A new stereoselective approach to beta-hydroxy-alpha-aminoacids and dipeptides

Authors
Di Felice, P Porzi, G Sandri, S
Citation
P. Di Felice et al., A new stereoselective approach to beta-hydroxy-alpha-aminoacids and dipeptides, TETRAHEDR-A, 10(11), 1999, pp. 2191-2201
Citations number
14
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
10
Issue
11
Year of publication
1999
Pages
2191 - 2201
Database
ISI
SICI code
0957-4166(19990604)10:11<2191:ANSATB>2.0.ZU;2-8
Abstract
The chiral synthons 1, 2 and 1' were submitted to aldol condensation to ach ieve both beta-hydroxy-alpha-aminoacids and dipeptides. The configuration o f the new stereogenic centers was assigned on the basis of H-1 NMR spectros copic data. (C) 1999 Elsevier Science Ltd. All rights reserved.