Catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective C-F bond activation

A regioselective carbosilylation of alkenes is a powerful strategy to access functionalized silylated alkanes. In this study, the authors report a catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides, mediated by t BuOK, and synthesise various silylated alkanes with t...

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Autores principales: Jun Zhou, Bingyao Jiang, Yamato Fujihira, Zhengyu Zhao, Takanori Imai, Norio Shibata
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/a518b1524bb44d3fb2732d1225497e4f
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spelling oai:doaj.org-article:a518b1524bb44d3fb2732d1225497e4f2021-12-02T17:40:28ZCatalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective C-F bond activation10.1038/s41467-021-24031-w2041-1723https://doaj.org/article/a518b1524bb44d3fb2732d1225497e4f2021-06-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-24031-whttps://doaj.org/toc/2041-1723A regioselective carbosilylation of alkenes is a powerful strategy to access functionalized silylated alkanes. In this study, the authors report a catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides, mediated by t BuOK, and synthesise various silylated alkanes with tertiary or quaternary carbon centres.Jun ZhouBingyao JiangYamato FujihiraZhengyu ZhaoTakanori ImaiNorio ShibataNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Jun Zhou
Bingyao Jiang
Yamato Fujihira
Zhengyu Zhao
Takanori Imai
Norio Shibata
Catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective C-F bond activation
description A regioselective carbosilylation of alkenes is a powerful strategy to access functionalized silylated alkanes. In this study, the authors report a catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides, mediated by t BuOK, and synthesise various silylated alkanes with tertiary or quaternary carbon centres.
format article
author Jun Zhou
Bingyao Jiang
Yamato Fujihira
Zhengyu Zhao
Takanori Imai
Norio Shibata
author_facet Jun Zhou
Bingyao Jiang
Yamato Fujihira
Zhengyu Zhao
Takanori Imai
Norio Shibata
author_sort Jun Zhou
title Catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective C-F bond activation
title_short Catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective C-F bond activation
title_full Catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective C-F bond activation
title_fullStr Catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective C-F bond activation
title_full_unstemmed Catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective C-F bond activation
title_sort catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective c-f bond activation
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/a518b1524bb44d3fb2732d1225497e4f
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AT yamatofujihira catalystfreecarbosilylationofalkenesusingsilylboronatesandorganicfluoridesviaselectivecfbondactivation
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AT takanoriimai catalystfreecarbosilylationofalkenesusingsilylboronatesandorganicfluoridesviaselectivecfbondactivation
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