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
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.