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Name reactions, organic reactions



Name reactions

A name reaction is an chemical reaction named after its discoverer.

Online available information resources on name reactions and reaction mechanisms in chemistry.

Further information categories about related topics are listed in the navigation menu on the left side of these page.



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Acetoacetic Ester Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Acetoacetic Ester Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Acid catalysed hydrolysis of esters . . .
Detail at the mechanism for the hydrolysis of esters in the presence of a dilute acid (such as hydrochloric acid or sulphuric acid) acting as the catalyst. Chemguide - [e]

Acyloin Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Alder-Ene Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Aldol Addition
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Aldol Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Appel Reaction
… converts an alcohol to an alkyl halide - [e]

Appel Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Arbuzov Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Arndt-Eistert Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Azo Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Baeyer-Villiger Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Baeyer-Villiger Oxidation
Baeyer-Villiger Rearrangement - [e]

Baker-Venkataraman Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Balz-Schiemann Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Bamford-Stevens Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Barton-McCombie Reaction (Barton Desoxigenation)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Baylis-Hillman Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Beckmann Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Benzilic Acid Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Benzoin Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Biginelli Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Birch Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Bischler-Napieralski Reaction
Synthesis of 3,4-dihydroisoquinolines from the beta-ethylamides. Organic Chemistry Portal - [d, e]

Blaise Reaction
Synthesis of ß-enamino esters or ß-keto esters via the zinc-mediated reaction of nitriles with a-haloesters. Organic Chemistry Portal - [d, e]

Blanc Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Bouveault-Blanc Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Brook Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Brown Hydroboration
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Bucherer-Bergs Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Buchwald-Hartwig Chemistry
Historical context; development of initial catalytic systems; mechanistic studies and rational design; reaction scope - Format: PDF - [e]

Buchwald-Hartwig Cross Coupling Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Cadiot-Chodkiewicz Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Cannizaro Oxidation Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

CBS Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Chan-Lam Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Claisen Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Claisen Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Clemmensen Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Conia-Ene Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Cope Elimination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Cope Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Corey-Bakshi-Shibata Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Corey-Fuchs Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Corey-Kim Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Corey-Winter Olefin Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Coumarin Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Cross Metathesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Curtius Rearrangement (Reaction)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Dakin Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Dakin West Reaction
… converts an amino acid and an anhydride to an acylamino ketone - [e]

Dess-Martin Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Diazotation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Dieckmann Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Diels-Alder Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Directed ortho Metalation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Doebner Modification
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Eglinton Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Ene Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Epoxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Eschweiler-Clarke Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Ester Pyrolysis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Esterification reaction
Detail at the mechanism for the formation of esters from carboxylic acids and alcohols in the presence of concentrated sulphuric acid acting as the catalyst. Chemguide - [e]

Favorskii Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Finkelstein Reaction
An alkyl halide is converted into another alkyl halide - [e]

Fischer Esterification
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Fischer Indole Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Fischer Tropsch Reaction
The Molecular Basis of the Fischer Tropsch Reaction. Dissertation, 2002 - Format: PDF - [e]

Friedel-Crafts Acylation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Friedel-Crafts Alkylation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Friedlaender Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Fries Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Fukuyama Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Gabriel Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Gewald Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Glaser Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Grignard Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Grubbs Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Haloform Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Hantzsch Dihydropyridine Synthesis (Pyridine Synthesis)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Hay Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Heck Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Hell-Volhard-Zelinsky Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Henry Reaktion
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Hofmann Elimination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Hofmann Rearrangement
… converts a primary amide to a primary amine - [e]

Hofmann's Rule
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Horner-Wadsworth-Emmons Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Hosomi-Sakurai Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Hunsdiecker Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Hydration of ethene to make ethanol
The mechanism for the hydration of ethene to make ethanol using phosphoric(V) acid as the catalyst. Chemguide - [e]

Hydroboration
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Ireland-Claisen Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Iwanow Reaction (Reagent)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Jones Oxidation
… oxidizes alcohols using chromic trioxide and acid in water - [e]

Julia Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Julia Olefination, modified
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Julia-Kocienski Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Julia-Lythgoe Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Kabachnik-Fields Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Kindler Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Knoevenagel Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Kochi Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Kolbe Electrolysis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Kolbe-Schmitt Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Kumada Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Lawesson’s Reagent
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Leuckart Thiophenol Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Luche Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Malonic Ester Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Mannich Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Markovnikov's Rule
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Markovnikov's Rule
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

McMurry Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Meerwein-Ponndorf-Verley Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Michael Addition
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Michaelis-Arbuzov Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Mitsunobu Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Modified Julia Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Mukaiyama Aldol Addition
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Multicomponent Reactions
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Nef Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Nef Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Negishi Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Newman-Kwart Rearrangement
In the NKR a intramolecular aryl migration of O-thiocarbamates at high temperatures leads to S-thiocarbamates. Organic Chemistry Portal - [d, e]

Nitroaldol Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Nozaki-Hiyama Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Olefin Metathesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Olefin Metathesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Oppenauer Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Organosilicon Reactions
Named Organosilicon Reactions - Format: PDF - [e]

Overman Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Oxy-Cope Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Paal-Knorr Furan Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Paal-Knorr Pyrrole Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Paal-Knorr Thiophene Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Passerini Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Paterno-Büchi Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Pauson-Khand Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Pechmann Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Perkin Reaction
Perkin Condensation - [e]

Peterson Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Pictet-Spengler Reaction
Pictet-Spengler tetrahydroisoquinoline synthesis - [e]

Pinacol Coupling Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Pinacol Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Pinner Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Prilezhaev Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Prins Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Pschorr Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Reformatsky Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Reimer-Tiemann Reaction
… converts a phenol to an o-hydroxy benzaldehyde - [e]

Ring Opening Metathesis (Polymerization)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Ritter Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Robinson Anellation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Rosenmund Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Rubottom Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Sakurai Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Sandmeyer Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Saytzeff's Rule
Description and mechanism. Organic Chemistry Portal - [d, e]

Schiemann Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Schlosser Modification
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Schmidt Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Schotten-Baumann Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Shapiro Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Sharpless Epoxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Simmons-Smith Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Sonogashira Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Staudinger Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Steglich Esterification
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Stetter Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Stille Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Strecker Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Suzuki Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Swern Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Tebbe Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Tishhenko Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Tusji-Trost Allylation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Ugi Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Ullmann Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Upjohn Dihydroxylation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Vilsmeier Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wacker-Tsuji Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wagner-Meerwein Rearrangement
… converts an alcohol to an olefin - [e]

Weinreb Ketone Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wenker Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Willgerodt-Kindler Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Williamson Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wittig Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wittig: [1,2]-Wittig Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wittig: [2,3]-Wittig Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wittig-Horner Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wohl-Ziegler Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wolff Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wolff-Kishner Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wurtz Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Wurtz-Fittig Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal - [d, e]

Yamaguchi Esterification
… converts a carboxylic acid and an alcohol to an ester - [e]



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Other Directories


Named Reactions
Named Reactions in Organic Chemistry - [e]

Named Reactions
Named Reactions without mechanisms - [e]

Name-Reaction.com
Comprehensive and visually dynamic, Name-Reaction.com is a tool to quickly and easily learn organic reactions. Name-Reaction.com provides clear and concise reaction schematics and mechanisms that students can easily understand.
Name-Reaction.com is aimed at educating chemists on organic reactions in an interactive, dynamic and easy to understand format in order to better visualize the abstract world of chemistry and facilitate learning. - [e]







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Citation:
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Entries:
201
Topic:
Name reactions, organic reactions
Keywords:
Name reactions, mechanism, organic, chemistry
Update:
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27.01.2013 [site update]


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Related Books and Scientific Literature: Name reactions:


Buchempfehlung

Jie Jack Li, E. J. Corey

Name Reactions of Functional Group Transformations

Unlike many previous books on name reactions, which present many reactions but treat them superficially, this book provides an excellent selection of useful name reactions, which have been given in depth, well-illustrated, instructional, and well-referenced accounts.

Wiley; 2007


Buchempfehlung

Jie Jack Li

Name Reactions: A Collection of Detailed Reaction Mechanisms

The third edition contains major improvements over the previous edition. In addition to updated references, each reaction is now supplemented with two to three representative examples in synthesis to showcase its synthetic utility. Biographical sketches for the chemists who discovered or developed those name reactions have been included. Furthemore, the subject index is significantly expanded.

Different from other books on name reactions in organic chemistry, Name Reactions, A Collection of Detailed Reaction Mechanisms focuses on their mechanisms. It covers over 300 classical as well as contemporary name reactions. Each reaction is delineated by its detailed step-by-step, electron-pushing mechanism, supplemented with the original and the latest references, especially review articles. Thus, it is not only an indispensable resource for senior undergraduate and graduate students for learning and exams, but also a good reference book for all chemists interested in name reactions.

Springer; 2006


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