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.