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https://doi.org/10.1080/00397919608003563
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Cite Journal: Synthetic Communications |  Publication Date: Jun 1, 1996 |
 Citations: 3 |
Affiliation: Indian Institute of Chemical Technology
Abstract Regioselective opening of the aziridine ring in the carbohydrate-based precursor led to the stereoselective synthesis of N-Boc-O-benzyl-(4S,5S)-5-amino-4-hydroxy-6-phenylhexanoic acid methyl ester, the hydroxyethylene dipeptide isostere moiety of potent HIV-1 protease inhibitor.
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