Moree, W.J., van der Marel, G.A. and Liskamp, R.M.J. (1991) Peptides containing a sulfinamide or a sulfonamide moiety: new transition-state analogues. Tetrahedron Letters, 32(3), pp. 409-412. (doi: 10.1016/S0040-4039(00)92641-8)
Full text not currently available from Enlighten.
Publisher's URL: http://dx.doi.org/10.1016/S0040-4039(00)92641-8
Abstract
A versatile synthesis of two new types of transition-state analogues of the amide bond hydrolysis is described: the sulfinamide and the sulfonamide moiety. These transition-state analogues are part of peptides which will be used for the generation of catalytic antibodies as well as for development of protease inhibitors.
Item Type: | Articles |
---|---|
Status: | Published |
Refereed: | Yes |
Glasgow Author(s) Enlighten ID: | Liskamp, Professor Robert |
Authors: | Moree, W.J., van der Marel, G.A., and Liskamp, R.M.J. |
College/School: | College of Science and Engineering > School of Chemistry |
Journal Name: | Tetrahedron Letters |
ISSN: | 0040-4039 |
University Staff: Request a correction | Enlighten Editors: Update this record