Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides

Chalcogen-containing compounds find broad application in chemical industry. Here, the authors report a nickel-catalyzed reductive chalcogenation of unactivated alkyl bromides with thiosulfonates and selenosulfonates to access a range of unsymmetrical sulfides and selenides under mild conditions.

Guardado en:

Detalles Bibliográficos
Autores principales:	Yi Fang, Torben Rogge, Lutz Ackermann, Shun-Yi Wang, Shun-Jun Ji
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2018
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/5a6a88e661cd4a629ba139e7e843fa3d
Etiquetas:	Agregar Etiqueta Sin Etiquetas, Sea el primero en etiquetar este registro!

id	oai:doaj.org-article:5a6a88e661cd4a629ba139e7e843fa3d
record_format	dspace
spelling	oai:doaj.org-article:5a6a88e661cd4a629ba139e7e843fa3d2021-12-02T15:34:48ZNickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides10.1038/s41467-018-04646-22041-1723https://doaj.org/article/5a6a88e661cd4a629ba139e7e843fa3d2018-06-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-04646-2https://doaj.org/toc/2041-1723Chalcogen-containing compounds find broad application in chemical industry. Here, the authors report a nickel-catalyzed reductive chalcogenation of unactivated alkyl bromides with thiosulfonates and selenosulfonates to access a range of unsymmetrical sulfides and selenides under mild conditions.Yi FangTorben RoggeLutz AckermannShun-Yi WangShun-Jun JiNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Yi Fang Torben Rogge Lutz Ackermann Shun-Yi Wang Shun-Jun Ji Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides
description	Chalcogen-containing compounds find broad application in chemical industry. Here, the authors report a nickel-catalyzed reductive chalcogenation of unactivated alkyl bromides with thiosulfonates and selenosulfonates to access a range of unsymmetrical sulfides and selenides under mild conditions.
format	article
author	Yi Fang Torben Rogge Lutz Ackermann Shun-Yi Wang Shun-Jun Ji
author_facet	Yi Fang Torben Rogge Lutz Ackermann Shun-Yi Wang Shun-Jun Ji
author_sort	Yi Fang
title	Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides
title_short	Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides
title_full	Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides
title_fullStr	Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides
title_full_unstemmed	Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides
title_sort	nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides
publisher	Nature Portfolio
publishDate	2018
url	https://doaj.org/article/5a6a88e661cd4a629ba139e7e843fa3d
work_keys_str_mv	AT yifang nickelcatalyzedreductivethiolationandselenylationofunactivatedalkylbromides AT torbenrogge nickelcatalyzedreductivethiolationandselenylationofunactivatedalkylbromides AT lutzackermann nickelcatalyzedreductivethiolationandselenylationofunactivatedalkylbromides AT shunyiwang nickelcatalyzedreductivethiolationandselenylationofunactivatedalkylbromides AT shunjunji nickelcatalyzedreductivethiolationandselenylationofunactivatedalkylbromides
_version_	1718386720138854400

Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides

Ejemplares similares