THE ENANTIOSPECIFIC SYNTHESIS OF NOVEL LYSINE ANALOGS INCORPORATING APYRROLIDINE CONTAINING SIDE-CHAIN

Authors
MURRAY PJ STARKEY ID DAVIES JE
Citation
Pj. Murray et al., THE ENANTIOSPECIFIC SYNTHESIS OF NOVEL LYSINE ANALOGS INCORPORATING APYRROLIDINE CONTAINING SIDE-CHAIN, Tetrahedron letters, 39(37), 1998, pp. 6721-6724
Citations number
6
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
39
Issue
37
Year of publication
1998
Pages
6721 - 6724
Database
ISI
SICI code
0040-4039(1998)39:37<6721:TESONL>2.0.ZU;2-7
Abstract
Two novel analogues of lysine have been prepared in high enantiomeric and diastereomeric purity. These unnatural alpha-amino acids possess m odified aminoalkyl side chains incorporating a pyrrolidine nucleus as a cyclic constraint. (C) 1998 Elsevier Science Ltd. AII rights reserve d.