A highly diastereoselective electrochemical epoxidation

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

Research output: Contribution to journalArticlepeer-review

23 Scopus citations


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
Issue number5
StatePublished - Feb 3 1997
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry


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