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Synthetic and Stereochemical Aspects
1st Edition, Volume 2 - October 17, 1997
Editor: Philip Page
Language: English
eBook ISBN:9780080538204
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The impact of organosulfur chemistry, especially in the areas of heterocyclic chemistry, stereocontrolled processes, and asymmetric synthesis, has led to a resurgence of interest…Read more
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The impact of organosulfur chemistry, especially in the areas of heterocyclic chemistry, stereocontrolled processes, and asymmetric synthesis, has led to a resurgence of interest in the field. This book is the secondin a series intended to provide coverage of topics of current interest throughout the whole range of organosulfur chemistry. Each volume is comprised of five or six chapters, each consisting of an in-depth, self-contained review in a well-defined area. This volume and its predecessor Organosulfur Chemistry, Synthetic Aspects will prove valuable references for researchers and practitioners in organic chemistry.
Methods of asymmetric sulfur oxidation processes
Preparation of chiral sulfoxides in nucleophilic displacement at sulfur
Conformational preferences of the sulfinyl group
Preparation and chemistry of unsaturated sulfoxides
Applications of sulfoxides as stereocontrol elements
The chemistry of sulfolenes
Organic chemists in research and industry.
H.B. Kagan and P. Diter, Asymmetric Sulfoxidation--Chemical and Enzymatic. S.M. Allin and P.C. Bulman Page, The Synthesis of Chiral Sulfoxides through Nucleophilic Displacement at Sulfur. E. Juaristi and M. Ordonez, Conformational Preference of the Sulfinyl Group in Six-Membered Heterocycles. S.M. Allin, S.J. Shuttleworth, and P.C. Bulman Page, Applications of Chiral Sulfoxides as Stereocontrol Elements in Organic Synthesis. J. Leonard, A.B Hague, andJ.A. Knight, Preparation of Substituted 3-Sulfolenes and Their Use as Precursors for Diels-Alder Dienes. Subject Index. Author Index.
No. of pages: 309
Language: English
Edition: 1
Volume: 2
Published: October 17, 1997
Imprint: Academic Press
eBook ISBN: 9780080538204
PP
Philip Page
Affiliations and expertise
Loughborough University, Dept. of Chemistry
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