Toward the Synthesis of Didemnaketal B: A Convergent Synthesis of the C9−C28 Subunit
Author:
Affiliation:
1. School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol801395q
Reference23 articles.
1. Didemnaketals A and B, HIV-1 protease inhibitors from the ascidian Didemnum sp
2. Relative and Absolute Stereochemistry of the Didemnaketals, Metabolites of a Palauan Ascidian, Didemnum sp.
3. Inhibition of HIV-1 Protease by a Subunit of Didemnaketal A
4. Synthetic studies of the HIV-1 protease inhibitive didemnaketals: stereocontrolled synthesis of an ester side chain
5. Synthetic studies of the HIV-1 protease inhibitive didemnaketals: precise and stereocontrolled synthesis of the key mother spiroketal
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