Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4568
Title: Small ring constrained peptidomimetics. Synthesis of epoxy peptidomimetics, inhibitors of cysteine proteases
Authors: M., Demarcus
M. L., Ganadu
G. M., Mura
A., Porcheddu
L., Quaranta
G., Reginato
Taddei, Maurizio 
Issue Date: 2001
Project: None 
Journal: JOURNAL OF ORGANIC CHEMISTRY
Abstract: 
Different dipeptide analogues containing an oxirane ring in the place of the peptidic bond were prepared starting from naturally occurring amino acids. N-Fmoc-amino aldehydes were transformed into the corresponding methoxyvinyl derivatives through a Wittig reaction, and the addition of PhSeCl gave a series of different alpha -phenylselenyl aldehydes. Mukajiama reaction with silylketene acetals gave an intermediate product that was finally transformed into the desired oxiranyl peptidomimetics. Following this strategy we were able to control three new contiguous stereocenters starting from the enantiomerically pure amino acid. The dipeptide analogues could be used in SPPS on a SASRIN resin as the final epoxides were relatively unstable under acidic conditions. Moreover the synthesis of the single dipeptide mimetics was carried out on solid phase to generate a small library of epoxy peptidomimetics. Some of the products prepared in this work resulted as time-dependent reversible inhibitors of cysteine protease.
Description: 
45990
URI: http://hdl.handle.net/20.500.12779/4568
ISSN: 0022-3263
DOI: 10.1021/jo000961w
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