DIASTEREOSELECTIVE SYNTHESIS OF THE KEY LACTONE INTERMEDIATE FOR THE PREPARATION OF HYDROXYETHYLENE DIPEPTIDE ISOSTERES

Authors
LAGU BR LIOTTA DC
Citation
Br. Lagu et Dc. Liotta, DIASTEREOSELECTIVE SYNTHESIS OF THE KEY LACTONE INTERMEDIATE FOR THE PREPARATION OF HYDROXYETHYLENE DIPEPTIDE ISOSTERES, Tetrahedron letters, 35(4), 1994, pp. 547-550
Citations number
16
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
4
Year of publication
1994
Pages
547 - 550
Database
ISI
SICI code
0040-4039(1994)35:4<547:DSOTKL>2.0.ZU;2-J
Abstract
An efficient and highly stereoselective route for preparing hydroxyeth ylene dipeptide isosteres from alpha-N,N-dibenzylamino ketones has bee n developed.