Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS(2)

A highly efficient and chemoselective method for the synthesis of diaryl disulfides is developed via a visible light-promoted coupling of readily accessible arenediazonium tetrafluoroborates and CS(2). This practical and convenient protocol provides a direct pathway for the assembly of a series of d...

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Detalles Bibliográficos
Autores principales: Leng, Jing, Wang, Shi-Meng, Qin, Hua-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2017
Materias:
Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480343/
https://www.ncbi.nlm.nih.gov/pubmed/28684971
http://dx.doi.org/10.3762/bjoc.13.91
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author Leng, Jing
Wang, Shi-Meng
Qin, Hua-Li
author_facet Leng, Jing
Wang, Shi-Meng
Qin, Hua-Li
author_sort Leng, Jing
collection PubMed
description A highly efficient and chemoselective method for the synthesis of diaryl disulfides is developed via a visible light-promoted coupling of readily accessible arenediazonium tetrafluoroborates and CS(2). This practical and convenient protocol provides a direct pathway for the assembly of a series of disulfides in an environmentally friendly manner with good to excellent yields.
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spelling pubmed-54803432017-07-06 Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS(2) Leng, Jing Wang, Shi-Meng Qin, Hua-Li Beilstein J Org Chem Letter A highly efficient and chemoselective method for the synthesis of diaryl disulfides is developed via a visible light-promoted coupling of readily accessible arenediazonium tetrafluoroborates and CS(2). This practical and convenient protocol provides a direct pathway for the assembly of a series of disulfides in an environmentally friendly manner with good to excellent yields. Beilstein-Institut 2017-05-15 /pmc/articles/PMC5480343/ /pubmed/28684971 http://dx.doi.org/10.3762/bjoc.13.91 Text en Copyright © 2017, Leng et al. https://creativecommons.org/licenses/by/4.0https://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/4.0), 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 Letter
Leng, Jing
Wang, Shi-Meng
Qin, Hua-Li
Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS(2)
title Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS(2)
title_full Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS(2)
title_fullStr Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS(2)
title_full_unstemmed Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS(2)
title_short Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS(2)
title_sort chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and cs(2)
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480343/
https://www.ncbi.nlm.nih.gov/pubmed/28684971
http://dx.doi.org/10.3762/bjoc.13.91
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