Acylnitrene Route to Vicinal Amino Alcohols. Application to the Synthesis of (−)-Bestatin and Analogues
Author:
Affiliation:
1. Division of Medicinal Chemistry, College of Pharmacy, and the Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio 43210
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9823893
Reference23 articles.
1. Bestatin, an inhibitor of aminopeptidase B, produced by actinomycetes.
2. Isolation and Synthesis of Novel Farnesyl Protein Transferase Inhibitors, Valinoctins A and B, from Streptomyces Strain MJ858-NF3
3. Microginin, an angiotensin-converting enzyme inhibitor from the blue-green alga Microcystis aeruginosa
4. Enhancement of delayed-type hypersensitivity by bestatin, an inhibitor of aminopeptidase B and leucine aminopeptidase.
5. Synthesis of Vicinal Amino Alcohols via a Tandem Acylnitrene Aziridination−Aziridine Ring Opening
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