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Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials

A metal-free approach combining sulfoxide-directed metal-free C–H cross-couplings with tuneable electrophile-mediated heterocyclizations and carbocyclative dimerizations, allows expedient access to benzothiophene-based systems that are components of important materials or are proven organic material...

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Detalles Bibliográficos
Autores principales: Eberhart, Andrew J., Shrives, Harry, Zhang, Yuntong, Carrër, Amandine, Parry, Adam V. S., Tate, Daniel J., Turner, Michael L., Procter, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975836/
https://www.ncbi.nlm.nih.gov/pubmed/29910885
http://dx.doi.org/10.1039/c5sc03823e
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author Eberhart, Andrew J.
Shrives, Harry
Zhang, Yuntong
Carrër, Amandine
Parry, Adam V. S.
Tate, Daniel J.
Turner, Michael L.
Procter, David J.
author_facet Eberhart, Andrew J.
Shrives, Harry
Zhang, Yuntong
Carrër, Amandine
Parry, Adam V. S.
Tate, Daniel J.
Turner, Michael L.
Procter, David J.
author_sort Eberhart, Andrew J.
collection PubMed
description A metal-free approach combining sulfoxide-directed metal-free C–H cross-couplings with tuneable electrophile-mediated heterocyclizations and carbocyclative dimerizations, allows expedient access to benzothiophene-based systems that are components of important materials or are proven organic materials in their own right. As benzothiophene-based materials are typically prepared using Pd-catalyzed cross-coupling processes, our approach allows potential issues of metal cost and supply, and metal-contamination of products, to be avoided.
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spelling pubmed-59758362018-06-15 Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials Eberhart, Andrew J. Shrives, Harry Zhang, Yuntong Carrër, Amandine Parry, Adam V. S. Tate, Daniel J. Turner, Michael L. Procter, David J. Chem Sci Chemistry A metal-free approach combining sulfoxide-directed metal-free C–H cross-couplings with tuneable electrophile-mediated heterocyclizations and carbocyclative dimerizations, allows expedient access to benzothiophene-based systems that are components of important materials or are proven organic materials in their own right. As benzothiophene-based materials are typically prepared using Pd-catalyzed cross-coupling processes, our approach allows potential issues of metal cost and supply, and metal-contamination of products, to be avoided. Royal Society of Chemistry 2016-02-01 2015-11-09 /pmc/articles/PMC5975836/ /pubmed/29910885 http://dx.doi.org/10.1039/c5sc03823e Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Eberhart, Andrew J.
Shrives, Harry
Zhang, Yuntong
Carrër, Amandine
Parry, Adam V. S.
Tate, Daniel J.
Turner, Michael L.
Procter, David J.
Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials
title Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials
title_full Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials
title_fullStr Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials
title_full_unstemmed Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials
title_short Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials
title_sort sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975836/
https://www.ncbi.nlm.nih.gov/pubmed/29910885
http://dx.doi.org/10.1039/c5sc03823e
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