Synthesis of the peptidic alpha-hydroxy amides phebestin, probestin, and bestatin from alpha-keto amide precursors

Citation
Hh. Wasserman et al., Synthesis of the peptidic alpha-hydroxy amides phebestin, probestin, and bestatin from alpha-keto amide precursors, TETRAHEDR L, 40(34), 1999, pp. 6163-6166
Citations number
23
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
34
Year of publication
1999
Pages
6163 - 6166
Database
ISI
SICI code
0040-4039(19990820)40:34<6163:SOTPAA>2.0.ZU;2-Z
Abstract
Aminopeptidase inhibitors, phebestin, probestin and bestatin have been prep ared by stereospecific reduction of alpha-keto amide precursors using zinc borohydride. (C) 1999 Elsevier Science Ltd. All rights reserved.