A Diosphenol-Based Strategy for the Total Synthesis of (−)-Terpestacin
Author:
Affiliation:
1. Department of Chemistry, Stanford University, Stanford, California 94305-5080
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja070571s
Reference13 articles.
1. Terpestacin, a new syncytium formation inhibitor from Arthrinium sp.
2. The First Total Synthesis of (±)-Terpestacin, HIV Syncytium Formation Inhibitor
3. The First Total Synthesis of Natural (+)-Terpestacin, Syncytium Formation Inhibitor.
4. Enantioselective Synthesis of (−)-Terpestacin and (−)-Fusaproliferin: Clarification of Optical Rotational Measurements and Absolute Configurational Assignments Establishes a Homochiral Structural Series
5. Synthesis of (−)-Terpestacin via Catalytic, Stereoselective Fragment Coupling: Siccanol Is Terpestacin, Not 11-epi-Terpestacin
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