The Synthesis of an Exhaustively Stereodiversified Library of cis-1,5 Enediols by Silyl-Tethered Ring-Closing Metathesis
Author:
Affiliation:
1. Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0159569
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1. Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery
2. Stereochemistry as a Diversity Element: Solid-Phase Synthesis of Cyclic RGD Peptide Derivatives by Asymmetric Catalysis
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4. A Modular Synthetic Approach toward Exhaustively Stereodiversified Ligand Libraries
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