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Challenges and opportunities for alkane functionalisation using molecular catalysts

The conversion of vast low-value saturated hydrocarbons into valuable chemicals is of great interest. Thanks to the progression of organometallic and coordination chemistry, transition metal catalysed C sp(3)–H bond functionalisation has now become a powerful tool for alkane transformations. Specifi...

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Detalles Bibliográficos
Autores principales: Tang, Xinxin, Jia, Xiangqing, Huang, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870200/
https://www.ncbi.nlm.nih.gov/pubmed/29629098
http://dx.doi.org/10.1039/c7sc03610h
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author Tang, Xinxin
Jia, Xiangqing
Huang, Zheng
author_facet Tang, Xinxin
Jia, Xiangqing
Huang, Zheng
author_sort Tang, Xinxin
collection PubMed
description The conversion of vast low-value saturated hydrocarbons into valuable chemicals is of great interest. Thanks to the progression of organometallic and coordination chemistry, transition metal catalysed C sp(3)–H bond functionalisation has now become a powerful tool for alkane transformations. Specifically, methods for alkane functionalisation include radical initiated C–H functionalisation, carbene/nitrene insertion, and transition metal catalysed C–H bond activation. This perspective provides a systematic and concise overview of each protocol, highlighting the factors that govern regioselectivity in these reactions. The challenges of the existing catalytic tactics and future directions for catalyst development in this field will be presented.
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spelling pubmed-58702002018-04-06 Challenges and opportunities for alkane functionalisation using molecular catalysts Tang, Xinxin Jia, Xiangqing Huang, Zheng Chem Sci Chemistry The conversion of vast low-value saturated hydrocarbons into valuable chemicals is of great interest. Thanks to the progression of organometallic and coordination chemistry, transition metal catalysed C sp(3)–H bond functionalisation has now become a powerful tool for alkane transformations. Specifically, methods for alkane functionalisation include radical initiated C–H functionalisation, carbene/nitrene insertion, and transition metal catalysed C–H bond activation. This perspective provides a systematic and concise overview of each protocol, highlighting the factors that govern regioselectivity in these reactions. The challenges of the existing catalytic tactics and future directions for catalyst development in this field will be presented. Royal Society of Chemistry 2017-11-09 /pmc/articles/PMC5870200/ /pubmed/29629098 http://dx.doi.org/10.1039/c7sc03610h Text en This journal is © The Royal Society of Chemistry 2018 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Tang, Xinxin
Jia, Xiangqing
Huang, Zheng
Challenges and opportunities for alkane functionalisation using molecular catalysts
title Challenges and opportunities for alkane functionalisation using molecular catalysts
title_full Challenges and opportunities for alkane functionalisation using molecular catalysts
title_fullStr Challenges and opportunities for alkane functionalisation using molecular catalysts
title_full_unstemmed Challenges and opportunities for alkane functionalisation using molecular catalysts
title_short Challenges and opportunities for alkane functionalisation using molecular catalysts
title_sort challenges and opportunities for alkane functionalisation using molecular catalysts
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870200/
https://www.ncbi.nlm.nih.gov/pubmed/29629098
http://dx.doi.org/10.1039/c7sc03610h
work_keys_str_mv AT tangxinxin challengesandopportunitiesforalkanefunctionalisationusingmolecularcatalysts
AT jiaxiangqing challengesandopportunitiesforalkanefunctionalisationusingmolecularcatalysts
AT huangzheng challengesandopportunitiesforalkanefunctionalisationusingmolecularcatalysts