Skip to main content
Article
Diels−Alder Reactions of Quinol Lactones:  A Change of Regioselectivity with Stannic Chloride Catalysis
The Journal of Organic Chemistry
  • George A. Kraus, Iowa State University
  • Wenge Cui, Iowa State University
Document Type
Article
Publication Version
Published Version
Publication Date
12-5-2002
DOI
10.1021/jo020366p
Abstract
Lewis acid-mediated Diels−Alder reactions of quinol lactone 2 gave regioselectivity opposite to that of the uncatalyzed reaction. Compound 12 is proposed as the reactive intermediate generated by the reaction of 2 with stannic chloride.
Comments

Reprinted (adapted) with permission from The Journal of Organic Chemistry; 67(26); 9475-9476. Doi: 10.1021/jo020366p. Copyright 2002 American Chemical Society.

Copyright Owner
American Chemical Society
Language
en
File Format
application/pdf
Citation Information
George A. Kraus and Wenge Cui. "Diels−Alder Reactions of Quinol Lactones:  A Change of Regioselectivity with Stannic Chloride Catalysis" The Journal of Organic Chemistry Vol. 67 Iss. 26 (2002) p. 9475 - 9476
Available at: http://works.bepress.com/george_kraus/137/