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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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=26