
Bayer test,https://en.wikipedia.org/wiki/Bayer_test
|
130 |
+
Baylis�Hillman reaction,https://en.wikipedia.org/wiki/Baylis%E2%80%93Hillman_reaction
|
131 |
+
Bechamp reaction,https://en.wikipedia.org/wiki/Bechamp_reaction
|
132 |
+
Bechamp reduction,https://en.wikipedia.org/wiki/Bechamp_reduction
|
133 |
+
Beckmann fragmentation,https://en.wikipedia.org/wiki/Beckmann_fragmentation
|
134 |
+
Beckmann rearrangement,https://en.wikipedia.org/wiki/Beckmann_rearrangement
|
135 |
+
Bellus�Claisen rearrangement,https://en.wikipedia.org/wiki/Bellus%E2%80%93Claisen_rearrangement
|
136 |
+
Belousov�Zhabotinsky reaction,https://en.wikipedia.org/wiki/Belousov%E2%80%93Zhabotinsky_reaction
|
137 |
+
Benary reaction,https://en.wikipedia.org/wiki/Benary_reaction
|
138 |
+
Benedict's reagent,https://en.wikipedia.org/wiki/Benedict%27s_reagent
|
139 |
+
Benkeser reaction,https://en.wikipedia.org/wiki/Benkeser_reaction
|
140 |
+
Benzidine rearrangement,https://en.wikipedia.org/wiki/Benzidine_rearrangement
|
141 |
+
Benzilic acid rearrangement,https://en.wikipedia.org/wiki/Benzilic_acid_rearrangement
|
142 |
+
Benzoin condensation,https://en.wikipedia.org/wiki/Benzoin_condensation
|
143 |
+
Bergman cyclization,https://en.wikipedia.org/wiki/Bergman_cyclization
|
144 |
+
Bergmann azlactone peptide synthesis,https://en.wikipedia.org/wiki/Bergmann_azlactone_peptide_synthesis
|
145 |
+
Bergmann degradation,https://en.wikipedia.org/wiki/Bergmann_degradation
|
146 |
+
Bergmann�Zervas carbobenzoxy method,https://en.wikipedia.org/wiki/Bergmann%E2%80%93Zervas_carbobenzoxy_method
|
147 |
+
Bernthsen acridine synthesis,https://en.wikipedia.org/wiki/Bernthsen_acridine_synthesis
|
148 |
+
Bestmann's reagent,https://en.wikipedia.org/wiki/Bestmann%27s_reagent
|
149 |
+
Betti reaction,https://en.wikipedia.org/wiki/Betti_reaction
|
150 |
+
Biginelli pyrimidine synthesis,https://en.wikipedia.org/wiki/Biginelli_pyrimidine_synthesis
|
151 |
+
Biginelli reaction,https://en.wikipedia.org/wiki/Biginelli_reaction
|
152 |
+
Bingel reaction,https://en.wikipedia.org/wiki/Bingel_reaction
|
153 |
+
Birch reduction,https://en.wikipedia.org/wiki/Birch_reduction
|
154 |
+
Bischler�M�hlau indole synthesis,https://en.wikipedia.org/wiki/Bischler%E2%80%93M%C3%B6hlau_indole_synthesis
|
155 |
+
Bischler�Napieralski reaction,https://en.wikipedia.org/wiki/Bischler%E2%80%93Napieralski_reaction
|
156 |
+
Biuret test,https://en.wikipedia.org/wiki/Biuret_test
|
157 |
+
Blaise ketone synthesis,https://en.wikipedia.org/wiki/Blaise_ketone_synthesis
|
158 |
+
Blaise reaction,https://en.wikipedia.org/wiki/Blaise_reaction
|
159 |
+
Blanc reaction,https://en.wikipedia.org/wiki/Blanc_reaction
|
160 |
+
Blanc chloromethylation,https://en.wikipedia.org/wiki/Blanc_chloromethylation
|
161 |
+
Blum�Ittah aziridine synthesis,https://en.wikipedia.org/wiki/Blum%E2%80%93Ittah_aziridine_synthesis
|
162 |
+
Bodroux reaction,https://en.wikipedia.org/wiki/Bodroux_reaction
|
163 |
+
Bodroux�Chichibabin aldehyde synthesis,https://en.wikipedia.org/wiki/Bodroux%E2%80%93Chichibabin_aldehyde_synthesis
|
164 |
+
Bogert�Cook synthesis,https://en.wikipedia.org/wiki/Bogert%E2%80%93Cook_synthesis
|
165 |
+
Bohlmann-Rahtz pyridine synthesis,https://en.wikipedia.org/wiki/Bohlmann-Rahtz_pyridine_synthesis
|
166 |
+
Bohn�Schmidt reaction,https://en.wikipedia.org/wiki/Bohn%E2%80%93Schmidt_reaction
|
167 |
+
Boord olefin synthesis,https://en.wikipedia.org/wiki/Boord_olefin_synthesis
|
168 |
+
Borodin reaction,https://en.wikipedia.org/wiki/Borodin_reaction
|
169 |
+
Borsche�Drechsel cyclization,https://en.wikipedia.org/wiki/Borsche%E2%80%93Drechsel_cyclization
|
170 |
+
Bosch�Meiser urea process,https://en.wikipedia.org/wiki/Bosch%E2%80%93Meiser_urea_process
|
171 |
+
Bosch reaction,https://en.wikipedia.org/wiki/Bosch_reaction
|
172 |
+
Bouveault aldehyde synthesis,https://en.wikipedia.org/wiki/Bouveault_aldehyde_synthesis
|
173 |
+
Bouveault�Blanc reduction,https://en.wikipedia.org/wiki/Bouveault%E2%80%93Blanc_reduction
|
174 |
+
Boyland�Sims oxidation,https://en.wikipedia.org/wiki/Boyland%E2%80%93Sims_oxidation
|
175 |
+
Boyer Reaction,https://en.wikipedia.org/wiki/Boyer_Reaction
|
176 |
+
Bredt's rule,https://en.wikipedia.org/wiki/Bredt%27s_rule
|
177 |
+
Brook rearrangement,https://en.wikipedia.org/wiki/Brook_rearrangement
|
178 |
+
Brown hydroboration,https://en.wikipedia.org/wiki/Brown_hydroboration
|
179 |
+
Bucherer carbazole synthesis,https://en.wikipedia.org/wiki/Bucherer_carbazole_synthesis
|
180 |
+
Bucherer reaction,https://en.wikipedia.org/wiki/Bucherer_reaction
|
181 |
+
Bucherer�Bergs reaction,https://en.wikipedia.org/wiki/Bucherer%E2%80%93Bergs_reaction
|
182 |
+
Buchner ring enlargement,https://en.wikipedia.org/wiki/Buchner_ring_enlargement
|
183 |
+
B�chner�Curtius�Schlotterbeck reaction,https://en.wikipedia.org/wiki/B%C3%BCchner%E2%80%93Curtius%E2%80%93Schlotterbeck_reaction
|
184 |
+
Buchwald�Hartwig amination,https://en.wikipedia.org/wiki/Buchwald%E2%80%93Hartwig_amination
|
185 |
+
Bunnett reaction,https://en.wikipedia.org/wiki/Bunnett_reaction
|
186 |
+
Burgess reagent,https://en.wikipedia.org/wiki/Burgess_reagent
|
187 |
+
C[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=4
|
188 |
+
Cadiot�Chodkiewicz coupling,https://en.wikipedia.org/wiki/Cadiot%E2%80%93Chodkiewicz_coupling
|
189 |
+
Cadogan-Sundberg indole synthesis,https://en.wikipedia.org/wiki/Cadogan-Sundberg_indole_synthesis
|
190 |
+
Camps quinoline synthesis,https://en.wikipedia.org/wiki/Camps_quinoline_synthesis
|
191 |
+
Cannizzaro reaction,https://en.wikipedia.org/wiki/Cannizzaro_reaction
|
192 |
+
Carbohydrate acetalisation,https://en.wikipedia.org/wiki/Carbohydrate_acetalisation
|
193 |
+
Carbonyl reduction,https://en.wikipedia.org/wiki/Carbonyl_reduction
|
194 |
+
Carbonylation,https://en.wikipedia.org/wiki/Carbonylation
|
195 |
+
Carbylamine reaction,https://en.wikipedia.org/wiki/Carbylamine_reaction
|
196 |
+
Carroll reaction,https://en.wikipedia.org/wiki/Carroll_reaction
|
197 |
+
Castro�Stephens coupling,https://en.wikipedia.org/wiki/Castro%E2%80%93Stephens_coupling
|
198 |
+
Catalytic reforming,https://en.wikipedia.org/wiki/Catalytic_reforming
|
199 |
+
Catellani Reaction,https://en.wikipedia.org/wiki/Catellani_Reaction
|
200 |
+
CBS reduction,https://en.wikipedia.org/wiki/CBS_reduction
|
201 |
+
Chan�Lam coupling,https://en.wikipedia.org/wiki/Boronic_acid
|
202 |
+
Chapman rearrangement,https://en.wikipedia.org/wiki/Chapman_rearrangement
|
203 |
+
Cheletropic reaction,https://en.wikipedia.org/wiki/Cheletropic_reaction
|
204 |
+
Chichibabin pyridine synthesis,https://en.wikipedia.org/wiki/Chichibabin_pyridine_synthesis
|
205 |
+
Chichibabin reaction,https://en.wikipedia.org/wiki/Chichibabin_reaction
|
206 |
+
Chiral pool synthesis,https://en.wikipedia.org/wiki/Chiral_pool_synthesis
|
207 |
+
Chugaev elimination,https://en.wikipedia.org/wiki/Chugaev_elimination
|
208 |
+
Ciamician�Dennstedt rearrangement,https://en.wikipedia.org/wiki/Ciamician%E2%80%93Dennstedt_rearrangement
|
209 |
+
Claisen condensation,https://en.wikipedia.org/wiki/Claisen_condensation
|
210 |
+
Claisen rearrangement,https://en.wikipedia.org/wiki/Claisen_rearrangement
|
211 |
+
Claisen�Schmidt condensation,https://en.wikipedia.org/wiki/Claisen%E2%80%93Schmidt_condensation
|
212 |
+
Clemmensen reduction,https://en.wikipedia.org/wiki/Clemmensen_reduction
|
213 |
+
Collins reagent,https://en.wikipedia.org/wiki/Collins_reagent
|
214 |
+
Combes quinoline synthesis,https://en.wikipedia.org/wiki/Combes_quinoline_synthesis
|
215 |
+
Conia reaction,https://en.wikipedia.org/wiki/Conia_reaction
|
216 |
+
Conrad�Limpach synthesis,https://en.wikipedia.org/wiki/Conrad%E2%80%93Limpach_synthesis
|
217 |
+
Cook�Heilbron thiazole synthesis,https://en.wikipedia.org/wiki/Cook%E2%80%93Heilbron_thiazole_synthesis
|
218 |
+
Cope elimination,https://en.wikipedia.org/wiki/Cope_elimination
|
219 |
+
Corey reagent,https://en.wikipedia.org/wiki/Corey_reagent
|
220 |
+
Corey�Bakshi�Shibata reduction,https://en.wikipedia.org/wiki/Corey%E2%80%93Bakshi%E2%80%93Shibata_reduction
|
221 |
+
Corey�Fuchs reaction,https://en.wikipedia.org/wiki/Corey%E2%80%93Fuchs_reaction
|
222 |
+
Corey�Gilman�Ganem oxidation,https://en.wikipedia.org/wiki/Corey%E2%80%93Gilman%E2%80%93Ganem_oxidation
|
223 |
+
Corey�Kim oxidation,https://en.wikipedia.org/wiki/Corey%E2%80%93Kim_oxidation
|
224 |
+
Corey-Nicolaou macrolactonization,https://en.wikipedia.org/wiki/Corey-Nicolaou_macrolactonization
|
225 |
+
"Corey�Posner, Whitesides�House reaction","https://en.wikipedia.org/wiki/Corey%E2%80%93Posner,_Whitesides%E2%80%93House_reaction"
|
226 |
+
Corey-Seebach reaction,https://en.wikipedia.org/wiki/Corey-Seebach_reaction
|
227 |
+
Corey�Winter olefin synthesis,https://en.wikipedia.org/wiki/Corey%E2%80%93Winter_olefin_synthesis
|
228 |
+
Corey�Winter reaction,https://en.wikipedia.org/wiki/Corey%E2%80%93Winter_reaction
|
229 |
+
Cornforth rearrangement,https://en.wikipedia.org/wiki/Cornforth_rearrangement
|
230 |
+
Coupling reaction,https://en.wikipedia.org/wiki/Coupling_reaction
|
231 |
+
Crabb� reaction,https://en.wikipedia.org/wiki/Crabb%C3%A9_reaction
|
232 |
+
Craig method,https://en.wikipedia.org/wiki/Craig_method
|
233 |
+
Cram's rule of asymmetric induction,https://en.wikipedia.org/wiki/Cram%27s_rule_of_asymmetric_induction
|
234 |
+
Creighton process,https://en.wikipedia.org/wiki/Creighton_process
|
235 |
+
Criegee reaction,https://en.wikipedia.org/wiki/Criegee_reaction
|
236 |
+
Criegee rearrangement,https://en.wikipedia.org/wiki/Criegee_rearrangement
|
237 |
+
Cross metathesis,https://en.wikipedia.org/wiki/Cross_metathesis
|
238 |
+
Crum Brown�Gibson rule,https://en.wikipedia.org/wiki/Crum_Brown%E2%80%93Gibson_rule
|
239 |
+
Curtius degradation,https://en.wikipedia.org/wiki/Curtius_degradation
|
240 |
+
Cyanohydrin reaction,https://en.wikipedia.org/wiki/Cyanohydrin_reaction
|
241 |
+
D[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=5
|
242 |
+
Dakin reaction�(aka Dakin oxidation),https://en.wikipedia.org/wiki/Dakin_reaction
|
243 |
+
Dakin�West reaction,https://en.wikipedia.org/wiki/Dakin%E2%80%93West_reaction
|
244 |
+
Danheiser annulation,https://en.wikipedia.org/wiki/Danheiser_annulation
|
245 |
+
Danheiser benzannulation,https://en.wikipedia.org/wiki/Danheiser_benzannulation
|
246 |
+
Darapsky degradation,https://en.wikipedia.org/wiki/Darapsky_degradation
|
247 |
+
Darzens halogenation,https://en.wikipedia.org/wiki/Darzens_halogenation
|
248 |
+
Darzens synthesis of unsaturated ketones,https://en.wikipedia.org/wiki/Darzens_synthesis_of_unsaturated_ketones
|
249 |
+
Darzens tetralin synthesis,https://en.wikipedia.org/wiki/Darzens_tetralin_synthesis
|
250 |
+
Davis�Beirut reaction,https://en.wikipedia.org/wiki/Davis%E2%80%93Beirut_reaction
|
251 |
+
De Kimpe aziridine synthesis,https://en.wikipedia.org/wiki/De_Kimpe_aziridine_synthesis
|
252 |
+
Dehydration reaction,https://en.wikipedia.org/wiki/Dehydration_reaction
|
253 |
+
Dehydrogenation,https://en.wikipedia.org/wiki/Dehydrogenation
|
254 |
+
Del�pine reaction,https://en.wikipedia.org/wiki/Delepine_reaction
|
255 |
+
DeMayo reaction,https://en.wikipedia.org/wiki/DeMayo_reaction
|
256 |
+
Demjanov rearrangement,https://en.wikipedia.org/wiki/Demjanov_rearrangement
|
257 |
+
Demjanow desamination,https://en.wikipedia.org/wiki/Demjanow_desamination
|
258 |
+
Dess�Martin oxidation,https://en.wikipedia.org/wiki/Dess%E2%80%93Martin_oxidation
|
259 |
+
"Diazoalkane 1,3-dipolar cycloaddition","https://en.wikipedia.org/wiki/Diazoalkane_1,3-dipolar_cycloaddition"
|
260 |
+
Diazotisation,https://en.wikipedia.org/wiki/Diazotisation
|
261 |
+
DIBAL-H selective reduction,https://en.wikipedia.org/wiki/DIBAL
|
262 |
+
Dieckmann condensation,https://en.wikipedia.org/wiki/Dieckmann_condensation
|
263 |
+
Dieckmann reaction,https://en.wikipedia.org/wiki/Dieckmann_reaction
|
264 |
+
Diels�Alder reaction,https://en.wikipedia.org/wiki/Diels%E2%80%93Alder_reaction
|
265 |
+
Diels�Reese reaction,https://en.wikipedia.org/wiki/Diels%E2%80%93Reese_reaction
|
266 |
+
Dienol�benzene rearrangement,https://en.wikipedia.org/wiki/Dienol%E2%80%93benzene_rearrangement
|
267 |
+
Dienone�phenol rearrangement,https://en.wikipedia.org/wiki/Dienone%E2%80%93phenol_rearrangement
|
268 |
+
Dimroth rearrangement,https://en.wikipedia.org/wiki/Dimroth_rearrangement
|
269 |
+
Di-?-methane rearrangement,https://en.wikipedia.org/wiki/Di-%CF%80-methane_rearrangement
|
270 |
+
Directed ortho metalation,https://en.wikipedia.org/wiki/Directed_ortho_metalation
|
271 |
+
Doebner modification,https://en.wikipedia.org/wiki/Doebner_modification
|
272 |
+
Doebner reaction,https://en.wikipedia.org/wiki/Doebner_reaction
|
273 |
+
Doering�LaFlamme carbon chain extension,https://en.wikipedia.org/wiki/Doering%E2%80%93LaFlamme_carbon_chain_extension
|
274 |
+
D�tz reaction,https://en.wikipedia.org/wiki/D%C3%B6tz_reaction
|
275 |
+
Dowd�Beckwith ring expansion reaction,https://en.wikipedia.org/wiki/Dowd%E2%80%93Beckwith_ring_expansion_reaction
|
276 |
+
Duff reaction,https://en.wikipedia.org/wiki/Duff_reaction
|
277 |
+
Dutt�Wormall reaction,https://en.wikipedia.org/wiki/Dutt%E2%80%93Wormall_reaction
|
278 |
+
Dyotropic reaction,https://en.wikipedia.org/wiki/Dyotropic_reaction
|
279 |
+
E[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=6
|
280 |
+
E1cB elimination reaction,https://en.wikipedia.org/wiki/E1cB_elimination_reaction
|
281 |
+
Eder reaction,https://en.wikipedia.org/wiki/Eder_reaction
|
282 |
+
Edman degradation,https://en.wikipedia.org/wiki/Edman_degradation
|
283 |
+
Eglinton reaction,https://en.wikipedia.org/wiki/Eglinton_reaction
|
284 |
+
Ehrlich�Sachs reaction,https://en.wikipedia.org/wiki/Ehrlich%E2%80%93Sachs_reaction
|
285 |
+
Einhorn variant,https://en.wikipedia.org/wiki/Einhorn_variant
|
286 |
+
Einhorn�Brunner reaction,https://en.wikipedia.org/wiki/Einhorn%E2%80%93Brunner_reaction
|
287 |
+
Elbs persulfate oxidation,https://en.wikipedia.org/wiki/Elbs_persulfate_oxidation
|
288 |
+
Elbs reaction,https://en.wikipedia.org/wiki/Elbs_reaction
|
289 |
+
Electrochemical fluorination,https://en.wikipedia.org/wiki/Electrochemical_fluorination
|
290 |
+
Electrocyclic reaction,https://en.wikipedia.org/wiki/Electrocyclic_reaction
|
291 |
+
Electrophilic halogenation,https://en.wikipedia.org/wiki/Electrophilic_halogenation
|
292 |
+
Electrophilic amination,https://en.wikipedia.org/wiki/Electrophilic_amination
|
293 |
+
Elimination reaction,https://en.wikipedia.org/wiki/Elimination_reaction
|
294 |
+
Emde degradation,https://en.wikipedia.org/wiki/Emde_degradation
|
295 |
+
Emmert reaction,https://en.wikipedia.org/wiki/Emmert_reaction
|
296 |
+
Enders SAMP/RAMP hydrazone-alkylation reaction,https://en.wikipedia.org/wiki/Enders_SAMP/RAMP_hydrazone-alkylation_reaction
|
297 |
+
Ene reaction,https://en.wikipedia.org/wiki/Ene_reaction
|
298 |
+
Enyne metathesis,https://en.wikipedia.org/wiki/Enyne_metathesis
|
299 |
+
Epoxidation,https://en.wikipedia.org/wiki/Epoxidation
|
300 |
+
Erlenmeyer�Pl�chl azlactone and amino-acid synthesis,https://en.wikipedia.org/wiki/Erlenmeyer%E2%80%93Pl%C3%B6chl_azlactone_and_amino-acid_synthesis
|
301 |
+
Eschenmoser fragmentation,https://en.wikipedia.org/wiki/Eschenmoser_fragmentation
|
302 |
+
Eschenmoser sulfide contraction,https://en.wikipedia.org/wiki/Eschenmoser_sulfide_contraction
|
303 |
+
Eschweiler�Clarke reaction,https://en.wikipedia.org/wiki/Eschweiler%E2%80%93Clarke_reaction
|
304 |
+
Ester pyrolysis,https://en.wikipedia.org/wiki/Ester_pyrolysis
|
305 |
+
Ether cleavage,https://en.wikipedia.org/wiki/Ether
|
306 |
+
�tard reaction,https://en.wikipedia.org/wiki/%C3%89tard_reaction
|
307 |
+
Evans aldol,https://en.wikipedia.org/wiki/Evans_aldol
|
308 |
+
Evans�Saksena reduction,https://en.wikipedia.org/wiki/Evans%E2%80%93Saksena_reduction
|
309 |
+
Evans�Tishchenko reaction,https://en.wikipedia.org/wiki/Evans%E2%80%93Tishchenko_reaction
|
310 |
+
F[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=7
|
311 |
+
Favorskii reaction,https://en.wikipedia.org/wiki/Favorskii_reaction
|
312 |
+
Favorskii rearrangement,https://en.wikipedia.org/wiki/Favorskii_rearrangement
|
313 |
+
Favorskii�Babayan synthesis,https://en.wikipedia.org/wiki/Favorskii%E2%80%93Babayan_synthesis
|
314 |
+
Fehling test,https://en.wikipedia.org/wiki/Fehling%27s_solution
|
315 |
+
Feist�Benary synthesis,https://en.wikipedia.org/wiki/Feist%E2%80%93Benary_synthesis
|
316 |
+
Fenton reaction,https://en.wikipedia.org/wiki/Fenton_reaction
|
317 |
+
Ferrario reaction,https://en.wikipedia.org/wiki/Ferrario_reaction
|
318 |
+
Ferrier carbocyclization,https://en.wikipedia.org/wiki/Ferrier_carbocyclization
|
319 |
+
Ferrier rearrangement,https://en.wikipedia.org/wiki/Ferrier_rearrangement
|
320 |
+
F�tizon oxidation,https://en.wikipedia.org/wiki/F%C3%A9tizon_oxidation
|
321 |
+
Fiesselmann thiophene synthesis,https://en.wikipedia.org/wiki/Fiesselmann_thiophene_synthesis
|
322 |
+
Fischer indole synthesis,https://en.wikipedia.org/wiki/Fischer_indole_synthesis
|
323 |
+
Fischer oxazole synthesis,https://en.wikipedia.org/wiki/Fischer_oxazole_synthesis
|
324 |
+
Fischer peptide synthesis,https://en.wikipedia.org/wiki/Fischer_peptide_synthesis
|
325 |
+
Fischer phenylhydrazine and oxazone reaction,https://en.wikipedia.org/wiki/Fischer_phenylhydrazine_and_oxazone_reaction
|
326 |
+
Fischer glycosidation,https://en.wikipedia.org/wiki/Fischer_glycosidation
|
327 |
+
Fischer�Hepp rearrangement,https://en.wikipedia.org/wiki/Fischer%E2%80%93Hepp_rearrangement
|
328 |
+
Fischer�Speier esterification,https://en.wikipedia.org/wiki/Fischer%E2%80%93Speier_esterification
|
329 |
+
Fischer Tropsch synthesis,https://en.wikipedia.org/wiki/Fischer_Tropsch_synthesis
|
330 |
+
Fleming�Tamao oxidation,https://en.wikipedia.org/wiki/Fleming%E2%80%93Tamao_oxidation
|
331 |
+
Flood reaction,https://en.wikipedia.org/wiki/Flood_reaction
|
332 |
+
Folin�Ciocalteu reagent,https://en.wikipedia.org/wiki/Folin%E2%80%93Ciocalteu_reagent
|
333 |
+
Formox process,https://en.wikipedia.org/wiki/Formox_process
|
334 |
+
Forster reaction,https://en.wikipedia.org/wiki/Forster_reaction
|
335 |
+
Forster�Decker method,https://en.wikipedia.org/wiki/Forster%E2%80%93Decker_method
|
336 |
+
Fowler process,https://en.wikipedia.org/wiki/Fluorocarbon
|
337 |
+
Franchimont reaction,https://en.wikipedia.org/wiki/Franchimont_reaction
|
338 |
+
Frankland synthesis,https://en.wikipedia.org/wiki/Frankland_synthesis
|
339 |
+
Frankland�Duppa reaction,https://en.wikipedia.org/wiki/Frankland%E2%80%93Duppa_reaction
|
340 |
+
Fr�ter�Seebach alkylation,https://en.wikipedia.org/wiki/Fr%C3%A1ter%E2%80%93Seebach_alkylation
|
341 |
+
Free radical halogenation,https://en.wikipedia.org/wiki/Free_radical_halogenation
|
342 |
+
Freund reaction,https://en.wikipedia.org/wiki/Freund_reaction
|
343 |
+
Friedel�Crafts acylation,https://en.wikipedia.org/wiki/Friedel%E2%80%93Crafts_reaction
|
344 |
+
Friedel�Crafts alkylation,https://en.wikipedia.org/wiki/Friedel%E2%80%93Crafts_reaction
|
345 |
+
Friedl�nder synthesis,https://en.wikipedia.org/wiki/Friedl%C3%A4nder_synthesis
|
346 |
+
Fries rearrangement,https://en.wikipedia.org/wiki/Fries_rearrangement
|
347 |
+
Fritsch�Buttenberg�Wiechell rearrangement,https://en.wikipedia.org/wiki/Fritsch%E2%80%93Buttenberg%E2%80%93Wiechell_rearrangement
|
348 |
+
Fujimoto�Belleau reaction,https://en.wikipedia.org/wiki/Fujimoto%E2%80%93Belleau_reaction
|
349 |
+
Fujiwara�Moritani reaction,https://en.wikipedia.org/wiki/Fujiwara%E2%80%93Moritani_reaction
|
350 |
+
Fukuyama coupling,https://en.wikipedia.org/wiki/Fukuyama_coupling
|
351 |
+
Fukuyama indole synthesis,https://en.wikipedia.org/wiki/Fukuyama_indole_synthesis
|
352 |
+
Fukuyama reduction,https://en.wikipedia.org/wiki/Fukuyama_reduction
|
353 |
+
G[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=8
|
354 |
+
Gabriel ethylenimine method,https://en.wikipedia.org/wiki/Gabriel_ethylenimine_method
|
355 |
+
Gabriel synthesis,https://en.wikipedia.org/wiki/Gabriel_synthesis
|
356 |
+
Gallagher�Hollander degradation,https://en.wikipedia.org/wiki/Gallagher%E2%80%93Hollander_degradation
|
357 |
+
Gassman indole synthesis,https://en.wikipedia.org/wiki/Gassman_indole_synthesis
|
358 |
+
Gastaldi synthesis,https://en.wikipedia.org/wiki/Gastaldi_synthesis
|
359 |
+
Gattermann aldehyde synthesis,https://en.wikipedia.org/wiki/Gattermann_aldehyde_synthesis
|
360 |
+
Gattermann Koch reaction,https://en.wikipedia.org/wiki/Gattermann_Koch_reaction
|
361 |
+
Gattermann reaction,https://en.wikipedia.org/wiki/Gattermann_reaction
|
362 |
+
Geminal halide hydrolysis,https://en.wikipedia.org/wiki/Geminal_halide_hydrolysis
|
363 |
+
Gewald reaction,https://en.wikipedia.org/wiki/Gewald_reaction
|
364 |
+
Gibbs phthalic anhydride process,https://en.wikipedia.org/wiki/Gibbs_phthalic_anhydride_process
|
365 |
+
Gilman reagent,https://en.wikipedia.org/wiki/Gilman_reagent
|
366 |
+
Glaser coupling,https://en.wikipedia.org/wiki/Glaser_coupling
|
367 |
+
Glycol cleavage,https://en.wikipedia.org/wiki/Glycol_cleavage
|
368 |
+
Gomberg�Bachmann reaction,https://en.wikipedia.org/wiki/Gomberg%E2%80%93Bachmann_reaction
|
369 |
+
Gomberg�Bachmann�Hey reaction,https://en.wikipedia.org/wiki/Gomberg%E2%80%93Bachmann%E2%80%93Hey_reaction
|
370 |
+
Gomberg radical reaction,https://en.wikipedia.org/wiki/Gomberg_radical_reaction
|
371 |
+
Gould�Jacobs reaction,https://en.wikipedia.org/wiki/Gould%E2%80%93Jacobs_reaction
|
372 |
+
Graebe�Ullmann synthesis,https://en.wikipedia.org/wiki/Graebe%E2%80%93Ullmann_synthesis
|
373 |
+
Grignard degradation,https://en.wikipedia.org/wiki/Grignard_degradation
|
374 |
+
Griesbaum coozonolysis,https://en.wikipedia.org/wiki/Griesbaum_coozonolysis
|
375 |
+
Grignard reaction,https://en.wikipedia.org/wiki/Grignard_reaction
|
376 |
+
Grob fragmentation,https://en.wikipedia.org/wiki/Grob_fragmentation
|
377 |
+
Grundmann aldehyde synthesis,https://en.wikipedia.org/wiki/Grundmann_aldehyde_synthesis
|
378 |
+
Gryszkiewicz�Trochimowski and McCombie method,https://en.wikipedia.org/w/index.php?title=Gryszkiewicz%E2%80%93Trochimowski_and_McCombie_method&action=edit&redlink=1
|
379 |
+
Guareschi�Thorpe condensation,https://en.wikipedia.org/wiki/Guareschi%E2%80%93Thorpe_condensation
|
380 |
+
Guerbet reaction,https://en.wikipedia.org/wiki/Guerbet_reaction
|
381 |
+
Gutknecht pyrazine synthesis,https://en.wikipedia.org/wiki/Gutknecht_pyrazine_synthesis
|
382 |
+
H[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=9
|
383 |
+
Hajos�Parrish�Eder�Sauer�Wiechert reaction,https://en.wikipedia.org/wiki/Hajos%E2%80%93Parrish%E2%80%93Eder%E2%80%93Sauer%E2%80%93Wiechert_reaction
|
384 |
+
Haller�Bauer reaction,https://en.wikipedia.org/wiki/Haller%E2%80%93Bauer_reaction
|
385 |
+
Haloform reaction,https://en.wikipedia.org/wiki/Haloform_reaction
|
386 |
+
Halogen addition reaction,https://en.wikipedia.org/wiki/Halogen_addition_reaction
|
387 |
+
Halohydrin formation reaction,https://en.wikipedia.org/wiki/Halohydrin_formation_reaction
|
388 |
+
Hammett equation,https://en.wikipedia.org/wiki/Hammett_equation
|
389 |
+
Hammick reaction,https://en.wikipedia.org/wiki/Hammick_reaction
|
390 |
+
Hantzsch pyrrole synthesis,https://en.wikipedia.org/wiki/Hantzsch_pyrrole_synthesis
|
391 |
+
Hantzsch�Collidin synthesis,https://en.wikipedia.org/wiki/Hantzsch%E2%80%93Collidin_synthesis
|
392 |
+
Harries ozonide reaction,https://en.wikipedia.org/wiki/Harries_ozonide_reaction
|
393 |
+
Haworth methylation,https://en.wikipedia.org/wiki/Haworth_methylation
|
394 |
+
Haworth Phenanthrene synthesis,https://en.wikipedia.org/wiki/Haworth_Phenanthrene_synthesis
|
395 |
+
Haworth reaction,https://en.wikipedia.org/wiki/Haworth_reaction
|
396 |
+
Hay coupling,https://en.wikipedia.org/wiki/Hay_coupling
|
397 |
+
Hayashi rearrangement,https://en.wikipedia.org/wiki/Hayashi_rearrangement
|
398 |
+
Heck reaction,https://en.wikipedia.org/wiki/Heck_reaction
|
399 |
+
Hegedus indole synthesis,https://en.wikipedia.org/wiki/Hegedus_indole_synthesis
|
400 |
+
Helferich method,https://en.wikipedia.org/wiki/Helferich_method
|
401 |
+
Hell�Volhard�Zelinsky halogenation,https://en.wikipedia.org/wiki/Hell%E2%80%93Volhard%E2%80%93Zelinsky_halogenation
|
402 |
+
Hemetsberger indole synthesis,https://en.wikipedia.org/wiki/Hemetsberger_indole_synthesis
|
403 |
+
Hemetsberger�Knittel synthesis,https://en.wikipedia.org/wiki/Hemetsberger%E2%80%93Knittel_synthesis
|
404 |
+
Herzig�Meyer alkimide group determination,https://en.wikipedia.org/wiki/Herzig%E2%80%93Meyer_alkimide_group_determination
|
405 |
+
Heumann indigo synthesis,https://en.wikipedia.org/wiki/Heumann_indigo_synthesis
|
406 |
+
Hiyama coupling,https://en.wikipedia.org/wiki/Hiyama_coupling
|
407 |
+
Hydration reaction,https://en.wikipedia.org/wiki/Hydration_reaction
|
408 |
+
Hydroamination,https://en.wikipedia.org/wiki/Hydroamination
|
409 |
+
Hydrodesulfurization,https://en.wikipedia.org/wiki/Hydrodesulfurization
|
410 |
+
Hydrogenolysis,https://en.wikipedia.org/wiki/Hydrogenolysis
|
411 |
+
Hydrosilylation,https://en.wikipedia.org/wiki/Hydrosilylation
|
412 |
+
Hinsberg indole synthesis,https://en.wikipedia.org/wiki/Hinsberg_indole_synthesis
|
413 |
+
Hinsberg oxindole synthesis,https://en.wikipedia.org/wiki/Hinsberg_oxindole_synthesis
|
414 |
+
Hinsberg reaction,https://en.wikipedia.org/wiki/Hinsberg_reaction
|
415 |
+
Hinsberg separation,https://en.wikipedia.org/wiki/Hinsberg_separation
|
416 |
+
Hinsberg sulfone synthesis,https://en.wikipedia.org/wiki/Hinsberg_sulfone_synthesis
|
417 |
+
Hirao coupling,https://en.wikipedia.org/wiki/Hirao_coupling
|
418 |
+
Hoch�Campbell ethylenimine synthesis,https://en.wikipedia.org/wiki/Hoch%E2%80%93Campbell_ethylenimine_synthesis
|
419 |
+
Hock rearrangement,https://en.wikipedia.org/wiki/Hock_rearrangement
|
420 |
+
Hofmann bromamide reaction,https://en.wikipedia.org/wiki/Hofmann_rearrangement
|
421 |
+
Hofmann elimination,https://en.wikipedia.org/wiki/Hofmann_elimination
|
422 |
+
Hofmann product,https://en.wikipedia.org/wiki/Hofmann_product
|
423 |
+
Hofmann rearrangement,https://en.wikipedia.org/wiki/Hofmann_rearrangement
|
424 |
+
Hofmann�Martius rearrangement,https://en.wikipedia.org/wiki/Hofmann%E2%80%93Martius_rearrangement
|
425 |
+
Hofmann's rule,https://en.wikipedia.org/wiki/Hofmann%27s_rule
|
426 |
+
Hofmann�Sand reaction,https://en.wikipedia.org/wiki/Hofmann%E2%80%93Sand_reaction
|
427 |
+
Homo rearrangement of steroids,https://en.wikipedia.org/wiki/Homo_rearrangement_of_steroids
|
428 |
+
Hooker reaction,https://en.wikipedia.org/wiki/Hooker_reaction
|
429 |
+
Horner�Wadsworth�Emmons reaction,https://en.wikipedia.org/wiki/Horner%E2%80%93Wadsworth%E2%80%93Emmons_reaction
|
430 |
+
Hoesch reaction,https://en.wikipedia.org/wiki/Hoesch_reaction
|
431 |
+
Hosomi�Sakurai reaction,https://en.wikipedia.org/wiki/Hosomi%E2%80%93Sakurai_reaction
|
432 |
+
Houben�Fischer synthesis,https://en.wikipedia.org/wiki/Houben%E2%80%93Fischer_synthesis
|
433 |
+
Hudlicky fluorination,https://en.wikipedia.org/wiki/Fluorination_with_aminosulfuranes
|
434 |
+
Huisgen cycloaddition,https://en.wikipedia.org/wiki/Huisgen_cycloaddition
|
435 |
+
"Hurd-Mori 1,2,3-thiadiazole synthesis","https://en.wikipedia.org/wiki/Hurd-Mori_1,2,3-thiadiazole_synthesis"
|
436 |
+
Hydroboration,https://en.wikipedia.org/wiki/Hydroboration
|
437 |
+
Hydrocarbon cracking,https://en.wikipedia.org/wiki/Cracking_(chemistry)
|
438 |
+
Hydrohalogenation,https://en.wikipedia.org/wiki/Hydrohalogenation
|
439 |
+
I[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=10
|
440 |
+
Indium mediated allylation,https://en.wikipedia.org/wiki/Indium_mediated_allylation
|
441 |
+
Ing�Manske procedure,https://en.wikipedia.org/wiki/Ing%E2%80%93Manske_procedure
|
442 |
+
Ipso substitution,https://en.wikipedia.org/wiki/Ipso_substitution
|
443 |
+
Ireland�Claisen rearrangement,https://en.wikipedia.org/wiki/Ireland%E2%80%93Claisen_rearrangement
|
444 |
+
Isay reaction,https://en.wikipedia.org/wiki/Isay_reaction
|
445 |
+
Ishikawa reagent,https://en.wikipedia.org/wiki/Ishikawa_reagent
|
446 |
+
trans-cis�isomerism,https://en.wikipedia.org/wiki/Isomer
|
447 |
+
J[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=11
|
448 |
+
Jacobsen epoxidation,https://en.wikipedia.org/wiki/Jacobsen_epoxidation
|
449 |
+
Jacobsen rearrangement,https://en.wikipedia.org/wiki/Jacobsen_rearrangement
|
450 |
+
Janovsky reaction,https://en.wikipedia.org/wiki/Janovsky_reaction
|
451 |
+
Japp�Klingemann reaction,https://en.wikipedia.org/wiki/Japp%E2%80%93Klingemann_reaction
|
452 |
+
Japp�Maitland condensation,https://en.wikipedia.org/wiki/Japp%E2%80%93Maitland_condensation
|
453 |
+
Jocic reaction,https://en.wikipedia.org/wiki/Jocic_reaction
|
454 |
+
Johnson�Claisen rearrangement,https://en.wikipedia.org/wiki/Claisen_rearrangement
|
455 |
+
Jordan�Ullmann�Goldberg synthesis,https://en.wikipedia.org/wiki/Jordan%E2%80%93Ullmann%E2%80%93Goldberg_synthesis
|
456 |
+
K[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=12
|
457 |
+
Kabachnik�Fields reaction,https://en.wikipedia.org/wiki/Kabachnik%E2%80%93Fields_reaction
|
458 |
+
Kharasch�Sosnovsky reaction,https://en.wikipedia.org/wiki/Kharasch%E2%80%93Sosnovsky_reaction
|
459 |
+
Keck asymmetric allylation,https://en.wikipedia.org/wiki/Keck_asymmetric_allylation
|
460 |
+
Ketimine Mannich reaction,https://en.wikipedia.org/wiki/Ketimine_Mannich_reaction
|
461 |
+
Ketone halogenation,https://en.wikipedia.org/wiki/Ketone_halogenation
|
462 |
+
Kiliani�Fischer synthesis,https://en.wikipedia.org/wiki/Kiliani%E2%80%93Fischer_synthesis
|
463 |
+
Kindler reaction,https://en.wikipedia.org/wiki/Kindler_reaction
|
464 |
+
Kishner cyclopropane synthesis,https://en.wikipedia.org/wiki/Kishner_cyclopropane_synthesis
|
465 |
+
Knoevenagel condensation,https://en.wikipedia.org/wiki/Knoevenagel_condensation
|
466 |
+
Knorr pyrazole synthesis,https://en.wikipedia.org/wiki/Knorr_pyrazole_synthesis
|
467 |
+
Knorr pyrrole synthesis,https://en.wikipedia.org/wiki/Knorr_pyrrole_synthesis
|
468 |
+
Knorr quinoline synthesis,https://en.wikipedia.org/wiki/Knorr_quinoline_synthesis
|
469 |
+
Koch�Haaf reaction,https://en.wikipedia.org/wiki/Koch%E2%80%93Haaf_reaction
|
470 |
+
Kochi reaction,https://en.wikipedia.org/wiki/Kochi_reaction
|
471 |
+
Koenigs�Knorr reaction,https://en.wikipedia.org/wiki/Koenigs%E2%80%93Knorr_reaction
|
472 |
+
Kolbe electrolysis,https://en.wikipedia.org/wiki/Kolbe_electrolysis
|
473 |
+
Kolbe nitrile synthesis,https://en.wikipedia.org/wiki/Kolbe_nitrile_synthesis
|
474 |
+
Kolbe�Schmitt reaction,https://en.wikipedia.org/wiki/Kolbe%E2%80%93Schmitt_reaction
|
475 |
+
Kornblum oxidation,https://en.wikipedia.org/wiki/Kornblum_oxidation
|
476 |
+
Kornblum�DeLaMare rearrangement,https://en.wikipedia.org/wiki/Kornblum%E2%80%93DeLaMare_rearrangement
|
477 |
+
Kostanecki acylation,https://en.wikipedia.org/wiki/Kostanecki_acylation
|
478 |
+
Kowalski ester homologation,https://en.wikipedia.org/wiki/Kowalski_ester_homologation
|
479 |
+
Krapcho decarboxylation,https://en.wikipedia.org/wiki/Krapcho_decarboxylation
|
480 |
+
Krische allylation,https://en.wikipedia.org/wiki/Krische_allylation
|
481 |
+
Kr�hnke aldehyde synthesis,https://en.wikipedia.org/wiki/Kr%C3%B6hnke_aldehyde_synthesis
|
482 |
+
Kr�hnke oxidation,https://en.wikipedia.org/wiki/Kr%C3%B6hnke_oxidation
|
483 |
+
Kr�hnke pyridine synthesis,https://en.wikipedia.org/wiki/Kr%C3%B6hnke_pyridine_synthesis
|
484 |
+
Kucherov reaction,https://en.wikipedia.org/wiki/Kucherov_reaction
|
485 |
+
Kuhn�Winterstein reaction,https://en.wikipedia.org/wiki/Kuhn%E2%80%93Winterstein_reaction
|
486 |
+
Kulinkovich reaction,https://en.wikipedia.org/wiki/Kulinkovich_reaction
|
487 |
+
Kumada coupling,https://en.wikipedia.org/wiki/Kumada_coupling
|
488 |
+
L[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=13
|
489 |
+
Larock indole synthesis,https://en.wikipedia.org/wiki/Larock_indole_synthesis
|
490 |
+
Lawesson's reagent,https://en.wikipedia.org/wiki/Lawesson%27s_reagent
|
491 |
+
Lebedev process,https://en.wikipedia.org/wiki/Lebedev_process
|
492 |
+
Lehmstedt�Tanasescu reaction,https://en.wikipedia.org/wiki/Lehmstedt%E2%80%93Tanasescu_reaction
|
493 |
+
Leimgruber�Batcho indole synthesis,https://en.wikipedia.org/wiki/Leimgruber%E2%80%93Batcho_indole_synthesis
|
494 |
+
Letts nitrile synthesis,https://en.wikipedia.org/wiki/Letts_nitrile_synthesis
|
495 |
+
Leuckart reaction,https://en.wikipedia.org/wiki/Leuckart_reaction
|
496 |
+
Leuckart thiophenol reaction,https://en.wikipedia.org/wiki/Leuckart_thiophenol_reaction
|
497 |
+
Leuckart�Wallach reaction,https://en.wikipedia.org/wiki/Leuckart%E2%80%93Wallach_reaction
|
498 |
+
Leuckart amide synthesis,https://en.wikipedia.org/wiki/Amide
|
499 |
+
Levinstein process,https://en.wikipedia.org/wiki/Levinstein_process
|
500 |
+
Ley oxidation,https://en.wikipedia.org/wiki/Ley_oxidation
|
501 |
+
Liebeskind�Srogl coupling,https://en.wikipedia.org/wiki/Liebeskind%E2%80%93Srogl_coupling
|
502 |
+
Liebig melamine synthesis,https://en.wikipedia.org/wiki/Melamine
|
503 |
+
Lindlar catalyst,https://en.wikipedia.org/wiki/Lindlar_catalyst
|
504 |
+
Lobry de Bruyn�Van Ekenstein transformation,https://en.wikipedia.org/wiki/Lobry_de_Bruyn%E2%80%93Van_Ekenstein_transformation
|
505 |
+
Lombardo methylenation,https://en.wikipedia.org/wiki/Lombardo_methylenation
|
506 |
+
Lossen rearrangement,https://en.wikipedia.org/wiki/Lossen_rearrangement
|
507 |
+
Lucas' reagent,https://en.wikipedia.org/wiki/Lucas%27_reagent
|
508 |
+
Luche reduction,https://en.wikipedia.org/wiki/Luche_reduction
|
509 |
+
M[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=14
|
510 |
+
Maillard reaction,https://en.wikipedia.org/wiki/Maillard_reaction
|
511 |
+
Madelung synthesis,https://en.wikipedia.org/wiki/Madelung_synthesis
|
512 |
+
Malonic ester synthesis,https://en.wikipedia.org/wiki/Malonic_ester_synthesis
|
513 |
+
Mannich reaction,https://en.wikipedia.org/wiki/Mannich_reaction
|
514 |
+
Mark�Lam deoxygenation,https://en.wikipedia.org/wiki/Mark%C3%B3%E2%80%93Lam_deoxygenation
|
515 |
+
Marschalk reaction,https://en.wikipedia.org/wiki/Marschalk_reaction
|
516 |
+
Martinet dioxindole synthesis,https://en.wikipedia.org/wiki/Martinet_dioxindole_synthesis
|
517 |
+
McDougall monoprotection,https://en.wikipedia.org/wiki/Silyl_ether
|
518 |
+
McFadyen�Stevens reaction,https://en.wikipedia.org/wiki/McFadyen%E2%80%93Stevens_reaction
|
519 |
+
McMurry reaction,https://en.wikipedia.org/wiki/McMurry_reaction
|
520 |
+
Meerwein arylation,https://en.wikipedia.org/wiki/Meerwein_arylation
|
521 |
+
Meerwein�Ponndorf�Verley reduction,https://en.wikipedia.org/wiki/Meerwein%E2%80%93Ponndorf%E2%80%93Verley_reduction
|
522 |
+
Meisenheimer rearrangement,https://en.wikipedia.org/wiki/Meisenheimer_rearrangement
|
523 |
+
Meissenheimer complex,https://en.wikipedia.org/wiki/Meissenheimer_complex
|
524 |
+
Menshutkin reaction,https://en.wikipedia.org/wiki/Menshutkin_reaction
|
525 |
+
Metal-ion-catalyzed ?-bond rearrangement,https://en.wikipedia.org/wiki/Metal-ion-catalyzed_%CF%83-bond_rearrangement
|
526 |
+
Mesylation,https://en.wikipedia.org/wiki/Mesylate
|
527 |
+
Merckwald asymmetric synthesis,https://en.wikipedia.org/wiki/Merckwald_asymmetric_synthesis
|
528 |
+
Metallo-ene reaction,https://en.wikipedia.org/wiki/Metallo-ene_reaction
|
529 |
+
Methylation,https://en.wikipedia.org/wiki/Methylation
|
530 |
+
Meyer and Hartmann reaction,https://en.wikipedia.org/wiki/Meyer_and_Hartmann_reaction
|
531 |
+
Meyer reaction,https://en.wikipedia.org/wiki/Meyer_reaction
|
532 |
+
Meyer synthesis,https://en.wikipedia.org/wiki/Meyer_synthesis
|
533 |
+
Meyer�Schuster rearrangement,https://en.wikipedia.org/wiki/Meyer%E2%80%93Schuster_rearrangement
|
534 |
+
Michael addition,https://en.wikipedia.org/wiki/Michael_addition
|
535 |
+
Michael condensation,https://en.wikipedia.org/wiki/Michael_condensation
|
536 |
+
Michaelis�Arbuzov reaction,https://en.wikipedia.org/wiki/Michaelis%E2%80%93Arbuzov_reaction
|
537 |
+
Midland Alpine borane reduction,https://en.wikipedia.org/wiki/Midland_Alpine_borane_reduction
|
538 |
+
Mignonac reaction,https://en.wikipedia.org/wiki/Mignonac_reaction
|
539 |
+
Milas hydroxylation�of olefins,https://en.wikipedia.org/wiki/Milas_hydroxylation
|
540 |
+
Minisci reaction,https://en.wikipedia.org/wiki/Minisci_reaction
|
541 |
+
Mislow�Evans rearrangement,https://en.wikipedia.org/wiki/Mislow%E2%80%93Evans_rearrangement
|
542 |
+
Mitsunobu reaction,https://en.wikipedia.org/wiki/Mitsunobu_reaction
|
543 |
+
Miyaura borylation,https://en.wikipedia.org/wiki/Miyaura_borylation
|
544 |
+
Modified Wittig-Claisen tandem reaction,https://en.wikipedia.org/wiki/Modified_Wittig-Claisen_tandem_reaction
|
545 |
+
Molisch's test,https://en.wikipedia.org/wiki/Molisch%27s_test
|
546 |
+
Mozingo reduction,https://en.wikipedia.org/wiki/Mozingo_reduction
|
547 |
+
Mukaiyama hydration,https://en.wikipedia.org/wiki/Mukaiyama_hydration
|
548 |
+
Myers' asymmetric alkylation,https://en.wikipedia.org/wiki/Myers%27_asymmetric_alkylation
|
549 |
+
N[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=15
|
550 |
+
Nametkin rearrangement,https://en.wikipedia.org/wiki/Nametkin_rearrangement
|
551 |
+
Narasaka�Prasad reduction,https://en.wikipedia.org/wiki/Narasaka%E2%80%93Prasad_reduction
|
552 |
+
Nazarov cyclization reaction,https://en.wikipedia.org/wiki/Nazarov_cyclization_reaction
|
553 |
+
Neber rearrangement,https://en.wikipedia.org/wiki/Neber_rearrangement
|
554 |
+
Nef reaction,https://en.wikipedia.org/wiki/Nef_reaction
|
555 |
+
Negishi coupling,https://en.wikipedia.org/wiki/Negishi_coupling
|
556 |
+
Negishi zipper reaction,https://en.wikipedia.org/wiki/Negishi_zipper_reaction
|
557 |
+
Nenitzescu indole synthesis,https://en.wikipedia.org/wiki/Nenitzescu_indole_synthesis
|
558 |
+
Nenitzescu reductive acylation,https://en.wikipedia.org/wiki/Nenitzescu_reductive_acylation
|
559 |
+
Newman�Kwart rearrangement,https://en.wikipedia.org/wiki/Newman%E2%80%93Kwart_rearrangement
|
560 |
+
Nicholas reaction,https://en.wikipedia.org/wiki/Nicholas_reaction
|
561 |
+
Niementowski quinazoline synthesis,https://en.wikipedia.org/wiki/Niementowski_quinazoline_synthesis
|
562 |
+
Niementowski quinoline synthesis,https://en.wikipedia.org/wiki/Niementowski_quinoline_synthesis
|
563 |
+
Nierenstein reaction,https://en.wikipedia.org/wiki/Nierenstein_reaction
|
564 |
+
NIH shift,https://en.wikipedia.org/wiki/NIH_shift
|
565 |
+
Ninhydrin test,https://en.wikipedia.org/wiki/Ninhydrin
|
566 |
+
Nitroaldol reaction,https://en.wikipedia.org/wiki/Nitroaldol_reaction
|
567 |
+
Nitrone-olefin 3+2 cycloaddition,https://en.wikipedia.org/wiki/Nitrone-olefin_3%2B2_cycloaddition
|
568 |
+
Normant reagents,https://en.wikipedia.org/wiki/Normant_reagents
|
569 |
+
Noyori asymmetric hydrogenation,https://en.wikipedia.org/wiki/Noyori_asymmetric_hydrogenation
|
570 |
+
Nozaki�Hiyama�Kishi reaction,https://en.wikipedia.org/wiki/Nozaki%E2%80%93Hiyama%E2%80%93Kishi_reaction
|
571 |
+
Nucleophilic acyl substitution,https://en.wikipedia.org/wiki/Nucleophilic_acyl_substitution
|
572 |
+
O[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=16
|
573 |
+
Ohira�Bestmann reaction,https://en.wikipedia.org/wiki/Ohira%E2%80%93Bestmann_reaction
|
574 |
+
Olah reagent,https://en.wikipedia.org/wiki/Olah_reagent
|
575 |
+
Olefin metathesis,https://en.wikipedia.org/wiki/Olefin_metathesis
|
576 |
+
Oppenauer oxidation,https://en.wikipedia.org/wiki/Oppenauer_oxidation
|
577 |
+
Overman rearrangement,https://en.wikipedia.org/wiki/Overman_rearrangement
|
578 |
+
Oxidative decarboxylation,https://en.wikipedia.org/wiki/Pyruvate_decarboxylation
|
579 |
+
Oxo synthesis,https://en.wikipedia.org/wiki/Oxo_synthesis
|
580 |
+
Oxy-Cope rearrangement,https://en.wikipedia.org/wiki/Oxy-Cope_rearrangement
|
581 |
+
Oxymercuration,https://en.wikipedia.org/wiki/Oxymercuration
|
582 |
+
Oxidation of alcohols to carbonyl compounds,https://en.wikipedia.org/wiki/Oxidation_of_alcohols_to_carbonyl_compounds
|
583 |
+
Ozonolysis,https://en.wikipedia.org/wiki/Ozonolysis
|
584 |
+
P[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=17
|
585 |
+
Paal�Knorr pyrrole synthesis,https://en.wikipedia.org/wiki/Paal%E2%80%93Knorr_pyrrole_synthesis
|
586 |
+
Paal�Knorr synthesis,https://en.wikipedia.org/wiki/Paal%E2%80%93Knorr_synthesis
|
587 |
+
Paneth technique,https://en.wikipedia.org/wiki/Paneth_technique
|
588 |
+
Passerini reaction,https://en.wikipedia.org/wiki/Passerini_reaction
|
589 |
+
Patern�B�chi reaction,https://en.wikipedia.org/wiki/Patern%C3%B2%E2%80%93B%C3%BCchi_reaction
|
590 |
+
Pauson�Khand reaction,https://en.wikipedia.org/wiki/Pauson%E2%80%93Khand_reaction
|
591 |
+
Payne rearrangement,https://en.wikipedia.org/wiki/Payne_rearrangement
|
592 |
+
Pechmann condensation,https://en.wikipedia.org/wiki/Pechmann_condensation
|
593 |
+
Pechmann pyrazole synthesis,https://en.wikipedia.org/wiki/Pechmann_pyrazole_synthesis
|
594 |
+
Pellizzari reaction,https://en.wikipedia.org/wiki/Pellizzari_reaction
|
595 |
+
Pelouze synthesis,https://en.wikipedia.org/wiki/Pelouze_synthesis
|
596 |
+
Peptide synthesis,https://en.wikipedia.org/wiki/Peptide_synthesis
|
597 |
+
Perkin alicyclic synthesis,https://en.wikipedia.org/wiki/Perkin_alicyclic_synthesis
|
598 |
+
Perkin reaction,https://en.wikipedia.org/wiki/Perkin_reaction
|
599 |
+
Perkin rearrangement,https://en.wikipedia.org/wiki/Perkin_rearrangement
|
600 |
+
Perkow reaction,https://en.wikipedia.org/wiki/Perkow_reaction
|
601 |
+
Petasis reaction,https://en.wikipedia.org/wiki/Petasis_reaction
|
602 |
+
Petasis reagent,https://en.wikipedia.org/wiki/Petasis_reagent
|
603 |
+
Peterson olefination,https://en.wikipedia.org/wiki/Peterson_olefination
|
604 |
+
Peterson reaction,https://en.wikipedia.org/wiki/Peterson_reaction
|
605 |
+
Petrenko-Kritschenko piperidone synthesis,https://en.wikipedia.org/wiki/Petrenko-Kritschenko_piperidone_synthesis
|
606 |
+
Pfau�Plattner azulene synthesis,https://en.wikipedia.org/wiki/Pfau%E2%80%93Plattner_azulene_synthesis
|
607 |
+
Pfitzinger reaction,https://en.wikipedia.org/wiki/Pfitzinger_reaction
|
608 |
+
Pfitzner�Moffatt oxidation,https://en.wikipedia.org/wiki/Pfitzner%E2%80%93Moffatt_oxidation
|
609 |
+
Phosphonium coupling,https://en.wikipedia.org/wiki/Phosphonium_coupling
|
610 |
+
Photosynthesis,https://en.wikipedia.org/wiki/Photosynthesis
|
611 |
+
Piancatelli rearrangement,https://en.wikipedia.org/wiki/Piancatelli_rearrangement
|
612 |
+
Pictet�Gams isoquinoline synthesis,https://en.wikipedia.org/wiki/Pictet%E2%80%93Gams_isoquinoline_synthesis
|
613 |
+
Pictet�Hubert reaction,https://en.wikipedia.org/wiki/Pictet%E2%80%93Hubert_reaction
|
614 |
+
Pictet�Spengler tetrahydroisoquinoline synthesis,https://en.wikipedia.org/wiki/Pictet%E2%80%93Spengler_tetrahydroisoquinoline_synthesis
|
615 |
+
Pictet�Spengler reaction,https://en.wikipedia.org/wiki/Pictet%E2%80%93Spengler_reaction
|
616 |
+
Piloty�Robinson pyrrole synthesis,https://en.wikipedia.org/wiki/Piloty%E2%80%93Robinson_pyrrole_synthesis
|
617 |
+
Pinacol coupling reaction,https://en.wikipedia.org/wiki/Pinacol_coupling_reaction
|
618 |
+
Pinacol rearrangement,https://en.wikipedia.org/wiki/Pinacol_rearrangement
|
619 |
+
Pinner amidine synthesis,https://en.wikipedia.org/wiki/Pinner_amidine_synthesis
|
620 |
+
Pinner method for ortho esters,https://en.wikipedia.org/wiki/Pinner_method_for_ortho_esters
|
621 |
+
Pinner reaction,https://en.wikipedia.org/wiki/Pinner_reaction
|
622 |
+
Pinner triazine synthesis,https://en.wikipedia.org/wiki/Pinner_triazine_synthesis
|
623 |
+
Pinnick oxidation,https://en.wikipedia.org/wiki/Pinnick_oxidation
|
624 |
+
Piria reaction,https://en.wikipedia.org/wiki/Piria_reaction
|
625 |
+
Polonovski reaction,https://en.wikipedia.org/wiki/Polonovski_reaction
|
626 |
+
Pomeranz�Fritsch reaction,https://en.wikipedia.org/wiki/Pomeranz%E2%80%93Fritsch_reaction
|
627 |
+
Ponzio reaction,https://en.wikipedia.org/wiki/Ponzio_reaction
|
628 |
+
Prato reaction,https://en.wikipedia.org/wiki/Prato_reaction
|
629 |
+
Prelog strain,https://en.wikipedia.org/wiki/Prelog_strain
|
630 |
+
Prevost reaction,https://en.wikipedia.org/wiki/Prevost_reaction
|
631 |
+
Prileschajew reaction,https://en.wikipedia.org/wiki/Prileschajew_reaction
|
632 |
+
Prilezhaev reaction,https://en.wikipedia.org/wiki/Prilezhaev_reaction
|
633 |
+
Prins reaction,https://en.wikipedia.org/wiki/Prins_reaction
|
634 |
+
Prinzbach synthesis,https://en.wikipedia.org/wiki/Prinzbach_synthesis
|
635 |
+
Protecting group,https://en.wikipedia.org/wiki/Protecting_group
|
636 |
+
Pschorr reaction,https://en.wikipedia.org/wiki/Pschorr_reaction
|
637 |
+
Pummerer rearrangement,https://en.wikipedia.org/wiki/Pummerer_rearrangement
|
638 |
+
PUREX,https://en.wikipedia.org/wiki/PUREX
|
639 |
+
Q[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=18
|
640 |
+
Quelet reaction,https://en.wikipedia.org/wiki/Quelet_reaction
|
641 |
+
R[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=19
|
642 |
+
Ramberg�B�cklund reaction,https://en.wikipedia.org/wiki/Ramberg%E2%80%93B%C3%A4cklund_reaction
|
643 |
+
Raney nickel,https://en.wikipedia.org/wiki/Raney_nickel
|
644 |
+
Rap�Stoermer condensation,https://en.wikipedia.org/wiki/Rap%E2%80%93Stoermer_condensation
|
645 |
+
Raschig phenol process,https://en.wikipedia.org/wiki/Raschig_phenol_process
|
646 |
+
Rauhut�Currier reaction,https://en.wikipedia.org/wiki/Rauhut%E2%80%93Currier_reaction
|
647 |
+
Racemization,https://en.wikipedia.org/wiki/Racemization
|
648 |
+
Reductive amination,https://en.wikipedia.org/wiki/Reductive_amination
|
649 |
+
Reductive dehalogenation of halo ketones,https://en.wikipedia.org/wiki/Reductive_dehalogenation_of_halo_ketones
|
650 |
+
Reed reaction,https://en.wikipedia.org/wiki/Reed_reaction
|
651 |
+
Reilly�Hickinbottom rearrangement,https://en.wikipedia.org/wiki/Reilly%E2%80%93Hickinbottom_rearrangement
|
652 |
+
Reimer�Tiemann reaction,https://en.wikipedia.org/wiki/Reimer%E2%80%93Tiemann_reaction
|
653 |
+
Reissert indole synthesis,https://en.wikipedia.org/wiki/Reissert_indole_synthesis
|
654 |
+
Reppe synthesis,https://en.wikipedia.org/wiki/Reppe_synthesis
|
655 |
+
Retropinacol rearrangement,https://en.wikipedia.org/wiki/Retropinacol_rearrangement
|
656 |
+
Rieche formylation,https://en.wikipedia.org/wiki/Rieche_formylation
|
657 |
+
Riemschneider thiocarbamate synthesis,https://en.wikipedia.org/wiki/Riemschneider_thiocarbamate_synthesis
|
658 |
+
Riley oxidations,https://en.wikipedia.org/wiki/Riley_oxidations
|
659 |
+
Ring closing metathesis,https://en.wikipedia.org/wiki/Olefin_metathesis
|
660 |
+
Ring opening metathesis,https://en.wikipedia.org/wiki/Olefin_metathesis
|
661 |
+
Robinson annulation,https://en.wikipedia.org/wiki/Robinson_annulation
|
662 |
+
Robinson�Gabriel synthesis,https://en.wikipedia.org/wiki/Robinson%E2%80%93Gabriel_synthesis
|
663 |
+
Robinson Schopf reaction,https://en.wikipedia.org/wiki/Robinson_Schopf_reaction
|
664 |
+
Rosenmund reaction,https://en.wikipedia.org/wiki/Rosenmund_reaction
|
665 |
+
Rosenmund reduction,https://en.wikipedia.org/wiki/Rosenmund_reduction
|
666 |
+
Rosenmund�von Braun synthesis,https://en.wikipedia.org/wiki/Rosenmund%E2%80%93von_Braun_synthesis
|
667 |
+
Roskamp reaction,https://en.wikipedia.org/wiki/Roskamp_reaction
|
668 |
+
Rothemund reaction,https://en.wikipedia.org/wiki/Rothemund_reaction
|
669 |
+
Rupe rearrangement,https://en.wikipedia.org/wiki/Rupe_rearrangement
|
670 |
+
Rubottom oxidation,https://en.wikipedia.org/wiki/Rubottom_oxidation
|
671 |
+
Ruff�Fenton degradation,https://en.wikipedia.org/wiki/Ruff%E2%80%93Fenton_degradation
|
672 |
+
Ruzicka large-ring synthesis,https://en.wikipedia.org/wiki/Ruzicka_large-ring_synthesis
|
673 |
+
S[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=20
|
674 |
+
Saegusa�Ito oxidation,https://en.wikipedia.org/wiki/Saegusa%E2%80%93Ito_oxidation
|
675 |
+
Sakurai reaction,https://en.wikipedia.org/wiki/Sakurai_reaction
|
676 |
+
Salol reaction,https://en.wikipedia.org/wiki/Salol_reaction
|
677 |
+
Sandheimer,https://en.wikipedia.org/wiki/Sandheimer
|
678 |
+
Sandmeyer diphenylurea isatin synthesis,https://en.wikipedia.org/wiki/Sandmeyer_diphenylurea_isatin_synthesis
|
679 |
+
Sandmeyer isonitrosoacetanilide isatin synthesis,https://en.wikipedia.org/wiki/Sandmeyer_isonitrosoacetanilide_isatin_synthesis
|
680 |
+
Sandmeyer reaction,https://en.wikipedia.org/wiki/Sandmeyer_reaction
|
681 |
+
Sanger reagent,https://en.wikipedia.org/wiki/Sanger_reagent
|
682 |
+
Saponification,https://en.wikipedia.org/wiki/Saponification
|
683 |
+
Sarett oxidation,https://en.wikipedia.org/wiki/Sarett_oxidation
|
684 |
+
Schiff reaction,https://en.wikipedia.org/wiki/Schiff_base
|
685 |
+
Schiff test,https://en.wikipedia.org/wiki/Schiff_test
|
686 |
+
Schlenk equilibrium,https://en.wikipedia.org/wiki/Schlenk_equilibrium
|
687 |
+
Schlosser modification,https://en.wikipedia.org/wiki/Schlosser_modification
|
688 |
+
Schlosser variant,https://en.wikipedia.org/wiki/Schlosser_variant
|
689 |
+
Schmidlin ketene synthesis,https://en.wikipedia.org/wiki/Schmidlin_ketene_synthesis
|
690 |
+
Schmidt degradation,https://en.wikipedia.org/wiki/Schmidt_degradation
|
691 |
+
Schmidt reaction,https://en.wikipedia.org/wiki/Schmidt_reaction
|
692 |
+
Scholl reaction,https://en.wikipedia.org/wiki/Scholl_reaction
|
693 |
+
Schotten�Baumann reaction,https://en.wikipedia.org/wiki/Schotten%E2%80%93Baumann_reaction
|
694 |
+
Seliwanoff's test,https://en.wikipedia.org/wiki/Seliwanoff%27s_test
|
695 |
+
Semidine rearrangement,https://en.wikipedia.org/wiki/Semidine_rearrangement
|
696 |
+
Semmler�Wolff reaction,https://en.wikipedia.org/wiki/Semmler%E2%80%93Wolff_reaction
|
697 |
+
Seyferth�Gilbert homologation,https://en.wikipedia.org/wiki/Seyferth%E2%80%93Gilbert_homologation
|
698 |
+
Shapiro reaction,https://en.wikipedia.org/wiki/Shapiro_reaction
|
699 |
+
Sharpless asymmetric dihydroxylation,https://en.wikipedia.org/wiki/Sharpless_asymmetric_dihydroxylation
|
700 |
+
Sharpless oxyamination�or aminohydroxylation,https://en.wikipedia.org/wiki/Sharpless_oxyamination
|
701 |
+
Shenck ene reaction,https://en.wikipedia.org/wiki/Ene_reaction
|
702 |
+
Shi epoxidation,https://en.wikipedia.org/wiki/Shi_epoxidation
|
703 |
+
Shiina esterification,https://en.wikipedia.org/wiki/Shiina_esterification
|
704 |
+
Shiina macrolactonization�or Shiina lactonization,https://en.wikipedia.org/wiki/Shiina_macrolactonization
|
705 |
+
Sigmatropic reaction,https://en.wikipedia.org/wiki/Sigmatropic_reaction
|
706 |
+
Simmons�Smith reaction,https://en.wikipedia.org/wiki/Simmons%E2%80%93Smith_reaction
|
707 |
+
Simonini reaction,https://en.wikipedia.org/wiki/Simonini_reaction
|
708 |
+
Simonis chromone cyclization,https://en.wikipedia.org/wiki/Simonis_chromone_cyclization
|
709 |
+
Simons process,https://en.wikipedia.org/wiki/Electrochemical_fluorination
|
710 |
+
Skraup chinolin synthesis,https://en.wikipedia.org/wiki/Skraup_chinolin_synthesis
|
711 |
+
Skraup reaction,https://en.wikipedia.org/wiki/Skraup_reaction
|
712 |
+
Smiles rearrangement,https://en.wikipedia.org/wiki/Smiles_rearrangement
|
713 |
+
SNAr�nucleophilic aromatic substitution,https://en.wikipedia.org/wiki/SNAr
|
714 |
+
SN1,https://en.wikipedia.org/wiki/SN1
|
715 |
+
SN2,https://en.wikipedia.org/wiki/SN2
|
716 |
+
SNi,https://en.wikipedia.org/wiki/SNi
|
717 |
+
Solvolysis,https://en.wikipedia.org/wiki/Solvolysis
|
718 |
+
Sommelet reaction,https://en.wikipedia.org/wiki/Sommelet_reaction
|
719 |
+
Sonn�M�ller method,https://en.wikipedia.org/wiki/Sonn%E2%80%93M%C3%BCller_method
|
720 |
+
Sonogashira coupling,https://en.wikipedia.org/wiki/Sonogashira_coupling
|
721 |
+
S�rensen formol titration,https://en.wikipedia.org/wiki/S%C3%B8rensen_formol_titration
|
722 |
+
Staedel�Rugheimer pyrazine synthesis,https://en.wikipedia.org/wiki/Staedel%E2%80%93Rugheimer_pyrazine_synthesis
|
723 |
+
Stahl oxidation,https://en.wikipedia.org/wiki/Stahl_oxidation
|
724 |
+
Staudinger reaction,https://en.wikipedia.org/wiki/Staudinger_reaction
|
725 |
+
Staudinger synthesis,https://en.wikipedia.org/wiki/Staudinger_synthesis
|
726 |
+
Steglich esterification,https://en.wikipedia.org/wiki/Steglich_esterification
|
727 |
+
Stephen aldehyde synthesis,https://en.wikipedia.org/wiki/Stephen_aldehyde_synthesis
|
728 |
+
Stetter reaction,https://en.wikipedia.org/wiki/Stetter_reaction
|
729 |
+
Stevens rearrangement,https://en.wikipedia.org/wiki/Stevens_rearrangement
|
730 |
+
Stieglitz rearrangement,https://en.wikipedia.org/wiki/Stieglitz_rearrangement
|
731 |
+
Stille coupling,https://en.wikipedia.org/wiki/Stille_coupling
|
732 |
+
Stobbe condensation,https://en.wikipedia.org/wiki/Stobbe_condensation
|
733 |
+
Stoll� synthesis,https://en.wikipedia.org/wiki/Stoll%C3%A9_synthesis
|
734 |
+
Stork acylation,https://en.wikipedia.org/wiki/Stork_acylation
|
735 |
+
Stork enamine alkylation,https://en.wikipedia.org/wiki/Stork_enamine_alkylation
|
736 |
+
Strecker amino acid synthesis,https://en.wikipedia.org/wiki/Strecker_amino_acid_synthesis
|
737 |
+
Strecker degradation,https://en.wikipedia.org/wiki/Strecker_degradation
|
738 |
+
Strecker sulfite alkylation,https://en.wikipedia.org/wiki/Strecker_sulfite_alkylation
|
739 |
+
Strecker synthesis,https://en.wikipedia.org/wiki/Strecker_synthesis
|
740 |
+
"Stereocontrolled 1,2-addition to carbonyl groups","https://en.wikipedia.org/wiki/Stereocontrolled_1,2-addition_to_carbonyl_groups"
|
741 |
+
Suzuki coupling,https://en.wikipedia.org/wiki/Suzuki_coupling
|
742 |
+
Swain equation,https://en.wikipedia.org/wiki/Swain_equation
|
743 |
+
Swarts reaction,https://en.wikipedia.org/wiki/Swarts_reaction
|
744 |
+
Swern oxidation,https://en.wikipedia.org/wiki/Swern_oxidation
|
745 |
+
T[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=21
|
746 |
+
Tamao oxidation,https://en.wikipedia.org/wiki/Tamao_oxidation
|
747 |
+
Tafel rearrangement,https://en.wikipedia.org/wiki/Tafel_rearrangement
|
748 |
+
Takai olefination,https://en.wikipedia.org/wiki/Takai_olefination
|
749 |
+
Tebbe olefination,https://en.wikipedia.org/wiki/Tebbe_olefination
|
750 |
+
ter Meer reaction,https://en.wikipedia.org/wiki/Ter_Meer_reaction
|
751 |
+
Thiele reaction,https://en.wikipedia.org/wiki/Thiele_reaction
|
752 |
+
Thiol-yne reaction,https://en.wikipedia.org/wiki/Thiol-yne_reaction
|
753 |
+
Thorpe reaction,https://en.wikipedia.org/wiki/Thorpe_reaction
|
754 |
+
Tiemann rearrangement,https://en.wikipedia.org/wiki/Tiemann_rearrangement
|
755 |
+
Tiffeneau ring enlargement reaction,https://en.wikipedia.org/wiki/Tiffeneau_ring_enlargement_reaction
|
756 |
+
Tiffeneau�Demjanov rearrangement,https://en.wikipedia.org/wiki/Tiffeneau%E2%80%93Demjanov_rearrangement
|
757 |
+
Tischtschenko reaction,https://en.wikipedia.org/wiki/Tischtschenko_reaction
|
758 |
+
Tollens reagent,https://en.wikipedia.org/wiki/Tollens_reagent
|
759 |
+
Transfer hydrogenation,https://en.wikipedia.org/wiki/Transfer_hydrogenation
|
760 |
+
Trapp mixture,https://en.wikipedia.org/wiki/Trapp_mixture
|
761 |
+
Transesterification,https://en.wikipedia.org/wiki/Transesterification
|
762 |
+
Traube purine synthesis,https://en.wikipedia.org/wiki/Traube_purine_synthesis
|
763 |
+
Truce�Smiles rearrangement,https://en.wikipedia.org/wiki/Truce%E2%80%93Smiles_rearrangement
|
764 |
+
Tscherniac�Einhorn reaction,https://en.wikipedia.org/wiki/Tscherniac%E2%80%93Einhorn_reaction
|
765 |
+
Tschitschibabin reaction,https://en.wikipedia.org/wiki/Tschitschibabin_reaction
|
766 |
+
Tschugajeff reaction,https://en.wikipedia.org/wiki/Chugaev_reaction
|
767 |
+
Tsuji�Trost reaction,https://en.wikipedia.org/wiki/Tsuji%E2%80%93Trost_reaction
|
768 |
+
Tsuji�Wilkinson decarbonylation reaction,https://en.wikipedia.org/wiki/Tsuji%E2%80%93Wilkinson_decarbonylation_reaction
|
769 |
+
Twitchell process,https://en.wikipedia.org/wiki/Twitchell_process
|
770 |
+
Tyrer sulfonation process,https://en.wikipedia.org/wiki/Tyrer_sulfonation_process
|
771 |
+
U[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=22
|
772 |
+
Ugi reaction,https://en.wikipedia.org/wiki/Ugi_reaction
|
773 |
+
Ullmann reaction,https://en.wikipedia.org/wiki/Ullmann_reaction
|
774 |
+
Upjohn dihydroxylation,https://en.wikipedia.org/wiki/Upjohn_dihydroxylation
|
775 |
+
Urech cyanohydrin method,https://en.wikipedia.org/wiki/Urech_cyanohydrin_method
|
776 |
+
Urech hydantoin synthesis,https://en.wikipedia.org/wiki/Urech_hydantoin_synthesis
|
777 |
+
V[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=23
|
778 |
+
Van Leusen reaction,https://en.wikipedia.org/wiki/Van_Leusen_reaction
|
779 |
+
Van Slyke determination,https://en.wikipedia.org/wiki/Van_Slyke_determination
|
780 |
+
Varrentrapp reaction,https://en.wikipedia.org/wiki/Varrentrapp_reaction
|
781 |
+
Vilsmeier reaction,https://en.wikipedia.org/wiki/Vilsmeier_reaction
|
782 |
+
Vilsmeier�Haack reaction,https://en.wikipedia.org/wiki/Vilsmeier%E2%80%93Haack_reaction
|
783 |
+
Voight amination,https://en.wikipedia.org/wiki/Voight_amination
|
784 |
+
Volhard�Erdmann cyclization,https://en.wikipedia.org/wiki/Volhard%E2%80%93Erdmann_cyclization
|
785 |
+
von Braun amide degradation,https://en.wikipedia.org/wiki/Von_Braun_amide_degradation
|
786 |
+
von Braun reaction,https://en.wikipedia.org/wiki/Von_Braun_reaction
|
787 |
+
von Richter cinnoline synthesis,https://en.wikipedia.org/wiki/Von_Richter_cinnoline_synthesis
|
788 |
+
von Richter reaction,https://en.wikipedia.org/wiki/Von_Richter_reaction
|
789 |
+
W[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=24
|
790 |
+
Wacker�Tsuji oxidation,https://en.wikipedia.org/wiki/Wacker%E2%80%93Tsuji_oxidation
|
791 |
+
Wagner-Jauregg reaction,https://en.wikipedia.org/wiki/Wagner-Jauregg_reaction
|
792 |
+
Wagner�Meerwein rearrangement,https://en.wikipedia.org/wiki/Wagner%E2%80%93Meerwein_rearrangement
|
793 |
+
Waits�Scheffer epoxidation,https://en.wikipedia.org/wiki/Waits%E2%80%93Scheffer_epoxidation
|
794 |
+
Walden inversion,https://en.wikipedia.org/wiki/Walden_inversion
|
795 |
+
Wallach rearrangement,https://en.wikipedia.org/wiki/Wallach_rearrangement
|
796 |
+
Weerman degradation,https://en.wikipedia.org/wiki/Weerman_degradation
|
797 |
+
Weinreb ketone synthesis,https://en.wikipedia.org/wiki/Weinreb_ketone_synthesis
|
798 |
+
Wenker ring closure,https://en.wikipedia.org/wiki/Wenker_ring_closure
|
799 |
+
Wenker synthesis,https://en.wikipedia.org/wiki/Wenker_synthesis
|
800 |
+
Wessely�Moser rearrangement,https://en.wikipedia.org/wiki/Wessely%E2%80%93Moser_rearrangement
|
801 |
+
Westphalen�Lettr� rearrangement,https://en.wikipedia.org/wiki/Westphalen%E2%80%93Lettr%C3%A9_rearrangement
|
802 |
+
Wharton reaction,https://en.wikipedia.org/wiki/Wharton_reaction
|
803 |
+
Whiting reaction,https://en.wikipedia.org/wiki/Whiting_reaction
|
804 |
+
Wichterle reaction,https://en.wikipedia.org/wiki/Wichterle_reaction
|
805 |
+
Widman�Stoermer synthesis,https://en.wikipedia.org/wiki/Widman%E2%80%93Stoermer_synthesis
|
806 |
+
Wilkinson catalyst,https://en.wikipedia.org/wiki/Wilkinson_catalyst
|
807 |
+
Willgerodt rearrangement,https://en.wikipedia.org/wiki/Willgerodt_rearrangement
|
808 |
+
Willgerodt�Kindler reaction,https://en.wikipedia.org/wiki/Willgerodt%E2%80%93Kindler_reaction
|
809 |
+
Williamson ether synthesis,https://en.wikipedia.org/wiki/Williamson_ether_synthesis
|
810 |
+
Winstein reaction,https://en.wikipedia.org/wiki/Winstein_reaction
|
811 |
+
Wittig reaction,https://en.wikipedia.org/wiki/Wittig_reaction
|
812 |
+
"1,2-Wittig rearrangement","https://en.wikipedia.org/wiki/1,2-Wittig_rearrangement"
|
813 |
+
"2,3-Wittig rearrangement","https://en.wikipedia.org/wiki/2,3-Wittig_rearrangement"
|
814 |
+
Wittig�Horner reaction,https://en.wikipedia.org/wiki/Wittig%E2%80%93Horner_reaction
|
815 |
+
Wohl degradation,https://en.wikipedia.org/wiki/Wohl_degradation
|
816 |
+
Wohl�Aue reaction,https://en.wikipedia.org/wiki/Wohl%E2%80%93Aue_reaction
|
817 |
+
Wohler synthesis,https://en.wikipedia.org/wiki/Wohler_synthesis
|
818 |
+
Wohl�Ziegler reaction,https://en.wikipedia.org/wiki/Wohl%E2%80%93Ziegler_reaction
|
819 |
+
Wolffenstein�B�ters reaction,https://en.wikipedia.org/wiki/Wolffenstein%E2%80%93B%C3%B6ters_reaction
|
820 |
+
Wolff rearrangement,https://en.wikipedia.org/wiki/Wolff_rearrangement
|
821 |
+
Wolff�Kishner reduction,https://en.wikipedia.org/wiki/Wolff%E2%80%93Kishner_reduction
|
822 |
+
Woodward cis-hydroxylation,https://en.wikipedia.org/wiki/Woodward_cis-hydroxylation
|
823 |
+
Woodward�Hoffmann rule,https://en.wikipedia.org/wiki/Woodward%E2%80%93Hoffmann_rule
|
824 |
+
Wulff�D�tz reaction,https://en.wikipedia.org/wiki/Wulff%E2%80%93D%C3%B6tz_reaction
|
825 |
+
Wurtz�Fittig reaction,https://en.wikipedia.org/wiki/Wurtz%E2%80%93Fittig_reaction
|
826 |
+
Y[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=25
|
827 |
+
Yamada�Okamoto purine synthesis,https://en.wikipedia.org/wiki/Purine
|
828 |
+
Yamaguchi esterification,https://en.wikipedia.org/wiki/Yamaguchi_esterification
|
829 |
+
Z[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=26
|