Cobalt(II) Porphyrin-Catalyzed Intramolecular Cyclopropanation of N-Alkyl Indoles/Pyrroles with Alkylcarbene: Efficient Synthesis of Polycyclic N-Heterocycles

被引:69
作者
Reddy, Annapureddy Rajasekar [1 ,2 ,3 ]
Hao, Fei [1 ,2 ,3 ]
Wu, Kai [1 ,2 ,3 ]
Zhou, Cong-Ying [1 ,2 ,3 ]
Che, Chi-Ming [1 ,2 ,3 ]
机构
[1] HKU Shenzhen Inst Res & Innovat, Shenzhen, Peoples R China
[2] Univ Hong Kong, State Key Lab Synthet Chem, Pokfulam Rd, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Dept Chem, Pokfulam Rd, Hong Kong, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
carbenes; cobalt; fused-ring systems; heterocycles; porphyrinoids; C-H FUNCTIONALIZATION; CHIRAL IRIDIUM(III) COMPLEX; GENERATED IN-SITU; DIAZO-COMPOUNDS; STEREOSELECTIVE-SYNTHESIS; CARBENE INSERTION; INDOLE ALKALOIDS; TOSYLHYDRAZONES; REAGENTS; BONDS;
D O I
10.1002/anie.201506418
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A protocol on chemoselective cobalt(II) porphyrin-catalyzed intramolecular cyclopropanation of N-alkyl indoles/pyrroles with alkylcarbenes has been developed. The reaction enables the rapid construction of a range of nitrogen-containing polycyclic compounds in moderate to high yields from readily accessible materials. These N-containing polycyclic compounds can be converted into a variety of N-heterocycles with potential synthetic and biological interest. Compared to their N-tosylhydrazone counterparts, the use of bulky N-2,4,6-triisopropylbenzenesulfonyl hydrazones as carbene precursors allows cyclopropanation to occur under milder reaction conditions.
引用
收藏
页码:1810 / 1815
页数:6
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