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Ni-catalysed reductive arylalkylation of unactivated alkenes

In this protocol Ni-catalysed reductive arylalkylation of unactivated alkenes tethered to aryl bromides with primary alkyl bromides has been accomplished, providing a new path to construct diverse benzene-fused carbo- and heterocyclic cores including indanes, tetrahydroisoquinolines, indolines and i...

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Detalles Bibliográficos
Autores principales: Jin, Youxiang, Wang, Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369408/
https://www.ncbi.nlm.nih.gov/pubmed/30842845
http://dx.doi.org/10.1039/c8sc04279a
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author Jin, Youxiang
Wang, Chuan
author_facet Jin, Youxiang
Wang, Chuan
author_sort Jin, Youxiang
collection PubMed
description In this protocol Ni-catalysed reductive arylalkylation of unactivated alkenes tethered to aryl bromides with primary alkyl bromides has been accomplished, providing a new path to construct diverse benzene-fused carbo- and heterocyclic cores including indanes, tetrahydroisoquinolines, indolines and isochromanes. Notably, this new method circumvents the pregeneration of organometallics and demonstrates high tolerance to a wide range of functional groups. The preliminary mechanistic investigations suggest a reaction pathway with an intermediate reduction.
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spelling pubmed-63694082019-03-06 Ni-catalysed reductive arylalkylation of unactivated alkenes Jin, Youxiang Wang, Chuan Chem Sci Chemistry In this protocol Ni-catalysed reductive arylalkylation of unactivated alkenes tethered to aryl bromides with primary alkyl bromides has been accomplished, providing a new path to construct diverse benzene-fused carbo- and heterocyclic cores including indanes, tetrahydroisoquinolines, indolines and isochromanes. Notably, this new method circumvents the pregeneration of organometallics and demonstrates high tolerance to a wide range of functional groups. The preliminary mechanistic investigations suggest a reaction pathway with an intermediate reduction. Royal Society of Chemistry 2018-12-04 /pmc/articles/PMC6369408/ /pubmed/30842845 http://dx.doi.org/10.1039/c8sc04279a Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Jin, Youxiang
Wang, Chuan
Ni-catalysed reductive arylalkylation of unactivated alkenes
title Ni-catalysed reductive arylalkylation of unactivated alkenes
title_full Ni-catalysed reductive arylalkylation of unactivated alkenes
title_fullStr Ni-catalysed reductive arylalkylation of unactivated alkenes
title_full_unstemmed Ni-catalysed reductive arylalkylation of unactivated alkenes
title_short Ni-catalysed reductive arylalkylation of unactivated alkenes
title_sort ni-catalysed reductive arylalkylation of unactivated alkenes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369408/
https://www.ncbi.nlm.nih.gov/pubmed/30842845
http://dx.doi.org/10.1039/c8sc04279a
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