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Article
Regioselective Diels-Alder reactions. A synthesis of the left-hand portion of CC-1065
The Journal of Organic Chemistry
  • George A. Kraus, Iowa State University
  • Stephen Yue, Iowa State University
  • James Sy, Iowa State University
Document Type
Article
Publication Version
Published Version
Publication Date
1-1-1985
DOI
10.1021/jo00202a029
Abstract
Diene 2b reacted regioselectively with dienophiles. Adduct 6 was converted into the left-hand portion of CC-1065 in 10% overall yield.
Comments

Reprinted (adapted) with permission from The Journal of Organic Chemistry, 50(2); 283-284. Doi:10.1021/jo00202a029. Copyright 1985 American Chemical Society.

Copyright Owner
American Chemical Society
Language
en
File Format
application/pdf
Citation Information
George A. Kraus, Stephen Yue and James Sy. "Regioselective Diels-Alder reactions. A synthesis of the left-hand portion of CC-1065" The Journal of Organic Chemistry Vol. 50 Iss. 2 (1985) p. 283 - 284
Available at: http://works.bepress.com/george_kraus/176/