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 t...

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主要作者: Li, Jie Jack
格式: Livre numérique
語言:Anglais
出版: Berlin, Heidelberg : Springer Berlin Heidelberg 2006.
Cham : Springer Nature
版:Third Expanded Edition.
在線閱讀:Accès sur la plateforme de l'éditeur
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Edition sous un autre format:• Name reactions, a collection of detailed reaction mechanisms, Jie Jack Li, 3rd expanded ed., Berlin, Springer, 2006, 1 vol. (XX-652 p.), 3-540-30030-9
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505 1 |a Alder ene reaction Aldol condensation Algar-Flynn-Oyamada Reaction Allan-Robinson reaction Appel reaction Arndt-Eistert homologation Baeyer-Villiger oxidation Baker-Venkataraman rearrangement Bamberger rearrangement Bamford-Stevens reaction Barbier coupling reaction Bargellini reaction Bartoli indole synthesis Barton radical decarboxylation Barton-McCombie deoxygenation Barton nitrite photolysis Barton-Zard reaction Batcho-Leimgruber indole synthesis Baylis-Hillman reaction Beckmann rearrangement Beirut reaction Benzilic acid rearrangement Benzoin condensation Bergman cyclization Biginelli pyrimidone synthesis Birch reduction Bischler-Möhlau indole synthesis Bischler-Napieralski reaction Blaise reaction Blanc chloromethylation Blum aziridine synthesis Boekelheide reaction Boger pyridine synthesis Borch reductive amination Borsche-Drechsel cyclization Boulton-Katritzky rearrangement Bouveault aldehyde synthesis Bouveault-Blanc reduction Boyland-Sims oxidation Bradsher reaction Brook rearrangement Brown hydroboration Bucherer carbazole synthesis Bucherer reaction Bucherer-Bergs reaction Büchner-Curtius-Schlotterbeck reaction Büchner method of ring expansion Buchwald-Hartwig C-N and C-O bond formation reactions Burgess dehydrating reagent Cadiot-Chodkiewicz coupling Camps quinolinol synthesis 
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506 |a Conditions particulières de réutilisation pour les bénéficiaires des licences nationales. https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017 
520 |a 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. Some praise for the previous edition: "This is an excellent book for arrow pushing and learning organic name reactions as encountered in graduate school . . . Li s book contains reactions of all mechanistic classes . . . The book is nicely balanced, containing modern-day reactions for assembly of stereocomplex molecules. Reactions such as the Corey-Bakshi-Shibata reduction are analyzed. This book is a good reference text that fills a void that has existed for some time. It is both an excellent tool for learning and a good reference source." JOURNAL OF CHEMICAL EDUCATION 
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