This book covers over 320 classical as well as contemporary name reactions. Each reaction is delineated by its detailed step-by-step, electron-pushing mechanism and supplemented with references. This fifth edition adds 27 new name reactions.
In this fifth edition of Jack Jie Li's seminal "Name Reactions", the author has added twenty-seven new name reactions to reflect the recent advances in organic chemistry. As in previous editions, each reaction is delineated by its detailed step-by-step, electron-pushing mechanism and supplemented with the original and the latest references, especially from review articles. Now with addition of many synthetic applications, this book is not only an indispensable resource for advanced undergraduate and graduate students, but is also a good reference book for all organic chemists in both industry and academia.
Unlike other books on name reactions in organic chemistry, Name Reactions, A Collection of Detailed Reaction Mechanisms and Synthetic Applications focuses on the reaction mechanisms. It covers over 320 classical as well as contemporary name reactions.
Inhaltsverzeichnis
From the content:Alder ene reaction.-Aldol condensation.-Algar Flynn Oyamada reaction.-Allan Robinson reaction.-Arndt Eistert homologation.-Baeyer Villiger oxidation.-Baker Venkataraman rearrangement.-Bamford Stevens reaction.-Baran reagents.-Barbier 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.-Abnormal Beckmann rearrangement.-Beirut reaction.-Benzilic acid rearrangement.-Benzoin condensation.-Bergman cyclization.-Biginelli reaction.-Birch reduction.-Bischler Möhlau indole synthesis.-Bischler Napieralski reaction.-Blaise reaction.-Blum Ittah aziridine synthesis.-Boekelheide reaction.-Boger pyridine synthesis.-Borch reductive amination.-Borsche Drechsel cyclization.-Boulton Katritzky rearrangement.-Bouveault aldehyde synthesis.-Bouveault Blanc reduction.
