人名反应

A

• Acetoacetic Ester synthesis
• Acyloin Condensation
• Alder-Ene Reaction
• Aldol Addition
• Aldol Addition
• Alkene metathesis
• Alkyne metathesis
• Amadori reaction/rearrangement
• Appel Reaction
• Arbuzov Reaction
• Arndt-Eistert Synthesis
• aza-[2,3]-Wittig rearrangement
• aza-Claisen rearrangement
• aza-Cope rearrangement
• aza Wittig reaction
• Azide-Alkyne 1,3-Dipolar Cycloaddition
• Azo Coupling

B

• Baeyer-Villiger oxidation
• Baker-Venkataraman rearrangement
• Baldwin rules
• Balz-Schiemann reaction
• Bamford-Stevens reaction
• Barbier reaction
• Barroli indole synthesis
• Barton-McCombie reaction
• Barton nitrite ester reaction
• Baylis-Hillman reaction
• Beckmann rearrangement
• Benzilic acid rearrangement
• Benzoin condensation
• Bergman cyclization
• Bestmann-Ohira reagent
• Biginelli reaction
• Birch reduction
• Bischler-Napieralski reaction
• Blaise reaction
• Blanc reaction
• Bohlmann-Rahtz pyridine synthesis
• Boronic acid Mannich reaction
• Bouveault-Blanc reduction
• Brook rearrangement
• Brown hydroboration
• Buchner ring expansion
• Bucherer-Bergs reaction
• Buchwald-Hartwig cross coupling reaction
• Burgess dehydration reaction

C

• Cadiot-Chodkiewicz coupling
• Cannizzaro oxidation-reduction
• Carroll rearrangement
• Castro-Stephens Coupling
• CBS reduction
• Chan-Lam coupling
• Chichibabin reaction
• Chugaev elimination reaction
• Ciamician Dennstedt Rearrangement
• Claisen condensation
• Claisen rearrangement
• Clemmensen reduction
• Click chemistry
• Collins reagent
• Combes Quinoline Synthesis
• Cope elimination
• Cope rearrangement
• Conia-Ene reaction
• Corey-Bakshi-Shibata reduction
• Corey-Chaykovsky reaction
• Corey-Fuchs reaction
• Corey-Kim oxidation
• Corey-Seebach reaction
• Corey-Suggs reagent
• Corey-Winter olefin synthesis
• Corey Nicolaou Macrolactonization
• Cornforth Rearrangement
• Coumarin synthesis
• Criegee mechanism for ozonolysis
• Cross metathesis
• Curtius rearrangement (reaction)

D

• Dakin reaction
• Dakin West reaction
• Danheiser benzannulation
• Danheiser cyclopentene annulation
• Danishefsky Diene Cycloadditions
• Darzens condensation
• Darzens reaction
• Davis oxaziridine oxidation
• Davis oxidation
• De Kimpe aziridine synthesis
• De Mayo cycloaddition
• Delépine reaction
• Demyanov rearrangement
• Dess-Martin oxidation
• Diazotisation
• Dieckmann condensation
• Diels-Alder reaction
• Dienone phenol rearrangement
• 1,3-dipolar cycloaddition
• Dimroth Rearangement
• Directed ortho metalation
• Doebner modification
• Doering Laflamme Allene_synthesis
• Dotz Benzannulation Reaction

E

• Eglinton reaction
• Enders Samp Ramp Hydrozone_alkylation
• Ene reaction
• Enyne metathesis
• Epoxidation
• Eschenmoser Claisen Rearrangement
• Eschenmoser Methenylation
• Eschenmoser Tanabe Fragmentation
• Eschweiler-Clarke reaction
• Ester pyrolysis
• Esterification
• Evans Aldol Reaction

F

• Favorskii reaction
• Feist Bénary Furan Synthesis
• Ferrier Reaction
• Finkelstein reaction
• Fischer esterification
• Fischer indole synthesis
• Fleming-Tamao oxidation
• Friedel-Crafts acylation
• Friedel-Crafts alkylation
• Friedlaender synthesis
• Fries rearrangement
• Fukuyama coupling
• Fukuyama reduction

G

• Gabriel synthesis
• Gattermann Koch Reaction
• Gewald reaction
• Glaser coupling
• Griesbaum coozonolysis
• Grignard reaction
• Grobe Fragmentation
• Grubbs reaction

H

• Hajos-Parrish reaction
• Haloform reaction
• Hantzsch dihydropyridine synthesis (pyridine synthesis)
• Hay coupling
• Heck reaction
• Heine reaction
• Hell-Volhard-Zelinsky reaction
• Henry reaction
• Hetero Diels-Alder Cycloaddition
• Hiyama coupling
• Hiyama-Denmark coupling
• Hofmann elimination
• Hofmann rearrangement
• Hofmann's rule
• Hofmann Loffler Freytag reaction
• Horner-Wadsworth-Emmons reaction
• Still Gennari modification HWE
• Hosomi-Sakurai reaction
• Houben Hoesch Reaction
• Huisgen cycloaddition
• Hunsdiecker reaction
• Hydroboration

I

• Ireland-Claisen rearrangement
• Itsuno-Corey reduction
• Iwanow reaction (reagent)

J

• Jacobsen epoxidation
• Jacobsen-Katsuki epoxidation
• Jocic reaction
• Johnson-Corey-Chaykovsky reaction
• Jones oxidation
• Julia-Lythgoe olefination
• Julia-Kocienski olefination

K

• Kabachnik-Fields reaction
• Kindler reaction
• Knoevenagel condensation
• Kochi reaction
• Kolbe electrolysis
• Kolbe nitrile synthesis
• Kolbe-Schmitt reaction
• Koser's reagent
• Kowalski ester homologation
• Kulinkovich reaction
• Kulinkovich-de Meijere reaction
• Kulinkovich-Szymoniak reaction
• Kumada coupling

L

• Lawesson's reagent
• Leuckart thiophenol reaction
• Luche reduction

M

• Malonic ester synthesis
• Mannich reaction
• Markovnikov's rule
• McMurry reaction
• Meerwein-Ponndorf-Verley reduction
• Myers' modification of the Ramberg-Bäcklund reaction
• Myers-Saito cyclization
• Michael addition
• Michaelis-Arbuzov reaction
• Mitsunobu reaction
• Miyaura borylation reaction
• Modified Julia olefination
• Mukaiyama aldol addition

N

• Nazarov cyclization
• Nef reaction
• Negishi coupling
• Newman-Kwart rearrangement
• Nitroaldol reaction
• Nozaki-Hiyama coupling
• Nucleophilic substitution (SN1 SN2)

O

• O'Donnell amino acid synthesis
• Ohira-Bestmann reagent
• Olefin metathesis
• Oppenauer oxidation
• Overman rearrangement
• Oxy-Cope rearrangement
• Ozonolysis

P

• Paal-Knorr furan synthesis
• Paal-Knorr pyrrole synthesis
• Paal-Knorr thiophene synthesis
• Passerini reaction
• Paterno-Büchi reaction
• Pauson-Khand reaction
• Pechmann condensation
• Petasis reaction
• Peterson olefination
• Pinacol coupling reaction
• Pinacol rearrangement
• Pinner reaction
• Prévost reaction
• Prilezhaev reaction
• Prins reaction
• Pschorr reaction

Q

R

• Ramberg-Bäcklund reaction
• Reformatsky reaction
• Ring closing metathesis
• Ring opening metathesis (polymerization)
• Ritter reaction
• Robinson annulation
• Rosenmund reduction
• Rosenmund-von Braun reaction
• Rubottom oxidation

S

• Sakurai reaction
• Sandmeyer reaction
• Saytzeff's rule
• Schiemann reaction
• Schlosser modification
• Schmidt reaction
• Schotten-Baumann reaction
• Seebach umpolung
• Seyferth-Gilbert homologation
• Sarett reagent
• Shapiro reaction
• Sharpless aminohydroxylation
• Sharpless dihydroxylation
• Sharpless epoxidation
• Shi epoxidation
• Simmons-Smith reaction
• Sonogashira coupling
• Staudinger cycloaddition
• Staudinger reaction
• Staudinger reduction
• Staudinger synthesis
• Steglich esterification
• Stetter reaction
• Stille coupling
• Strecker synthesis
• Suzuki coupling
• Swern oxidation

T

• Tamao-Kumada oxidation
• Tebbe olefination
• Tishchenko reaction
• Tsuji-Trost reaction
• Trost allylation

U

• Ugi reaction
• Ullmann reaction
• Upjohn dihydroxylation

V

• Van Leusen imidazole synthesis
• Van Leusen oxazole synthesis
• Van Leusen reaction
• Vicarious nucleophilic substitution
• Vilsmeier reaction

W

• Wacker-Tsuji oxidation
• Weinreb ketone synthesis
• Wenker synthesis
• Willgerodt-Kindler reaction
• Williamson synthesis
• Wittig-Horner reaction
• Wittig reaction
• [1,2]-Wittig rearrangement
• [2,3]-Wittig rearrangement
• Wohl-Ziegler reaction
• Wolff-Kishner reduction
• Wolff rearrangement
• Woodward cis-hydroxylation
• Woodward reaction
• Wurtz reaction
• Wurtz-Fittig reaction

X

Y

• Yamaguchi esterification

Z