Author: Ronald Neil Buckle
Publisher:
ISBN:
Category : Asymmetric synthesis
Languages : en
Pages : 0
Book Description
Asymmetric Diels-Alder Studies Involving Chiral Acetylenic Diesters and Investigations of an Intramolecular Diels-Alder Approach to the Pentalenolactones
Author: Ronald Neil Buckle
Publisher:
ISBN:
Category : Asymmetric synthesis
Languages : en
Pages : 0
Book Description
Publisher:
ISBN:
Category : Asymmetric synthesis
Languages : en
Pages : 0
Book Description
Asymmetric Diels-Alder Studies Involving Chiral Acetylenic Diesters and Investigations of an Intramolecular Diels-Alder Approach to the Pentalenolactones [microform]
Author: Ronald Neil Buckle
Publisher: National Library of Canada = Bibliothèque nationale du Canada
ISBN:
Category : Asymmetric synthesis
Languages : en
Pages : 640
Book Description
Publisher: National Library of Canada = Bibliothèque nationale du Canada
ISBN:
Category : Asymmetric synthesis
Languages : en
Pages : 640
Book Description
Dissertation Abstracts International
Author:
Publisher:
ISBN:
Category : Dissertations, Academic
Languages : en
Pages : 680
Book Description
Publisher:
ISBN:
Category : Dissertations, Academic
Languages : en
Pages : 680
Book Description
Intramolecular Diels-Alder and Alder Ene Reactions
Author: Douglass F. Taber
Publisher: Springer Science & Business Media
ISBN: 3642692338
Category : Science
Languages : en
Pages : 106
Book Description
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.
Publisher: Springer Science & Business Media
ISBN: 3642692338
Category : Science
Languages : en
Pages : 106
Book Description
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.
Part I: A Convergent Synthetic Scheme to Quassin
Author: Colleen Joan Northcott
Publisher:
ISBN:
Category : Diels-Alder reaction
Languages : en
Pages : 660
Book Description
Publisher:
ISBN:
Category : Diels-Alder reaction
Languages : en
Pages : 660
Book Description
The Intramolecular Diels Alder as a Stereospecific Approach to Ilicicolin H
Author: Isaac Byron Horton
Publisher:
ISBN:
Category : Diels-Alder reaction
Languages : en
Pages : 432
Book Description
Publisher:
ISBN:
Category : Diels-Alder reaction
Languages : en
Pages : 432
Book Description
American Doctoral Dissertations
Author:
Publisher:
ISBN:
Category : Dissertation abstracts
Languages : en
Pages : 784
Book Description
Publisher:
ISBN:
Category : Dissertation abstracts
Languages : en
Pages : 784
Book Description
Asymmetric Intramolecular Diels-Alder Reactions
Author: Amy Pia Essenfeld
Publisher:
ISBN:
Category :
Languages : en
Pages : 398
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 398
Book Description
Investigations Into the Scope of a Remote Stereocontrolled Asymmetric Intramolecular Diels-Alder Reaction
Author: Christian A. Clarke
Publisher:
ISBN:
Category : Asymmetric synthesis
Languages : en
Pages : 98
Book Description
Publisher:
ISBN:
Category : Asymmetric synthesis
Languages : en
Pages : 98
Book Description
Intramolecular Diels-Alder Reactions of Alkenylboranes & a Hetero Diels-Alder Approach to the Total Synthesis of Martinelline
Author: Denny Lin
Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description