Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions

A straightforward, efficient, and reliable redox catalyst system for the Au(I)/Au(III)-catalyzed Sonogashira cross-coupling reaction of functionalized terminal alkynes with arylboronic acids under mild conditions has been developed.

Detalles Bibliográficos
Autores principales: Qian, Deyun, Zhang, Junliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2011
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135097/
https://www.ncbi.nlm.nih.gov/pubmed/21804876
http://dx.doi.org/10.3762/bjoc.7.92
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author Qian, Deyun
Zhang, Junliang
author_facet Qian, Deyun
Zhang, Junliang
author_sort Qian, Deyun
collection PubMed
description A straightforward, efficient, and reliable redox catalyst system for the Au(I)/Au(III)-catalyzed Sonogashira cross-coupling reaction of functionalized terminal alkynes with arylboronic acids under mild conditions has been developed.
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spelling pubmed-31350972011-07-29 Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions Qian, Deyun Zhang, Junliang Beilstein J Org Chem Full Research Paper A straightforward, efficient, and reliable redox catalyst system for the Au(I)/Au(III)-catalyzed Sonogashira cross-coupling reaction of functionalized terminal alkynes with arylboronic acids under mild conditions has been developed. Beilstein-Institut 2011-06-15 /pmc/articles/PMC3135097/ /pubmed/21804876 http://dx.doi.org/10.3762/bjoc.7.92 Text en Copyright © 2011, Qian and Zhang https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Qian, Deyun
Zhang, Junliang
Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions
title Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions
title_full Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions
title_fullStr Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions
title_full_unstemmed Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions
title_short Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions
title_sort au(i)/au(iii)-catalyzed sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135097/
https://www.ncbi.nlm.nih.gov/pubmed/21804876
http://dx.doi.org/10.3762/bjoc.7.92
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