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appel-reaction | https://www.name-reaction.com/appel-reaction |
baeyer-villiger-oxidation | https://www.name-reaction.com/baeyer-villiger-oxidation |
bartoli-indole-synthesis | https://www.name-reaction.com/bartoli-indole-synthesis |
baylis-hillman-reaction | https://www.name-reaction.com/baylis-hillman-reaction |
beckmann-rearrangement | https://www.name-reaction.com/beckmann-rearrangement |
biginelli-reaction | https://www.name-reaction.com/biginelli-reaction |
birch-reduction | https://www.name-reaction.com/birch-reduction |
buchwald-hartwig-amination | https://www.name-reaction.com/buchwald-hartwig-amination |
cannizzaro-reaction | https://www.name-reaction.com/cannizzaro-reaction |
claisen-condensation | https://www.name-reaction.com/claisen-condensation |
claisen-rearrangement | https://www.name-reaction.com/claisen-rearrangement |
clemmensen-reduction | https://www.name-reaction.com/clemmensen-reduction |
cope-rearrangement | https://www.name-reaction.com/cope-rearrangement |
corey-kim-oxidation | https://www.name-reaction.com/corey-kim-oxidation |
curtius-rearrangement | https://www.name-reaction.com/curtius-rearrangement |
dakin-west-reaction | https://www.name-reaction.com/dakin-west-reaction |
dieckmann-condensation | https://www.name-reaction.com/dieckmann-condensation |
diels-alder-reaction | https://www.name-reaction.com/diels-alder-reaction |
eschenmoser-claisen-rearrangement | https://www.name-reaction.com/eschenmoser-claisen-rearrangement |
eschweiler-clarke-reaction | https://www.name-reaction.com/eschweiler-clarke-reaction |
finkelstein-reaction | https://www.name-reaction.com/finkelstein-reaction |
fischer-esterification | https://www.name-reaction.com/fischer-esterification |
fischer-indole-synthesis | https://www.name-reaction.com/fischer-indole-synthesis |
friedel-crafts-acylation | https://www.name-reaction.com/friedel-crafts-acylation |
friedel-crafts-alkylation | https://www.name-reaction.com/friedel-crafts-alkylation |
fries-rearrangement | https://www.name-reaction.com/fries-rearrangement |
gabriel-synthesis | https://www.name-reaction.com/gabriel-synthesis |
grignard-reaction | https://www.name-reaction.com/grignard-reaction |
heck-reaction | https://www.name-reaction.com/heck-reaction |
hell-volhard-zelinsky-reaction | https://www.name-reaction.com/hell-volhard-zelinsky-reaction |
henry-reaction | https://www.name-reaction.com/henry-reaction |
hofmann-elimination | https://www.name-reaction.com/hofmann-elimination |
hofmann-rearrangement | https://www.name-reaction.com/hofmann-rearrangement |
ireland-claisen-rearrangement | https://www.name-reaction.com/ireland-claisen-rearrangement |
johnson-claisen-rearrangement | https://www.name-reaction.com/johnson-claisen-rearrangement |
jones-oxidation | https://www.name-reaction.com/jones-oxidation |
knoevenagel-condensation | https://www.name-reaction.com/knoevenagel-condensation |
knorr-pyrazole-synthesis | https://www.name-reaction.com/knorr-pyrazole-synthesis |
kolbe-schmitt-reaction | https://www.name-reaction.com/kolbe-schmitt-reaction |
kumada-cross-coupling | https://www.name-reaction.com/kumada-cross-coupling |
luche-reduction | https://www.name-reaction.com/luche-reduction |
mannich-reaction | https://www.name-reaction.com/mannich-reaction |
michael-addition | https://www.name-reaction.com/michael-addition |
mitsunobu-reaction | https://www.name-reaction.com/mitsunobu-reaction |
mukaiyama-aldol-addition | https://www.name-reaction.com/mukaiyama-aldol-addition |
n | https://www.name-reaction.com/n |
negishi-cross-coupling | https://www.name-reaction.com/negishi-cross-coupling |
oppenauer-oxidation | https://www.name-reaction.com/oppenauer-oxidation |
pauson-khand-reaction | https://www.name-reaction.com/pauson-khand-reaction |
perkin-reaction | https://www.name-reaction.com/perkin-reaction |
pictet-spengler-reaction | https://www.name-reaction.com/pictet-spengler-reaction |
prins-reaction | https://www.name-reaction.com/prins-reaction |
reformatsky-reaction | https://www.name-reaction.com/reformatsky-reaction |
reimer-tiemann-reaction | https://www.name-reaction.com/reimer-tiemann-reaction |
ritter-reaction | https://www.name-reaction.com/ritter-reaction |
robinson-annulation | https://www.name-reaction.com/robinson-annulation |
sandmeyer-reaction | https://www.name-reaction.com/sandmeyer-reaction |
schmidt-reaction | https://www.name-reaction.com/schmidt-reaction |
schotten-baumann-reaction | https://www.name-reaction.com/schotten-baumann-reaction |
sharpless-epoxidation | https://www.name-reaction.com/sharpless-epoxidation |
sonogashira-cross-coupling | https://www.name-reaction.com/sonogashira-cross-coupling |
staudinger-reaction | https://www.name-reaction.com/staudinger-reaction |
stille-cross-coupling | https://www.name-reaction.com/stille-cross-coupling |
strecker-amino-acid-synthesis | https://www.name-reaction.com/strecker-amino-acid-synthesis |
suzuki-cross-coupling | https://www.name-reaction.com/suzuki-cross-coupling |
swern-oxidation | https://www.name-reaction.com/swern-oxidation |
ullmann-reaction | https://www.name-reaction.com/ullmann-reaction |
vilsmeier-haack-reaction | https://www.name-reaction.com/vilsmeier-haack-reaction |
wagner-meerwein-rearrangement | https://www.name-reaction.com/wagner-meerwein-rearrangement |
williamson-ether-synthesis | https://www.name-reaction.com/williamson-ether-synthesis |
wittig-reaction | https://www.name-reaction.com/wittig-reaction |
wolff-rearrangement | https://www.name-reaction.com/wolff-rearrangement |
wolff-kishner-reduction | https://www.name-reaction.com/wolff-kishner-reduction |
wurtz-reaction | https://www.name-reaction.com/wurtz-reaction |
yamaguchi-esterification | https://www.name-reaction.com/yamaguchi-esterification |
0-9[edit] | https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=1 |
1,2-Wittig rearrangement | https://en.wikipedia.org/wiki/1,2-Wittig_rearrangement |
1,3-Dipolar cycloaddition | https://en.wikipedia.org/wiki/1,3-Dipolar_cycloaddition |
2,3-Wittig rearrangement | https://en.wikipedia.org/wiki/2,3-Wittig_rearrangement |
A[edit] | https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=2 |
Abramovitch�Shapiro tryptamine synthesis | https://en.wikipedia.org/wiki/Tryptamine |
Acetalisation | https://en.wikipedia.org/wiki/Acetalisation |
Acetoacetic ester condensation | https://en.wikipedia.org/wiki/Acetoacetic_ester_condensation |
Achmatowicz reaction | https://en.wikipedia.org/wiki/Achmatowicz_reaction |
Acylation | https://en.wikipedia.org/wiki/Acylation |
Acyloin condensation | https://en.wikipedia.org/wiki/Acyloin_condensation |
Adams' catalyst | https://en.wikipedia.org/wiki/Adams%27_catalyst |
Adams decarboxylation | https://en.wikipedia.org/wiki/Adams_decarboxylation |
Adkins catalyst | https://en.wikipedia.org/wiki/Adkins_catalyst |
Adkins�Peterson reaction | https://en.wikipedia.org/wiki/Adkins%E2%80%93Peterson_reaction |
Akabori amino acid reaction | https://en.wikipedia.org/wiki/Akabori_amino_acid_reaction |
Alcohol oxidation | https://en.wikipedia.org/wiki/Alcohol_oxidation |
Alder�Stein rules | https://en.wikipedia.org/wiki/Alder%E2%80%93Stein_rules |
Aldol addition | https://en.wikipedia.org/wiki/Aldol_addition |
Aldol condensation | https://en.wikipedia.org/wiki/Aldol_condensation |
Algar�Flynn�Oyamada reaction | https://en.wikipedia.org/wiki/Algar%E2%80%93Flynn%E2%80%93Oyamada_reaction |
Alkylimino-de-oxo-bisubstitution | https://en.wikipedia.org/wiki/Alkylimino-de-oxo-bisubstitution |
Alkyne trimerisation | https://en.wikipedia.org/wiki/Alkyne_trimerisation |
Alkyne zipper reaction | https://en.wikipedia.org/wiki/Alkyne_zipper_reaction |
Allan�Robinson reaction | https://en.wikipedia.org/wiki/Allan%E2%80%93Robinson_reaction |
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