Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand

Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand

Alkynes are amongst the most valuable functional groups in organic chemistry, however, the preparation of alkyl-substituted alkynes still remains elusive. Here the authors show a nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts.

Guardado en:
Detalles Bibliográficos
Autores principales: Xingjie Zhang, Di Qi, Chenchen Jiao, Xiaopan Liu, Guisheng Zhang
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Science
Q
Acceso en línea:https://doaj.org/article/e7a2d5a6151041a5a7e81494eb88684a
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:e7a2d5a6151041a5a7e81494eb88684a
record_format dspace
spelling oai:doaj.org-article:e7a2d5a6151041a5a7e81494eb88684a2021-12-02T16:28:01ZNickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand10.1038/s41467-021-25222-12041-1723https://doaj.org/article/e7a2d5a6151041a5a7e81494eb88684a2021-08-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-25222-1https://doaj.org/toc/2041-1723Alkynes are amongst the most valuable functional groups in organic chemistry, however, the preparation of alkyl-substituted alkynes still remains elusive. Here the authors show a nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts.Xingjie ZhangDi QiChenchen JiaoXiaopan LiuGuisheng ZhangNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Xingjie Zhang
Di Qi
Chenchen Jiao
Xiaopan Liu
Guisheng Zhang
Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand
description Alkynes are amongst the most valuable functional groups in organic chemistry, however, the preparation of alkyl-substituted alkynes still remains elusive. Here the authors show a nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts.
format article
author Xingjie Zhang
Di Qi
Chenchen Jiao
Xiaopan Liu
Guisheng Zhang
author_facet Xingjie Zhang
Di Qi
Chenchen Jiao
Xiaopan Liu
Guisheng Zhang
author_sort Xingjie Zhang
title Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand
title_short Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand
title_full Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand
title_fullStr Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand
title_full_unstemmed Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand
title_sort nickel-catalyzed deaminative sonogashira coupling of alkylpyridinium salts enabled by nn2 pincer ligand
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/e7a2d5a6151041a5a7e81494eb88684a
work_keys_str_mv AT xingjiezhang nickelcatalyzeddeaminativesonogashiracouplingofalkylpyridiniumsaltsenabledbynn2pincerligand
AT diqi nickelcatalyzeddeaminativesonogashiracouplingofalkylpyridiniumsaltsenabledbynn2pincerligand
AT chenchenjiao nickelcatalyzeddeaminativesonogashiracouplingofalkylpyridiniumsaltsenabledbynn2pincerligand
AT xiaopanliu nickelcatalyzeddeaminativesonogashiracouplingofalkylpyridiniumsaltsenabledbynn2pincerligand
AT guishengzhang nickelcatalyzeddeaminativesonogashiracouplingofalkylpyridiniumsaltsenabledbynn2pincerligand
_version_ 1718383966082301952

Ejemplares similares