Hjelmgaard, Thomas, Faure, Sophie, Caumes, Cécile, De Santis, Emiliana, Edwards, Alison A., Taillefumier, Claude (2009) Convenient Solution-Phase Synthesis and Conformational Studies of Novel Linear and Cyclic a,ß-Alternating Peptoids. Organic Letters, 11 (18). pp. 4100-4103. ISSN 1523-7052. (doi:10.1021/ol9015767) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:40411)
The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided. | |
Official URL: http://dx.doi.org/10.1021/ol9015767 |
Abstract
The synthesis of a novel family of peptidomimetics composed of linear and cyclic ?,?-alternating peptoids is described. Oligomers consisting of up to six peptoid residues (n = 1?3) were synthesized on large scale with use of an efficient iterative solution-phase method and longer oligomers (n = 4, 5) were obtained by the coupling of appropriately protected shorter oligomers. Preliminary conformational studies of these hybrid peptoids are reported.
Item Type: | Article |
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DOI/Identification number: | 10.1021/ol9015767 |
Additional information: | number of additional authors: 4; |
Subjects: | R Medicine > RS Pharmacy and materia medica |
Divisions: | Divisions > Division of Natural Sciences > Medway School of Pharmacy |
Depositing User: | Stewart Brownrigg |
Date Deposited: | 07 Mar 2014 00:05 UTC |
Last Modified: | 05 Nov 2024 10:24 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/40411 (The current URI for this page, for reference purposes) |
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