name
stringlengths 1
52
| link
stringlengths 31
118
|
|---|---|
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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