Synthesis of 2-Benzazepines from Benzylamines and MBH Adducts Under Rhodium(III) Catalysis via C(sp2)-H Functionalization

被引:40
作者
Pandey, Ashok Kumar [1 ]
Han, Sang Hoon [1 ]
Mishra, Neeraj Kumar [1 ]
Kang, Dahye [2 ,3 ]
Lee, Suk Hun [1 ]
Chun, Rina [1 ]
Hong, Sungwoo [2 ,3 ]
Park, Jung Su [4 ]
Kim, In Su [1 ]
机构
[1] Sungkyunkwan Univ, Sch Pharm, Suwon 16419, South Korea
[2] Inst for Basic Sci Korea, Ctr Catalyt Hydrocarbon Functionalizat, Daejeon 34141, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
[4] Sookmyung Womens Univ, Dept Chem, Seoul 04310, South Korea
来源
ACS CATALYSIS | 2018年 / 8卷 / 01期
基金
新加坡国家研究基金会;
关键词
benzazepines; benzylamines; C-H activation; Morita-Baylis-Hillman adducts; rhodium; BAYLIS-HILLMAN REACTION; C-H ALKYLATION; DENSITY FUNCTIONALS; AZOBENZENES; CYCLIZATION; ALKENYLATION; DERIVATIVES; ALLYLATION; ACTIVATION; DISCOVERY;
D O I
10.1021/acscatal.7b03812
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The rhodium(III)-catalyzed cross-coupling reaction between commercially available benzylamines and Morita-Baylis--Hillman (MBH) adducts is described. This protocol provides a facile access to various 2-benzazepine derivatives via the C(sp(2))-H activation of N-allylated benzylamines and subsequent intramolecular olefin insertion followed by N-allylation reaction. A range of substrates has been used, and a high level of chemoselectivity as well as functional group tolerance was observed. To gain mechanistic insight of this transformation, DFT performed. calculations were also performed.
引用
收藏
页码:742 / 746
页数:5
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