A highly diastereoselective electrochemical epoxidation

The electrochemical epoxidation of 3 gives the Merck HIV-protease inhibitor, Indinavir Sulfate, intermediate 1 in high yield and diastereoselectivity in an operationally simple procedure. Electrochemical epoxidation of 3 gives the Merck HIV-protease inhibitor (Indinavir Sulfate) intermediate 1 in hi...

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Bibliographic Details
Published inTetrahedron letters Vol. 38; no. 5; pp. 777 - 778
Main Authors Rossen, K., Volante, R.P., Reider, P.J.
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 03.02.1997
Elsevier
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Summary:The electrochemical epoxidation of 3 gives the Merck HIV-protease inhibitor, Indinavir Sulfate, intermediate 1 in high yield and diastereoselectivity in an operationally simple procedure. Electrochemical epoxidation of 3 gives the Merck HIV-protease inhibitor (Indinavir Sulfate) intermediate 1 in high yield and diastereoselectivity in an operationally simple procedure.
ISSN:0040-4039
1873-3581
DOI:10.1016/S0040-4039(96)02445-8