Stereoselective alkoxycarbonylation of unactivated C(sp3)–H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis

Carbonylation of unactivated C-H bonds is typically carried out on primary C-H sites using gaseous carbon monoxide. Here the authors report a palladium cataylsed alkoxycarbonylation process using alkyl chloroformates that functionalises more challenging unactivated secondary C-H sites.

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Autores principales: Gang Liao, Xue-Song Yin, Kai Chen, Qi Zhang, Shuo-Qing Zhang, Bing-Feng Shi
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/e79fad644ab943149229cbef60c494d5
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spelling oai:doaj.org-article:e79fad644ab943149229cbef60c494d52021-12-02T16:49:41ZStereoselective alkoxycarbonylation of unactivated C(sp3)–H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis10.1038/ncomms129012041-1723https://doaj.org/article/e79fad644ab943149229cbef60c494d52016-09-01T00:00:00Zhttps://doi.org/10.1038/ncomms12901https://doaj.org/toc/2041-1723Carbonylation of unactivated C-H bonds is typically carried out on primary C-H sites using gaseous carbon monoxide. Here the authors report a palladium cataylsed alkoxycarbonylation process using alkyl chloroformates that functionalises more challenging unactivated secondary C-H sites.Gang LiaoXue-Song YinKai ChenQi ZhangShuo-Qing ZhangBing-Feng ShiNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-9 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Gang Liao
Xue-Song Yin
Kai Chen
Qi Zhang
Shuo-Qing Zhang
Bing-Feng Shi
Stereoselective alkoxycarbonylation of unactivated C(sp3)–H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis
description Carbonylation of unactivated C-H bonds is typically carried out on primary C-H sites using gaseous carbon monoxide. Here the authors report a palladium cataylsed alkoxycarbonylation process using alkyl chloroformates that functionalises more challenging unactivated secondary C-H sites.
format article
author Gang Liao
Xue-Song Yin
Kai Chen
Qi Zhang
Shuo-Qing Zhang
Bing-Feng Shi
author_facet Gang Liao
Xue-Song Yin
Kai Chen
Qi Zhang
Shuo-Qing Zhang
Bing-Feng Shi
author_sort Gang Liao
title Stereoselective alkoxycarbonylation of unactivated C(sp3)–H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis
title_short Stereoselective alkoxycarbonylation of unactivated C(sp3)–H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis
title_full Stereoselective alkoxycarbonylation of unactivated C(sp3)–H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis
title_fullStr Stereoselective alkoxycarbonylation of unactivated C(sp3)–H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis
title_full_unstemmed Stereoselective alkoxycarbonylation of unactivated C(sp3)–H bonds with alkyl chloroformates via Pd(II)/Pd(IV) catalysis
title_sort stereoselective alkoxycarbonylation of unactivated c(sp3)–h bonds with alkyl chloroformates via pd(ii)/pd(iv) catalysis
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/e79fad644ab943149229cbef60c494d5
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AT kaichen stereoselectivealkoxycarbonylationofunactivatedcsp3hbondswithalkylchloroformatesviapdiipdivcatalysis
AT qizhang stereoselectivealkoxycarbonylationofunactivatedcsp3hbondswithalkylchloroformatesviapdiipdivcatalysis
AT shuoqingzhang stereoselectivealkoxycarbonylationofunactivatedcsp3hbondswithalkylchloroformatesviapdiipdivcatalysis
AT bingfengshi stereoselectivealkoxycarbonylationofunactivatedcsp3hbondswithalkylchloroformatesviapdiipdivcatalysis
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