Manganese-Catalyzed C(sp2)-H Addition to Polar Unsaturated Bonds

被引:7
作者
Liu, Ting [1 ,2 ]
Wang, Congyang [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, CAS Res Educ Ctr Excellence Mol Sci, Inst Chem, Beijing Natl Lab Mol Sci,CAS Key Lab Mol Recognit, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Huairou Natl Comprehens Sci Ctr, Phys Sci Lab, Beijing 101400, Peoples R China
基金
中国国家自然科学基金;
关键词
manganese; catalysis; C-H activation; polar unsaturated bonds; organic synthesis; H CONJUGATE ADDITION; IMINES; ENAMINYLATION; ALKENYLATION; METALATION; ACTIVATION; ALDEHYDES; KETONES; ALKYNES; ACCESS;
D O I
10.1055/a-1468-6136
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Transition-metal-catalyzed nucleophilic C-H addition of hydrocarbons to polar unsaturated bonds could intrinsically avoid prefunctionalization of substrates and formation of waste byproducts, thus featuring high step- and atom-economy. As the third most abundant transition metal, manganese-catalyzed C-H addition to polar unsaturated bonds remains challenging, partially due to the difficulty in building a closed catalytic cycle of manganese. In the past few years, we have developed manganese catalysis to enable the sp2-hydrid C-H addition to polar unsaturated bonds (e.g., imines, aldehydes, nitriles), which will be discussed in this personal account.
引用
收藏
页码:1323 / 1329
页数:7
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