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

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

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

Chemistry

Research output: Contribution to journal › Article › peer-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 language	English (US)
Pages (from-to)	3445-3448
Number of pages	4
Journal	Tetrahedron Letters
Volume	27
Issue number	30
DOIs	https://doi.org/10.1016/S0040-4039(00)84818-2
State	Published - 1986

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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

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

author = "Thomas Rauchfuss and Zank, {Gregg A.}",

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volume = "27",

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AU - Rauchfuss, Thomas

AU - Zank, Gregg A.

PY - 1986

Y1 - 1986

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

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EP - 3448

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

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ER -

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

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