Mechanistic studies on the thiation of carbonyls by Lawesson's reagent: The role of a 3-coordinate phosphorus(V) species.

Thomas Rauchfuss, Gregg A. Zank

Research output: Contribution to journalArticlepeer-review

Abstract

Structural, kinetic, and spectroscopic studies show that the mechanism for the thiation of organic carbonyls by Lawesson's reagent involves momomeric RPS2 intermediates.

Original languageEnglish (US)
Pages (from-to)3445-3448
Number of pages4
JournalTetrahedron Letters
Volume27
Issue number30
DOIs
StatePublished - 1986

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Mechanistic studies on the thiation of carbonyls by Lawesson's reagent: The role of a 3-coordinate phosphorus(V) species.'. Together they form a unique fingerprint.

Cite this