Development of 5-(aminomethyl)pyrrole-2-carboxylic acid as a constrained surrogate of Gly-ΔAla and its application in peptidomimetic studies

Chakraborty, Tushar K. ; Krishna Mohan, B. ; Kiran Kumar, S. ; Kunwar, Ajit C. (2002) Development of 5-(aminomethyl)pyrrole-2-carboxylic acid as a constrained surrogate of Gly-ΔAla and its application in peptidomimetic studies Tetrahedron Letters, 43 (14). pp. 2589-2592. ISSN 0040-4039

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...

Related URL: http://dx.doi.org/10.1016/S0040-4039(02)00342-8

Abstract

A new peptidomimetic scaffold based on 5-(aminomethyl)pyrrole-2-carboxylic acid (1) is developed for the first time and used as a conformationally constrained surrogate of the Gly-ΔAla dipeptide isostere (2) to prepare peptides 3 and 4.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Peptide Mimetics; Dehydro Amino Acids; Hydrogen Bonding; Conformation; NMR
ID Code:20598
Deposited On:20 Nov 2010 13:54
Last Modified:22 May 2011 15:15

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