Efficiency of a ruthenium catalyst in metathesis reactions of sulfur-containing compounds

Gaëlle Spagnol; Marie Pierre Heck; Steven P. Nolan; Charles Mioskowski

doi:10.1021/ol025834w

Efficiency of a ruthenium catalyst in metathesis reactions of sulfur-containing compounds

Gaëlle Spagnol, Marie Pierre Heck, Steven P. Nolan, Charles Mioskowski

Research output: Contribution to journal › Article › peer-review

89 Scopus citations

Abstract

1,3-Dimesitylimidazol-2-ylidene ruthenium benzylidene catalyst (RuCl₂(=C(H)Ph)(PCy₃)(IMes)) has been successfully employed in ring-closing metathesis reactions of acyclic diene sulfides, disulfides, and dithianes and in self-cross metathesis reactions of ene-sulfides, thioethers and thiols.

Original language	English (US)
Pages (from-to)	1767-1770
Number of pages	4
Journal	Organic Letters
Volume	4
Issue number	10
DOIs	https://doi.org/10.1021/ol025834w
State	Published - May 16 2002
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol025834w

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abstract = "1,3-Dimesitylimidazol-2-ylidene ruthenium benzylidene catalyst (RuCl2(=C(H)Ph)(PCy3)(IMes)) has been successfully employed in ring-closing metathesis reactions of acyclic diene sulfides, disulfides, and dithianes and in self-cross metathesis reactions of ene-sulfides, thioethers and thiols.",

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AU - Spagnol, Gaëlle

AU - Heck, Marie Pierre

AU - Nolan, Steven P.

AU - Mioskowski, Charles

PY - 2002/5/16

Y1 - 2002/5/16

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AB - 1,3-Dimesitylimidazol-2-ylidene ruthenium benzylidene catalyst (RuCl2(=C(H)Ph)(PCy3)(IMes)) has been successfully employed in ring-closing metathesis reactions of acyclic diene sulfides, disulfides, and dithianes and in self-cross metathesis reactions of ene-sulfides, thioethers and thiols.

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Efficiency of a ruthenium catalyst in metathesis reactions of sulfur-containing compounds

Abstract

ASJC Scopus subject areas

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