THE SYNTHESIS AND CONFORMATIONAL-ANALYSIS OF A PAIR OF DIASTEREOMERIC, CONFORMATIONALLY CONSTRAINED PEPTIDES WITH OPPOSITE AMIDE BOND GEOMETRIES

Authors
CUMBERBATCH S NORTH M ZAGOTTO G
Citation
S. Cumberbatch et al., THE SYNTHESIS AND CONFORMATIONAL-ANALYSIS OF A PAIR OF DIASTEREOMERIC, CONFORMATIONALLY CONSTRAINED PEPTIDES WITH OPPOSITE AMIDE BOND GEOMETRIES, Tetrahedron, 49(40), 1993, pp. 9049-9066
Citations number
26
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
49
Issue
40
Year of publication
1993
Pages
9049 - 9066
Database
ISI
SICI code
0040-4020(1993)49:40<9049:TSACOA>2.0.ZU;2-5
Abstract
Eight membered ring containing, conformationally constrained peptides derived from cyclo-[(R)-cysteinyl-(R)-penicillamine] contain a cis ami de bond, whilst the diastereomeric peptides derived from cyclo-[(R)-cy steinyl-(S)-penicillamine] contain a trans amide bond.