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

  • External authors:
  • Andrew J. Eberhart
  • Harry Shrives
  • Yuntong Zhang
  • Amandine Carrër
  • Daniel J. Tate

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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.

In: Chemical Science, Vol. 7, No. 2, 2016, p. 1281-1285.

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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. / Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials. In: Chemical Science. 2016 ; Vol. 7, No. 2. pp. 1281-1285.

Bibtex

@article{cbd09f074a994a479668b02e5b8b90ab,
title = "Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials",
abstract = "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.",
author = "Eberhart, {Andrew J.} and Harry Shrives and Yuntong Zhang and Amandine Carr{\"e}r and Parry, {Adam V S} and Tate, {Daniel J.} and Turner, {Michael L.} and Procter, {David J.}",
year = "2016",
doi = "10.1039/C5SC03823E",
language = "English",
volume = "7",
pages = "1281--1285",
journal = "Chemical Science",
issn = "2041-6520",
publisher = "Royal Society of Chemistry",
number = "2",

}

RIS

TY - JOUR

T1 - Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials

AU - Eberhart, Andrew J.

AU - Shrives, Harry

AU - Zhang, Yuntong

AU - Carrër, Amandine

AU - Parry, Adam V S

AU - Tate, Daniel J.

AU - Turner, Michael L.

AU - Procter, David J.

PY - 2016

Y1 - 2016

N2 - 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.

AB - 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.

UR - http://www.scopus.com/inward/record.url?scp=84961335990&partnerID=8YFLogxK

U2 - 10.1039/C5SC03823E

DO - 10.1039/C5SC03823E

M3 - Article

VL - 7

SP - 1281

EP - 1285

JO - Chemical Science

JF - Chemical Science

SN - 2041-6520

IS - 2

ER -