Nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols

Construction of C–S bonds via C–H functionalization is an attractive route to organosulfur compounds. Here, the authors show the synergistic combination of NiH-catalysed alkene isomerization and subsequent thiolation to afford remote hydrothiolation products from alkenes (or alkynes) and thiols unde...

Descripción completa

Guardado en:

Detalles Bibliográficos
Autores principales:	Yulong Zhang, Xianfeng Xu, Shaolin Zhu
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2019
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/954cd38c9e4b48aa9b17020e43fde7b9
Etiquetas:	Agregar Etiqueta Sin Etiquetas, Sea el primero en etiquetar este registro!

id	oai:doaj.org-article:954cd38c9e4b48aa9b17020e43fde7b9
record_format	dspace
spelling	oai:doaj.org-article:954cd38c9e4b48aa9b17020e43fde7b92021-12-02T16:57:30ZNickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols10.1038/s41467-019-09783-w2041-1723https://doaj.org/article/954cd38c9e4b48aa9b17020e43fde7b92019-04-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-09783-whttps://doaj.org/toc/2041-1723Construction of C–S bonds via C–H functionalization is an attractive route to organosulfur compounds. Here, the authors show the synergistic combination of NiH-catalysed alkene isomerization and subsequent thiolation to afford remote hydrothiolation products from alkenes (or alkynes) and thiols under mild conditions.Yulong ZhangXianfeng XuShaolin ZhuNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Yulong Zhang Xianfeng Xu Shaolin Zhu Nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols
description	Construction of C–S bonds via C–H functionalization is an attractive route to organosulfur compounds. Here, the authors show the synergistic combination of NiH-catalysed alkene isomerization and subsequent thiolation to afford remote hydrothiolation products from alkenes (or alkynes) and thiols under mild conditions.
format	article
author	Yulong Zhang Xianfeng Xu Shaolin Zhu
author_facet	Yulong Zhang Xianfeng Xu Shaolin Zhu
author_sort	Yulong Zhang
title	Nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols
title_short	Nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols
title_full	Nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols
title_fullStr	Nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols
title_full_unstemmed	Nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols
title_sort	nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols
publisher	Nature Portfolio
publishDate	2019
url	https://doaj.org/article/954cd38c9e4b48aa9b17020e43fde7b9
work_keys_str_mv	AT yulongzhang nickelcatalysedselectivemigratoryhydrothiolationofalkenesandalkyneswiththiols AT xianfengxu nickelcatalysedselectivemigratoryhydrothiolationofalkenesandalkyneswiththiols AT shaolinzhu nickelcatalysedselectivemigratoryhydrothiolationofalkenesandalkyneswiththiols
_version_	1718382515007258624

Nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols

Ejemplares similares