Manganese-Catalyzed [3+2] Cyclization of Ketones and Isocyanates via Inert C-H Activation

被引:17
|
作者
Huo, Jiaqi [1 ,2 ]
Yang, Yunhui [1 ,2 ,3 ]
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
FUNCTIONALIZATIONS; DERIVATIVES; METALATION; INDOLES; ALKYNES; ESTERS; ACID; KEY;
D O I
10.1021/acs.orglett.1c00857
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Stoichiometric cyclomanganation of aromatic ketones and further reactions of the thus-formed manganacycles with isocyanates were first reported by Kaesz and Liebeskind in 1975 and 1990, respectively. The buildup of a closed manganese catalytic cycle for the reaction of ketones and isocyanates remains an unsolved problem. Herein, an unprecedented trio of Me2Zn/ AlCl3/AgOTf is developed to build up manganese catalysis, which enables the [3 + 2] cyclization of ketones with isocyanates via inert C-H activation to access 3-alkylidene phthalimidines in a straightforward manner unachieved by other transition metal catalyses.
引用
收藏
页码:3384 / 3388
页数:5
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