BEHAVIOR OF STEREOISOMERIC O-METHYLTYROSYL-P-NITROPHENYLALANINES WITHIN THE BETA-CYCLODEXTRIN CAVITY
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DOI
10.1039/c39950002437
Abstract
Cyclisation of the L,D- and L,L-O-methyltyrosyl-p-nitrophenylalanine methyl esters is studied; in the presence of beta-cyclodextrin, reaction took place only with the L,L-isomer.