Challenges and opportunities for alkane functionalisation using molecular catalysts

被引:79
|
作者
Tang, Xinxin [1 ]
Jia, Xiangqing [1 ]
Huang, Zheng [1 ]
机构
[1] Chinese Acad Sci, State Key Lab Organomet Chem, Shanghai Inst Organ Chem, Univ Chinese Acad Sci, 345 Lingling Rd, Shanghai 200032, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
C-H-BONDS; ACCEPTOR PINCER CHEMISTRY; IRIDIUM COMPLEXES; TRANSFER DEHYDROGENATION; SATURATED-HYDROCARBONS; SELECTIVE FUNCTIONALIZATION; UNACTIVATED ALKANES; CARBENE INSERTION; METAL-COMPLEXES; CHLORIDE COMPLEXES;
D O I
10.1039/c7sc03610h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:288 / 299
页数:12
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