Enantioselective Total Synthesis and Structure Revision of Spirodihydrobenzofuranlactam 1. Total Synthesis of Stachybotrylactam
Author:
Affiliation:
1. Department of Chemistry, University of Rochester, Rochester, New York 14627
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol030039j
Reference17 articles.
1. Novel Spirodihydrobenzofuranlactams as Antagonists of Endothelin and as Inhibitors of HIV-1 Protease Produced by Stachybotrys sp. I. Fermentation, Isolation and Biological Activity.
2. Novel Spirodihydrobenzofuranlactams as Antagonists of Endothelin and as Inhibitors of HIV-1 Protease Produced by Stachybotrys sp. II. Structure Determination.
3. Buchschacher, P.; Fürst, A.; Gutzwiller, J.Organic Syntheses; Wiley: New York, 1990; Collect. Vol. VII, p 368.
4. Ring Formylation of Bromobenzoate Esters by Direct Metalation
5. An efficient approach to chiral, nonracemic trans-decahydro-5,8a-dimethyl-1,6-naphthalenedione derivatives. Total synthesis of (+)-pallescensin A
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