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Transition Metal Catalyzed Synthesis of Aryl Sulfides

The presence of aryl sulfides in biologically active compounds has resulted in the development of new methods to form carbon-sulfur bonds. The synthesis of aryl sulfides via metal catalysis has significantly increased in recent years. Historically, thiolates and sulfides have been thought to plague...

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Detalles Bibliográficos
Autores principales: Eichman, Chad C., Stambuli, James P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259452/
https://www.ncbi.nlm.nih.gov/pubmed/21242940
http://dx.doi.org/10.3390/molecules16010590
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author Eichman, Chad C.
Stambuli, James P.
author_facet Eichman, Chad C.
Stambuli, James P.
author_sort Eichman, Chad C.
collection PubMed
description The presence of aryl sulfides in biologically active compounds has resulted in the development of new methods to form carbon-sulfur bonds. The synthesis of aryl sulfides via metal catalysis has significantly increased in recent years. Historically, thiolates and sulfides have been thought to plague catalyst activity in the presence of transition metals. Indeed, strong coordination of thiolates and thioethers to transition metals can often hinder catalytic activity; however, various catalysts are able to withstand catalyst deactivation and form aryl carbon-sulfur bonds in high-yielding transformations. This review discusses the metal-catalyzed arylation of thiols and the use of disulfides as metal-thiolate precursors for the formation of C-S bonds.
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spelling pubmed-62594522018-12-07 Transition Metal Catalyzed Synthesis of Aryl Sulfides Eichman, Chad C. Stambuli, James P. Molecules Review The presence of aryl sulfides in biologically active compounds has resulted in the development of new methods to form carbon-sulfur bonds. The synthesis of aryl sulfides via metal catalysis has significantly increased in recent years. Historically, thiolates and sulfides have been thought to plague catalyst activity in the presence of transition metals. Indeed, strong coordination of thiolates and thioethers to transition metals can often hinder catalytic activity; however, various catalysts are able to withstand catalyst deactivation and form aryl carbon-sulfur bonds in high-yielding transformations. This review discusses the metal-catalyzed arylation of thiols and the use of disulfides as metal-thiolate precursors for the formation of C-S bonds. MDPI 2011-01-17 /pmc/articles/PMC6259452/ /pubmed/21242940 http://dx.doi.org/10.3390/molecules16010590 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Eichman, Chad C.
Stambuli, James P.
Transition Metal Catalyzed Synthesis of Aryl Sulfides
title Transition Metal Catalyzed Synthesis of Aryl Sulfides
title_full Transition Metal Catalyzed Synthesis of Aryl Sulfides
title_fullStr Transition Metal Catalyzed Synthesis of Aryl Sulfides
title_full_unstemmed Transition Metal Catalyzed Synthesis of Aryl Sulfides
title_short Transition Metal Catalyzed Synthesis of Aryl Sulfides
title_sort transition metal catalyzed synthesis of aryl sulfides
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259452/
https://www.ncbi.nlm.nih.gov/pubmed/21242940
http://dx.doi.org/10.3390/molecules16010590
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