Issue 11, 1999
From the journal:

Chemical Communications

Asymmetric dihydroxylation route to a dipeptide isostere of a protease inhibitor: enantioselective synthesis of the core unit of ritonavir

Arun K. Ghosh,   Dongwoo Shin  and  Packiarajan Mathivanan  

Abstract

An enantioselective synthesis of the dipeptide isostere of ritonavir has been accomplished utilizing Sharpless asymmetric hydroxylation as the key step.

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Article information

DOI
https://doi.org/10.1039/A902518I
Article type
Paper

Chem. Commun., 1999, 1025-1026

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Asymmetric dihydroxylation route to a dipeptide isostere of a protease inhibitor: enantioselective synthesis of the core unit of ritonavir

A. K. Ghosh, D. Shin and P. Mathivanan, Chem. Commun., 1999, 1025 DOI: 10.1039/A902518I

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