Mechanism of enantioselective ester cleavage by histidine-containing peptides at a micellar interface. 2. Effect of changing peptide chain length

DOI: 10.1002/recl.19921111101

Source and publish data:

Recueil des Travaux Chimiques des Pays-Bas p. 459 - 468 (1992)

Update date:2022-08-04

Topics: Chiral Enantioselective Hydrolysis Ester Cleavage Catalysis Spectroscopy

Authors:

Cleij, Marco C.

Drenth, Wiendelt

Nolte, Roeland J. M.

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Article abstract of DOI:10.1002/recl.19921111101

Chiral p-nitrophenyl esters derived from the amino acid phenylalanine are cleaved by various histidine-containing tripeptides and higher oligopeptides as catalysts at a micellar interface.It is assumed that the oligopeptides adopt an internally hydrogen-b

Full text of DOI:10.1002/recl.19921111101

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