The discovery of catalytically active peptides through combinatorial chemistry.

Abstract:

:In recent years, ogliopeptides have enjoyed ever increasing interest in two areas: first, approaches to biomimetic enzyme-like activity; and second, as metal-free catalysts for enantioselective transformations of synthetic interest. The discovery and optimization of peptides for these purposes has often used the methodology of combinatorial chemistry. Examples include the screening of peptide libraries for ester and phosphate cleavage, aided by novel chromogenic and gel-based assays, and optimization of metal-free peptide catalysts for asymmetric epoxidation, enantioselective acylation/phosphorylation, conjugate addition to enimides, and hydrocyanation of imines (Strecker-reaction).

journal_name

Curr Opin Chem Biol

authors

Berkessel A

doi

10.1016/s1367-5931(03)00065-6

subject

Has Abstract

pub_date

2003-06-01 00:00:00

pages

409-19

issue

3

eissn

1367-5931

issn

1879-0402

pii

S1367593103000656

journal_volume

7

pub_type

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