Nickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide

In contrast to the well-established palladium-catalyzed version, the nickel-catalyzed carbonylative coupling is underdeveloped. Here the authors report a nickel-catalyzed allylic carbonylative coupling with alkyl zinc reagents, allowing for preparation of β,γ-unsaturated ketones in a linear-selectiv...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Yangyang Weng, Chenhuan Zhang, Zaiquan Tang, Mohini Shrestha, Wenyi Huang, Jingping Qu, Yifeng Chen
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2020
Materias:
Q
Acceso en línea:https://doaj.org/article/48391b364a9c447590575e70c4ce619c
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:48391b364a9c447590575e70c4ce619c
record_format dspace
spelling oai:doaj.org-article:48391b364a9c447590575e70c4ce619c2021-12-02T14:40:39ZNickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide10.1038/s41467-020-14320-12041-1723https://doaj.org/article/48391b364a9c447590575e70c4ce619c2020-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-14320-1https://doaj.org/toc/2041-1723In contrast to the well-established palladium-catalyzed version, the nickel-catalyzed carbonylative coupling is underdeveloped. Here the authors report a nickel-catalyzed allylic carbonylative coupling with alkyl zinc reagents, allowing for preparation of β,γ-unsaturated ketones in a linear-selective fashion.Yangyang WengChenhuan ZhangZaiquan TangMohini ShresthaWenyi HuangJingping QuYifeng ChenNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Yangyang Weng
Chenhuan Zhang
Zaiquan Tang
Mohini Shrestha
Wenyi Huang
Jingping Qu
Yifeng Chen
Nickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide
description In contrast to the well-established palladium-catalyzed version, the nickel-catalyzed carbonylative coupling is underdeveloped. Here the authors report a nickel-catalyzed allylic carbonylative coupling with alkyl zinc reagents, allowing for preparation of β,γ-unsaturated ketones in a linear-selective fashion.
format article
author Yangyang Weng
Chenhuan Zhang
Zaiquan Tang
Mohini Shrestha
Wenyi Huang
Jingping Qu
Yifeng Chen
author_facet Yangyang Weng
Chenhuan Zhang
Zaiquan Tang
Mohini Shrestha
Wenyi Huang
Jingping Qu
Yifeng Chen
author_sort Yangyang Weng
title Nickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide
title_short Nickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide
title_full Nickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide
title_fullStr Nickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide
title_full_unstemmed Nickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide
title_sort nickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/48391b364a9c447590575e70c4ce619c
work_keys_str_mv AT yangyangweng nickelcatalyzedallyliccarbonylativecouplingofalkylzincreagentswithtertbutylisocyanide
AT chenhuanzhang nickelcatalyzedallyliccarbonylativecouplingofalkylzincreagentswithtertbutylisocyanide
AT zaiquantang nickelcatalyzedallyliccarbonylativecouplingofalkylzincreagentswithtertbutylisocyanide
AT mohinishrestha nickelcatalyzedallyliccarbonylativecouplingofalkylzincreagentswithtertbutylisocyanide
AT wenyihuang nickelcatalyzedallyliccarbonylativecouplingofalkylzincreagentswithtertbutylisocyanide
AT jingpingqu nickelcatalyzedallyliccarbonylativecouplingofalkylzincreagentswithtertbutylisocyanide
AT yifengchen nickelcatalyzedallyliccarbonylativecouplingofalkylzincreagentswithtertbutylisocyanide
_version_ 1718390171571847168