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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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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. |
format | Online Article Text |
id | pubmed-6259452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT eichmanchadc transitionmetalcatalyzedsynthesisofarylsulfides AT stambulijamesp transitionmetalcatalyzedsynthesisofarylsulfides |