Lewis Acids and Selectivity in Organic Synthesis

Author:   M. Santelli ,  J.-M. Pons
Publisher:   Taylor & Francis Inc
Volume:   2
ISBN:  

9780849378669


Pages:   352
Publication Date:   21 November 1995
Format:   Hardback
Availability:   Out of stock   Availability explained


Our Price $654.59 Quantity:  
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Lewis Acids and Selectivity in Organic Synthesis


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Overview

Lewis acids provide inexpensive access to elaborated molecules obtained with high selectivities (regio-, stereo-, and enantioselectivity). Lewis Acids and Selectivity in Organic Synthesis is the first book to deal with these new and promising roles of Lewis acids. The book begins with general considerations on Lewis acids and a description of Lewis acid-carbonyl complexes, which are involved in most of the reactions described: ene reactions, allylsilane and allyltin addition to carbonyl compounds, addition of nucleophiles to acetals, conjugated addition of allylsilanes and allyltins to unsaturated carbonyl compounds (Sakurai reaction), and Diels-Alder reaction. Subsequent chapters examine these issue in detail, with special attention given to the way Lewis acids induce diastereo- and enantioselectivity. The extensive use of schemes (approximately 1000) ensures rapid visual uptake of the information. Lewis Acids and Selectivity in Organic Synthesis serves as a valuable source of information for all who face the challenge of selectivity in organic synthesis.

Full Product Details

Author:   M. Santelli ,  J.-M. Pons
Publisher:   Taylor & Francis Inc
Imprint:   CRC Press Inc
Volume:   2
Dimensions:   Width: 15.60cm , Height: 2.50cm , Length: 23.40cm
Weight:   0.688kg
ISBN:  

9780849378669


ISBN 10:   0849378664
Pages:   352
Publication Date:   21 November 1995
Audience:   College/higher education ,  Professional and scholarly ,  Postgraduate, Research & Scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Out of Print
Availability:   Out of stock   Availability explained

Table of Contents

Lewis Acids and Their Complexes with Lewis Bases Lewis Acid-Promoted Ene Reaction Lewis Acid-Promoted Allylsilanes and Allylstannanes Addition to Aldehydes and Ketones Lewis Acid-Promoted Acetal Substitution Reactions Sakurai Reaction: Lewis Acid-Promoted Allylsilanes and Allylstannanes 1,4-Addition to Unsaturated Ketones Lewis Acid-Promoted Diels-Alder Reaction Index

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Santelli\, M.; Pons\, J.-M.

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