This edition has been extensively revised and enlarged to take account of recent developments. It emphasises the basic principles of the subject which remain essentially unchanged. The first ten chapters lay the ground work for carbon-carbon bond formation, functional group transformations, etc. with detailed additions which reflect new work. The remaining chapters on boron, phosphorus and silicon reagents, and selected syntheses have undergone extensive revisions. Chapters on selenium reagents and asymmetric synethesis are completely new.
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"...an excellent guide both to reactions which are of importance in synthesis and to the principles underlying the formation of various types of bonds." (Endeavour)
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Inside This Book
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Key Phrases - Statistically Improbable Phrases (SIPs):
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electrophilic carbon species, tervalent phosphorus compounds, nucleophilic carbon species, related nucleophiles, correct disconnection, benzeneseleninic acid, allylic selenides, carbanion source, bimolecular reduction, new stereogenic centre, mixed condensations, benzeneseleninic anhydride, stabilized carbanions, anionic centre, other organometallic reagents, selenium reagents, functional group chemistry, phosphorus reagents, stereogenic centres, boron reagents, synthetic equivalents, electrocyclic ring closure, lithium aluminium hydride, dissolving metal reduction, reductive ring opening Key Phrases - Capitalized Phrases (CAPs): (learn more)
Reduction Table, Group Structure Abbreviation Normal, Functional Group Interconversion Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
electrophilic carbon species, tervalent phosphorus compounds, nucleophilic carbon species, related nucleophiles, correct disconnection, benzeneseleninic acid, allylic selenides, carbanion source, bimolecular reduction, new stereogenic centre, mixed condensations, benzeneseleninic anhydride, stabilized carbanions, anionic centre, other organometallic reagents, selenium reagents, functional group chemistry, phosphorus reagents, stereogenic centres, boron reagents, synthetic equivalents, electrocyclic ring closure, lithium aluminium hydride, dissolving metal reduction, reductive ring opening Key Phrases - Capitalized Phrases (CAPs): (learn more)
Reduction Table, Group Structure Abbreviation Normal, Functional Group Interconversion Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Citations (learn more)
3
books
cite this book:
- Strategies and Tactics in Organic Synthesis, Volume 3 by Thomas Lindberg on page 415
- Umpoled Synthons: A Survey of Sources and Uses in Synthesis by Tapio A. Hase in Back Matter
- An Introduction to Organosulfur Chemistry by R. J. Cremlyn on page 39
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