Research and Development of an Efficient Synthesis of Hexahydrofuro[2,3-b]furan-3-ol Moiety—A Key Component of the HIV Protease Inhibitor Candidates
Author:
Affiliation:
1. Process Research Department, Gilead Sciences, Inc., Foster City, California 94404
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/op700160a
Reference46 articles.
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2. Clerodane diterpenoids
3. Total synthesis of (.+-.)-asteltoxin
4. Stereoselective synthesis of the bis(tetrahydrofuran) moiety (C-1 to C-9) of (+)-asteltoxin, a novel mycotoxin from aspergillus stellatus
5. Clerodane and aromatic seco-clerodane diterpenoids from salvia rhyacophua.
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