scholarly journals Bicyclic Pyrazolidinone Derivatives from Diastereoselective Catalytic [3 + 3]-Cycloaddition Reactions of Enoldiazoacetates with Azomethine Imines

2013 ◽  
Vol 15 (7) ◽  
pp. 1564-1567 ◽  
Author(s):  
Yu Qian ◽  
Peter J. Zavalij ◽  
Wenhao Hu ◽  
Michael P. Doyle
2020 ◽  
Vol 22 (18) ◽  
pp. 7358-7362
Author(s):  
Qing-Yun Fang ◽  
Hai-Shan Jin ◽  
Ru-Bing Wang ◽  
Li-Ming Zhao

2014 ◽  
Vol 16 (15) ◽  
pp. 4004-4007 ◽  
Author(s):  
Juan Du ◽  
Xianxiu Xu ◽  
Yifei Li ◽  
Ling Pan ◽  
Qun Liu

ChemInform ◽  
2016 ◽  
Vol 47 (51) ◽  
Author(s):  
Amanda Bongers ◽  
Indee Ranasinghe ◽  
Philippe Lemire ◽  
Alyssa Perozzo ◽  
Jean-Francois Vincent-Rocan ◽  
...  

Heterocycles ◽  
2010 ◽  
Vol 81 (7) ◽  
pp. 1669 ◽  
Author(s):  
Hiroyuki Suga ◽  
Tadashi Arikawa ◽  
Kennosuke Itoh ◽  
Yukihisa Okumura ◽  
Akikazu Kakehi ◽  
...  

2016 ◽  
Vol 52 (9) ◽  
pp. 627-636 ◽  
Author(s):  
Nataliya P. Belskaya ◽  
Vasiliy A. Bakulev ◽  
Zhijin Fan

ChemInform ◽  
2010 ◽  
Vol 41 (50) ◽  
pp. no-no
Author(s):  
Hiroyuki Suga ◽  
Tadashi Arikawa ◽  
Kennosuke Itoh ◽  
Yukihisa Okumura ◽  
Akikazu Kakehi ◽  
...  

Synthesis ◽  
2021 ◽  
Author(s):  
Raghuramaiah Mandadapu ◽  
Amol Satish Dehade ◽  
Shrikant Abhiman Shete ◽  
Mark Montgomery ◽  
Vikas Sikervar ◽  
...  

The [3+2] and [3+3] regioselective cycloaddition reactions of azomethine imines with activated cyclopropanes have been developed using two different Lewis acids. Scandium (III) triflate serves as a catalyst for the [3+2] cycloaddition reactions of azomethine imines with cyclopropanes to form tetrahydropyrazolone derivatives and tricyclic tetrahydrofuran derivatives in moderate yields. In complementary to this, novel [3+3] cycloaddition reactions of azomethine imine with activated cyclopropanes have been developed using EtAlCl2 as a Lewis acid to form hexahydropyridazinone derivatives in high regioselectivity.


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