Synthesis of the peptidic α-hydroxy amides phebestin, probestin, and bestatin from α-keto amide precursors
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Phebestin, a New Inhibitor of Aminopeptidase N, Produced by Streptomyces sp. MJ716-m3.
2. Probestin, a new inhibitor of aminopeptidase M, produced by Streptomyces azureus MH663-2F6. I. Taxonomy, production, isolation, physico-chemical properties and biological activities.
3. Probestin, a new inhibitor of aminopeptidase M, produced by Streptomyces azureus MH663-2F6. II. Structure determination of probestin.
4. Bestatin, an inhibitor of aminopeptidase B, produced by actinomycetes.
5. The structure of bestatin.
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1. Asymmetric Transfer Hydrogenation of α-Keto Amides; Highly Enantioselective Formation of Malic Acid Diamides and α-Hydroxyamides;Organic Letters;2021-09-29
2. Facile Synthesis of Internal and C-Terminal Peptide α -Ketoamides with Fmoc-Solid Phase Peptide Synthesis;Helvetica Chimica Acta;2018-05
3. Highly enantioselective Ir/f-amphox-catalyzed hydrogenation of ketoamides: efficient access to chiral hydroxy amides;Organic Chemistry Frontiers;2018
4. Anchimeric‐Assisted Spontaneous Hydrolysis of Cyanohydrins Under Ambient Conditions: Implications for Cyanide‐Initiated Selective Transformations;Chemistry – A European Journal;2017-06-13
5. Recent Developments in General Methodologies for the Synthesis of α-Ketoamides;Chemical Reviews;2016-02-16
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