Intramolecular Csp3-H/C-C bond amination of alkyl azides for the selective synthesis of cyclic imines and tertiary amines

被引:14
|
作者
Wen, Xiaojin [1 ]
Li, Xinyao [1 ]
Luo, Xiao [1 ]
Wang, Weijin [1 ]
Song, Song [1 ,2 ]
Jiao, Ning [1 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
C-H AMINATION; SCHMIDT REACTION; RING-EXPANSION; CHEMOSELECTIVE AMINATION; EFFICIENT SYNTHESIS; C(SP(3))-H BONDS; HYDROXY AZIDES; ORGANIC AZIDES; NITROGEN; FUNCTIONALIZATION;
D O I
10.1039/c9sc05522c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The intramolecular Csp(3)-H and/or C-C bond amination is very important in modern organic synthesis due to its efficiency in the construction of diversified N-heterocycles. Herein, we report a novel intramolecular cyclization of alkyl azides for the synthesis of cyclic imines and tertiary amines through selective Csp(3)-H and/or C-C bond cleavage. Two C-N single bonds or a C=N double bond are efficiently constructed in these transformations. The carbocation mechanism differs from the reported metal nitrene intermediates and therefore enables metal-free and new transformation.
引用
收藏
页码:4482 / 4487
页数:6
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