Polyene Cyclization Promoted by the Cross-Conjugated α-Carbalkoxy Enone System. Observation on a Putative 1,5-Hydride/1,3-Alkyl Shift under Lewis Acid Catalysis-Reference-Cited by-同舟云学术

Polyene Cyclization Promoted by the Cross-Conjugated α-Carbalkoxy Enone System. Observation on a Putative 1,5-Hydride/1,3-Alkyl Shift under Lewis Acid Catalysis

Published:2007-12-04 Issue:1 Volume:10 Page:121-123
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chou Ho-Hsuan¹,Wu Huang-Min¹,Wu Jen-Dar¹,Ly Tai Wei¹,Jan Ning-Wei¹,Shia Kak-Shan¹,Liu Hsing-Jang¹

Affiliation:

1. Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan 30013, R.O.C., Actimis Pharmaceuticals, Inc., 10835 Road to the Cure, Suite 200, San Diego, California 92121, and Division of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Miaoli County 350, Taiwan, R.O.C.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol702631q

Reference24 articles.

1. Bartlett, P. A. inAsymmetric Synthesis; Morrison, J. D., Ed.; Academic Press: Orlando, 1984; Vol. 3, pp 341−409.

2. Biomimetic polyene cyclizations

3. Total synthesis of polycarbocyclic sesquiterpenes

4. Bioorganic chemistry. Total synthesis of tetra- and pentacyclic triterpenoids

5. Structural and stereochemical course of in vitro epoxy olefin cyclization. Diterpenoid intermediates

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