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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Published in | Tetrahedron letters Vol. 38; no. 5; pp. 777 - 778 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
OXFORD
Elsevier Ltd
03.02.1997
Elsevier |
Subjects | |
Online Access | Get full text |
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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 |