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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-6369408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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
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title_full | Ni-catalysed reductive arylalkylation of unactivated alkenes
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title_fullStr | Ni-catalysed reductive arylalkylation of unactivated alkenes
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title_full_unstemmed | Ni-catalysed reductive arylalkylation of unactivated alkenes
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title_short | Ni-catalysed reductive arylalkylation of unactivated alkenes
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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 |
work_keys_str_mv | AT jinyouxiang nicatalysedreductivearylalkylationofunactivatedalkenes AT wangchuan nicatalysedreductivearylalkylationofunactivatedalkenes |