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Name Reactions

文字:[大][中][小] 手机页面二维码 2016/12/7    浏览次数:    


Name Reactions


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Product of the Month

a b c d e f g h i j k l m n o p q r s t u v w x y z


 a

Acetoacetic Ester Condensation

Acetoacetic Ester Synthesis

Acyloin Condensation

Alder-Ene Reaction

Aldol Addition

Aldol Condensation

Appel Reaction

Arbuzov Reaction

Arndt-Eistert Synthesis

Azide-Alkyne 1,3-Dipolar Cycloaddition

Azo Coupling

 b

Baeyer-Villiger Oxidation

Baker-Venkataraman Rearrangement

Balz-Schiemann Reaction

Bamford-Stevens Reaction

Barton Decarboxylation

Barton-McCombie Reaction (Barton Desoxygenation)

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

Bucherer-Bergs Reaction

Buchwald-Hartwig Cross Coupling Reaction

 c

Cadiot-Chodkiewicz Coupling

Cannizzaro Oxidation Reduction

CBS Reduction

Chan-Lam Coupling

Claisen Condensation

Claisen Rearrangement

Clemmensen Reduction

Click Chemistry

Collins Reagent

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

Coumarin Synthesis

Criegee Mechanism for Ozonolysis

Cross Metathesis

Curtius Rearrangement (Reaction)

 d

Dakin Reaction

Darzens Condensation

Darzens Reaction

De Kimpe Aziridine Synthesis

Delépine Reaction

Dess-Martin Oxidation

Diazotisation

Dieckmann Condensation

Diels-Alder Reaction

1,3-Dipolar Cycloaddition

Directed ortho Metalation

Doebner Modification

 e

Eglinton Reaction

Ene Reaction

Enyne Metathesis

Epoxidation

Eschweiler-Clarke Reaction

Ester Pyrolysis

Esterification

 f

Favorskii 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

Gewald Reaction

Glaser Coupling

Griesbaum Coozonolysis

Grignard Reaction

Grubbs Reaction

 h

Haloform Reaction

Hantzsch Dihydropyridine Synthesis (Pyridine Synthesis)

Hay Coupling

Heck Reaction

Hell-Volhard-Zelinsky Reaction

Henry Reaction

Hiyama Coupling

Hiyama-Denmark Coupling

Hofmann Elimination

Hofmann's Rule

Horner-Wadsworth-Emmons Reaction

Hosomi-Sakurai 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

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

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


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