A Catalyst-Free Synthesis of Fused Perfluoroalkylated 2,3-Dihydroisoxazoles via Oxa-Michael-Aldol Annulation

Synthesis ◽  
2021 ◽  
Author(s):  
Wei Zhou ◽  
Lan Yao ◽  
Hui Zhang ◽  
Xiaojun Tang ◽  
Weiguo Cao ◽  
...  

AbstractA novel synthesis of fused perfluoroalkylated 2,3-dihydroisoxazoles is achieved via oxa-Michael-aldol annulation between perfluoroalk-2-ynoates and N-hydroxyimides. This method provides a convenient route for the synthesis of pyrrolidin-2-one-fused perfluoroalkylated 2,3-dihydroisoxazoles in yields of up to 97%. Diverse and pharmaceutically attractive polycyclic scaffolds can be obtained rapidly and efficiently under these mild, catalyst-free conditions.

2014 ◽  
Vol 25 (10) ◽  
pp. 1395-1398 ◽  
Author(s):  
Li-Cai Zhao ◽  
Zhi-Qiang Hou ◽  
Chun-Ze Liu ◽  
Yuan-Yuan Wang ◽  
Li-Yi Dai

RSC Advances ◽  
2013 ◽  
Vol 3 (39) ◽  
pp. 18049 ◽  
Author(s):  
Prasad Yadav ◽  
Chetan Chanmal ◽  
Aniruddha Basu ◽  
Lily Mandal ◽  
Jyoti Jog ◽  
...  

2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  

A metal- and catalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a SET event involving a photoexcited electron-donor-aceptor complex between NHPI ester and Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. <a>The method provides an operationally simple, robust and step-economical approach to the construction of diversely functionalized dihydroquinolinones bearing quaternary-centers. A sequential one-pot hydroalkylation-isomerization approach is also allowed giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance was observed in both approaches</a>.


2000 ◽  
Author(s):  
Thorsten Schroer ◽  
Karl O. Christe
Keyword(s):  

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