ENANTIOSELECTIVE RECOGNITION OF HISTIDINE AND LYSINE ESTERS BY PORPHYRIN CHIRAL CLEFTS AND DETECTION OF AMINO-ACID CONFORMATIONS IN THE BOUND-STATE

Citation
Mj. Crossley et al., ENANTIOSELECTIVE RECOGNITION OF HISTIDINE AND LYSINE ESTERS BY PORPHYRIN CHIRAL CLEFTS AND DETECTION OF AMINO-ACID CONFORMATIONS IN THE BOUND-STATE, Journal of the Chemical Society, Chemical Communications, (18), 1995, pp. 1925-1927
Citations number
8
Categorie Soggetti
Chemistry
ISSN journal
00224936
Issue
18
Year of publication
1995
Pages
1925 - 1927
Database
ISI
SICI code
0022-4936(1995):18<1925:EROHAL>2.0.ZU;2-9
Abstract
Resolution of the bisporphyrin Troger's base analogue 1 affords homoch iral clefts that tightly bind histidine esters in 80-86% e.e. and lysi ne benzyl ester in 48% e.e.; the histidine esters are bound in fixed c onformations that can be readily detected by H-1 NMR spectroscopy as a result of the large dispersion of proton resonances by the ring curre nts of the two porphyrins.