Nickel(ii)-catalyzed tandem C(sp(2))–H bond activation and annulation of arenes with gem-dibromoalkenes

A nickel(ii)/silver(i)-catalyzed tandem C(sp(2))–H activation and intramolecular annulation of arenes with dibromoalkenes has been successfully achieved, which offers an efficient approach to the 3-methyleneisoindolin-1-one scaffold. Attractive features of this system include its low cost, ease of o...

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Detalles Bibliográficos
Autores principales: Shi, Yun, Li, Meng-Sheng, Zhang, Fangdong, Chen, Baohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092601/
https://www.ncbi.nlm.nih.gov/pubmed/35558433
http://dx.doi.org/10.1039/c8ra03278e
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author Shi, Yun
Li, Meng-Sheng
Zhang, Fangdong
Chen, Baohua
author_facet Shi, Yun
Li, Meng-Sheng
Zhang, Fangdong
Chen, Baohua
author_sort Shi, Yun
collection PubMed
description A nickel(ii)/silver(i)-catalyzed tandem C(sp(2))–H activation and intramolecular annulation of arenes with dibromoalkenes has been successfully achieved, which offers an efficient approach to the 3-methyleneisoindolin-1-one scaffold. Attractive features of this system include its low cost, ease of operation, and its ability to access a wide range of isoindolinones.
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spelling pubmed-90926012022-05-11 Nickel(ii)-catalyzed tandem C(sp(2))–H bond activation and annulation of arenes with gem-dibromoalkenes Shi, Yun Li, Meng-Sheng Zhang, Fangdong Chen, Baohua RSC Adv Chemistry A nickel(ii)/silver(i)-catalyzed tandem C(sp(2))–H activation and intramolecular annulation of arenes with dibromoalkenes has been successfully achieved, which offers an efficient approach to the 3-methyleneisoindolin-1-one scaffold. Attractive features of this system include its low cost, ease of operation, and its ability to access a wide range of isoindolinones. The Royal Society of Chemistry 2018-08-13 /pmc/articles/PMC9092601/ /pubmed/35558433 http://dx.doi.org/10.1039/c8ra03278e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Shi, Yun
Li, Meng-Sheng
Zhang, Fangdong
Chen, Baohua
Nickel(ii)-catalyzed tandem C(sp(2))–H bond activation and annulation of arenes with gem-dibromoalkenes
title Nickel(ii)-catalyzed tandem C(sp(2))–H bond activation and annulation of arenes with gem-dibromoalkenes
title_full Nickel(ii)-catalyzed tandem C(sp(2))–H bond activation and annulation of arenes with gem-dibromoalkenes
title_fullStr Nickel(ii)-catalyzed tandem C(sp(2))–H bond activation and annulation of arenes with gem-dibromoalkenes
title_full_unstemmed Nickel(ii)-catalyzed tandem C(sp(2))–H bond activation and annulation of arenes with gem-dibromoalkenes
title_short Nickel(ii)-catalyzed tandem C(sp(2))–H bond activation and annulation of arenes with gem-dibromoalkenes
title_sort nickel(ii)-catalyzed tandem c(sp(2))–h bond activation and annulation of arenes with gem-dibromoalkenes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092601/
https://www.ncbi.nlm.nih.gov/pubmed/35558433
http://dx.doi.org/10.1039/c8ra03278e
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