A Ring Contraction Strategy toward a Diastereoselective Total Synthesis of (+)-Bakkenolide A
Author:
Affiliation:
1. Instituto de Química, Universidade de São Paulo, Av. Prof. Lineu Prestes, 748, CP 26077, CEP 05513-970 São Paulo SP, Brazil
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo100108b
Reference73 articles.
1. The structure of bakkenolide-A
2. Bakkenolide-A. Its distribution in Petasites species and cytotoxic properties
3. Syntheses of steroids having a bakkenolide-type spirolactone ring. I. Synthesis of 4'-methylenedihydrospiro-(5.ALPHA.-cholestane-3,3'(2'H)-furan)-2'-one.
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