Issue 14, 1994

Azasulfonamidopeptides as peptide bond hydrolysis transition state analogues. Part 2. Potential HIV-1 proteinase inhibitor

Abstract

The synthesis of [N-benzyl-N′-(Nα-benzyloxycarbonyl-L-asparaginyl)hydrazino]sulfonyl-L-prolyl-L-isoleucyl-L-valine methyl ester 4, a potential HIV-1 proteinase inhibitor, is described.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 1953-1955

Azasulfonamidopeptides as peptide bond hydrolysis transition state analogues. Part 2. Potential HIV-1 proteinase inhibitor

T. J. Cheeseright, S. Daenke, D. T. Elmore and J. H. Jones, J. Chem. Soc., Perkin Trans. 1, 1994, 1953 DOI: 10.1039/P19940001953

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