Organic Syntheses Based on Name Reactions

A Practical Guide to Over 800 Transformations

Alfred Hassner,Irishi Namboothiri

• Publisher: Elsevier
• Year: 2011
• ISBN:
  9780080966311
• Edition: 3
• Topic: Scienze fisiche
• Subtopic: Chimica organica

Organic Syntheses Based on Named Reactions is an indispensable reference companion for chemistry students and researchers. Building on Hassner & Stumer's highly regarded 2e, this new work reviews 750 reactions, with over 100 new stereoselective and regioselective reactions. Each A-Z entry provides a carefully condensed summary of valuable information that a chemist needs to understand and utilize these fundamental reactions in their work, including brief practical details. The book is illustrated with real synthetic examples from the literature and about 3, 400 references to the primary literature to aid further reading. Extensive indexes (name, reagent, reaction) and a very useful functional group transformation index help the reader fully navigate this extensive collection of important reactions. With its comprehensive coverage, superb organization and quality of presentation, this long-awaited new edition belongs on the shelf of every organic chemist.

• Handy reference guide that explains 750 established named processes and methods that are trusted and used by organic chemists to synthesize or transform molecules
• Provides key data on each transformation including background, mechanism and--uniquely to books in this area--experimental details
• Extensive and multiple indexes allow the reader to search for information as and how they want and to rapidly plan transformations

Table of contents

• Cover image
• Table of Contents
• Front matter
• Copyright
• Foreword by D. Seebach
• Foreword by S. Danishefsky
• Preface to the Third Edition
• Preface to the Second Edition
• Preface to the First Edition
• An Overview of Synthesis Related Name Reactions
• Overview - Pd Catalyzed C–C Coupling Name Reactions
• List of Abbreviations
• ABIKO–MASAMUNE Asymmetric Aldol Reaction to AUWERS–INHOFFEN Dienone-Phenol Rearrangement
• BAER–FISCHER Amino Sugar Synthesis to BURTON Aromatic Trifluoromethylation
• CADOGAN Nitroaromatics Cyclization to CURTIUS Acyl Azide Rearrangement
• DAKIN Phenol Oxidation to DUTT–WORMALL Azide Synthesis
• EATON Acid Reagent to EVANS Chiral Auxiliary
• FAVORSKI α-Haloketone Rearrangement to FŰRSTNER Fe Catalyzed CC Coupling
• GABRIEL–HEINE Aziridine Isomerization to GUY–LEMAIRE–GUETTE Halogenation Reagent
• HADDADIN–ISSIDORIDES Quinoxaline Synthesis to HUNSDIECKER Halodecarboxylation
• IRELAND Allyl Ester Rearrangement to IVANOV Carboxy-Grignard Reagent
• JACOBSEN Asymmetric Epoxidation to JUNG–OLAH–VORONKOV Ether Cleavage
• KABACHNIK–FIELD Aminophosphonate Synthesis to KURSANOV–PARNES Ionic Hydrogenation
• LADENBURG Pyridine Benzylation to LUCHE Zn Allylation
• MACDONALD Porphyrin Synthesis to MYERS–SAITO Cycloaromatization
• NAGATA Aluminium Cyanide Reagent to NUGENT–RAJANBABU Epoxide Homolysis
• O'DONNELL Amino Acid Synthesis to Oxy-COPE Hydroxydiene Rearrangement
• PAAL–KNORR Pyrrole Synthesis to PURDIE Sugar OH Methylation
• RAMBERG–BACKLUND Olefin Synthesis to RUZICKA–FUKUSHIMA Ketosteroid Rearrangement
• SAEGUSA Enone Synthesis to SZARVASY–SCHÖPF Carbomethoxylation
• TAKAI Zn CO Olefination to TSUJI–TROST Allylation
• UEMURA–DOYLE Rh Allylic Oxidation to URECH Cyanohydrin Synthesis
• VAN BOOM Phosphorylating Reagent to VORBRÜGGEN Nucleoside Synthesis
• WACKER–TSUJI Olefin Oxidation to WÜRTZ Coupling
• YAMADA Peptide Coupling to YONEMITSU 3-Component Condensation
• ZARD Radical Aminomethylation via Xanthates to ZVILICHOVSKY Heterocycle Synthesis
• Names Index
• Reagents Index
• Reactions Index
• Functional Group Transformation Index