MECHANISTIC STUDIES ON THE THIATION OF CARBONYLS BY LAWESSON'S REAGENT: THE ROLE OF A 3-COORDINATE PHOSPHORUS(V) SPECIES.

DOI: 10.1016/S0040-4039(00)84818-2

Source and publish data:

Tetrahedron Letters p. 3445 - 3448 (1986)

Update date:2022-08-11

Topics:

Authors:

Rauchfuss, Thomas B.

Zank, Gregg A.

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Article abstract of DOI:10.1016/S0040-4039(00)84818-2

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

Full text of DOI:10.1016/S0040-4039(00)84818-2

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