Stereoselective synthesis of β-substituted phenylalanine-β-phenylisoserine-derived tripeptides using N-cinnamoyl-l-proline as template: synthesis of structural analogues of HIV protease inhibitors

Saha, Biswajit ; Nandy, Jyoti Prokash ; Shukla, Shalini ; Siddiqui, Iffat ; Iqbal, Javed (2002) Stereoselective synthesis of β-substituted phenylalanine-β-phenylisoserine-derived tripeptides using N-cinnamoyl-l-proline as template: synthesis of structural analogues of HIV protease inhibitors Journal of Organic Chemistry, 67 (22). pp. 7858-7860. ISSN 0022-3263

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Official URL: http://pubs.acs.org/doi/abs/10.1021/jo0109826

Related URL: http://dx.doi.org/10.1021/jo0109826

Abstract

N-Cinnamoyl-L-proline can be used as a template on which β-substituted phenylalanine and β-phenylisoserine residues can be synthesized leading to tripeptide derivatives as structural analogues of HIV protease inhibitors.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:16978
Deposited On:16 Nov 2010 13:12
Last Modified:17 Feb 2011 04:55

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