
Stereoselectivity in Organic Synthesis
Garry Procter(Author)
Oxford University Press
Published on 23. April 1998
Book
Paperback/Softback
96 pages
978-0-19-855957-3 (ISBN)
Description
This clear and concise text is concerned with the reactions used in stereoselective organic synthesis. It sets out to consider the general principles upon which such reactions are founded, especially stereoelectronic effects, and how these are applied to a wide range of stereospecific and stereoselective organic reactions used in organic synthesis today. The general topics covered include: reactions of carbonyl compounds, aldol reactions, additions to C-C double bonds, oxidation and reduction, rearrangements, and enzyme catalysed hydrolysis. Reactions whose stereoselectivity is either substrate controlled, reagent controlled or controlled by a catalyst are covered, and where appropriate, examples of their application in organic synthesis are provided. Fully illustrated throughout, with set problems and suggestions for further reading to accompany each chapter, this informative text will be an invaluable study aid for all undergraduate chemistry students. Undergraduates in related subjects studying chemistry to second year level or higher will also find this book useful.
More details
Series
Language
English
Place of publication
Oxford
United Kingdom
Target group
College/higher education
Illustrations
numerous line figures
Dimensions
Height: 245 mm
Width: 190 mm
Thickness: 6 mm
Weight
208 gr
ISBN-13
978-0-19-855957-3 (9780198559573)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Person
Professor Garry Procter, Professor of Organic Chemistry, Department of Chemistry and Applied Chemistry, University of Salford
Author
Professor of Organic ChemistryProfessor of Organic Chemistry, University of Salford
Content
1. Introduction ; 2. Stereochemistry of reactions ; 3. Additions to carbonyl compounds ; 4. Reactions of enolates ; 5. Aldol reactions ; 6. Additions to double bonds ; 7. Reduction ; 8. Oxidation ; 9. Rearrangements ; 10. Hydrolysis and esterification ; Answers to problems ; Index