A crosslinked, L-histidyl group-introduced polymer catalyst, which was imprinted by a transition-state analogue of phenyl 1-benzyloxycarbonylamino-3-methylpentylphosphonate in the hydrolysis of pnitrophenyl N-carbobenzoxy-L-leucinate, was prepared from poly(2-methyl-2-oxazoline). The catalyst enhanced the hydrolysis of the L-leucine ester, in comparison to the hydrolysis of the L-phenylalanine and L-alanine esters
Посилання на статтю:
Preparation and catalytic property of L-histidyl group-introduced, crosslinked poly(ethylene imine)s imprinted by a transition-state analogue of an esterolysis reaction / Katsutoshi Ohkubo and Yasuo Urata, Yuhji Honda and Yasuhiro Nakashima // Polymer. – 1994. – Vol 35. – P. 5372-5374.