Lewis acid catalyzed diastereoselective [3+4]-annulation of donor–acceptor cyclopropanes with anthranils: synthesis of tetrahydro-1-benzazepine derivatives

2017 ◽  
Vol 53 (61) ◽  
pp. 8521-8524 ◽  
Author(s):  
Zhe-Hao Wang ◽  
Huan-Huan Zhang ◽  
Dao-Ming Wang ◽  
Peng-Fei Xu ◽  
Yong-Chun Luo

The [3+4]-annulation between donor–acceptor cyclopropanes and anthranils has been developed for the diastereoselective synthesis of tetrahydro-1-benzazepine derivatives.

2020 ◽  
Vol 22 (5) ◽  
pp. 1903-1907 ◽  
Author(s):  
Bao Qiong Li ◽  
Zong-Wang Qiu ◽  
Ai-Jun Ma ◽  
Jin-Bao Peng ◽  
Na Feng ◽  
...  

Author(s):  
Grzegorz Mlostoń ◽  
Mateusz Kowalczyk ◽  
André U. Augustin ◽  
Peter G. Jones ◽  
Daniel B. Werz

2008 ◽  
Vol 130 (27) ◽  
pp. 8642-8650 ◽  
Author(s):  
Patrick D. Pohlhaus ◽  
Shanina D. Sanders ◽  
Andrew T. Parsons ◽  
Wei Li ◽  
Jeffrey S. Johnson

Synthesis ◽  
2019 ◽  
Vol 52 (02) ◽  
pp. 281-289
Author(s):  
Yerin Kim ◽  
Yong Il Kwon ◽  
Sung-Gon Kim

A method for efficient and mild synthesis of diarylmethylamine scaffold, via Lewis acid catalyzed Friedel–Crafts reaction of donor­–acceptor aziridines with N,N-dialkylanilines to afford a biologically important diarylmethylamine derivatives in high yields (up to 88%), is presented. This reaction is suitable for the synthesis of various diarylmethylamine derivatives and has a broad scope for electron-rich arenes, including dimethoxybenzene.


2020 ◽  
Vol 22 (6) ◽  
pp. 2276-2280 ◽  
Author(s):  
Avishek Guin ◽  
Thukaram Rathod ◽  
Rahul N. Gaykar ◽  
Tony Roy ◽  
Akkattu T. Biju

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