Unexpected Formation of the Novel Fluorinated Diazenes.

ChemInform ◽  
2004 ◽  
Vol 35 (10) ◽  
Author(s):  
Shizheng Zhu ◽  
Guifang Jin ◽  
Ping He ◽  
Yong Xu ◽  
Qichen Huang
2017 ◽  
Vol 15 (30) ◽  
pp. 6447-6450 ◽  
Author(s):  
F. I. Zubkov ◽  
E. A. Kvyatkovskaya ◽  
E. V. Nikitina ◽  
P. N.-A. Amoyaw ◽  
V. V. Kouznetsov ◽  
...  

It has been proved that the reaction between furfuryl amines and N-R-maleimides leads to the formation of aza-Michael addition products – 3-(furylmethylamino)-N-R-pyrrolidine-2,5-diones, instead of 7-oxa-2-azabicyclo[2.2.1]hept-5-enes, as this journal reported previously.


2001 ◽  
Vol 627 (1) ◽  
pp. 67-70 ◽  
Author(s):  
Philippe Schollhammer ◽  
François Y Pétillon* ◽  
Jean Talarmin ◽  
Kenneth W Muir*

2002 ◽  
Vol 21 (17) ◽  
pp. 3675-3677 ◽  
Author(s):  
Liang-Fu Tang ◽  
Jian-Fang Chai ◽  
Zhi-Hong Wang ◽  
Wen-Li Jia ◽  
Ji-Tao Wang

2003 ◽  
Vol 44 (48) ◽  
pp. 8717-8719 ◽  
Author(s):  
Shizheng Zhu ◽  
Guifang Jin ◽  
Ping He ◽  
Yong Xu ◽  
Qichen Huang

2013 ◽  
Vol 11 (3) ◽  
pp. 407-411 ◽  
Author(s):  
Carlos E. Puerto Galvis ◽  
Vladimir V. Kouznetsov

An unexpected intramolecular cyclization during the reaction of furfurylamine with maleimides is reported as a novel strategy for the efficient green synthesis of the 7-oxa-2-azabicyclo[2.2.1]hept-5-ene skeleton.


2010 ◽  
Vol 34 (8) ◽  
pp. S33-S33
Author(s):  
Wenchao Ou ◽  
Haifeng Chen ◽  
Yun Zhong ◽  
Benrong Liu ◽  
Keji Chen

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