A highly diastereoselective electrochemical epoxidation

DOI: 10.1016/S0040-4039(96)02445-8

Source and publish data:

Tetrahedron Letters p. 777 - 778 (1997)

Update date:2022-08-30

Topics:

Authors:

Rossen Rossen

Volante Volante

Reider Reider

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Article abstract of DOI:10.1016/S0040-4039(96)02445-8

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.

Full text of DOI:10.1016/S0040-4039(96)02445-8

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