Intramolecular Diels-Alder and Alder Ene Reactions

Author:   Douglass F. Taber
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Edition:   Softcover reprint of the original 1st ed. 1984
Volume:   18
ISBN:  

9783642692352


Pages:   97
Publication Date:   06 December 2011
Format:   Paperback
Availability:   Manufactured on demand   Availability explained
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Intramolecular Diels-Alder and Alder Ene Reactions


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Overview

The Diels-Alder reaction has long been a powerful tool in organic synthesis. In recent years, the Alder ene reaction has also achieved some prominence. From the beginning, it was apparent that the intramolecular variants of these reactions would be feasible. Many such have been reported, but the results are widely scattered in the chemical literature. This volume is an attempt to synthesize results observed to date, and to suggest directions for future development. One of the limiting factors in the application of the intramolecular Diels­ Alder reaction has been the development of methods for the preparation of the requisite trienes. The fIrst chapter of this volume summarizes methods for the preparation of dienes and dienophiles. Examples representative of every general approach to 1,3-dienes and to dienophilic functional group combinations have been included. There are two questions one might ask in considering the prospective cyclization of a given triene: what are the factors that govern the rate of cyclization? and, for cyclizations that lead to the creation of one or more new chiral centers, what are the factors that govern diastereoselectivity? These questions are addressed in Chapter Two. The third chapter is devoted to the all-carbon intramolecular Alder ene reaction. The tables in that chapter summarize all examples that could be found in the literature through 1981, with several additional examples from 1982. Leading references to heterocyclic ene reactions are also included in this chapter.

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Author:   Douglass F. Taber
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Imprint:   Springer-Verlag Berlin and Heidelberg GmbH & Co. K
Edition:   Softcover reprint of the original 1st ed. 1984
Volume:   18
Dimensions:   Width: 17.00cm , Height: 0.60cm , Length: 24.40cm
Weight:   0.209kg
ISBN:  

9783642692352


ISBN 10:   3642692354
Pages:   97
Publication Date:   06 December 2011
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

Table of Contents

1. The Intramolecular Diels-Alder Reaction: Variations and Scope.- I. Introduction.- II. Range and Preparation of Dienes.- III. Range and Preparation of Dienophiles.- IV. Heterodienes and Dienophiles.- V. Catalysis of the Reaction.- VI. Conclusion.- VII. References.- 2. The Intramolecular Diels-Alder Reaction: Reactivity and Stereocontrol.- I. Introduction.- II. Factors Influencing the Rate of Cyclization.- III. Factors Influencing the Stereochemical Outcome of the Cyclization.- IV. Summary.- V. References.- 3. The Intramolecular Alder Ene Reaction.- I. Introduction.- II. Reactivity of Ene Acceptors.- III. Reactivity of Ene Donors.- IV. Steric and Stereoelectronic Control Elements in the Intramolecular Ene Reaction.- V. Directions for the Future.- VI. Tables.- VII. References.

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