Skip to main content
Article
Timed Diels-Alder reactions
Journal of the American Chemical Society
  • George A. Kraus, Iowa State University
  • Michael J. Taschner, Iowa State University
Document Type
Article
Publication Version
Published Version
Publication Date
3-1-1980
DOI
10.1021/ja00526a036
Abstract

In this paper a unique approach to the synthesis of polycyclic ring systems is disclosed. The approach features an intermolecular Diels-Alder reaction followed by an intramolecular Diels-Alder reaction where the regiochemistry of addition is controlled by substituents on the bisdiene and bisdienophile. This methodology has been applied to the synthesis of the fluorenone ring system.

Comments

Reprinted (adapted) with permission from Journal of the American Chemical Society, 102(6); 1974-1977. Doi: 10.1021/ja00526a036. Copyright 1980 American Chemical Society.

Copyright Owner
American Chemical Society
Language
en
File Format
application/pdf
Citation Information
George A. Kraus and Michael J. Taschner. "Timed Diels-Alder reactions" Journal of the American Chemical Society Vol. 102 Iss. 6 (1980) p. 1974 - 1977
Available at: http://works.bepress.com/george_kraus/36/