A highly diastereoselective electrochemical epoxidation

K. Rossen, R. P. Volante, P. J. Reider

Research output: Contribution to journalArticle

14 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)777-778
Number of pages2
JournalTetrahedron Letters
Volume38
Issue number5
DOIs
StatePublished - Feb 3 1997
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Fingerprint Dive into the research topics of 'A highly diastereoselective electrochemical epoxidation'. Together they form a unique fingerprint.

  • Cite this