Palladium-Catalyzed CC Bond Formation To Construct 1,4-Diketones under Mild Conditions

2011 ◽  
Vol 123 (32) ◽  
pp. 7475-7479 ◽  
Author(s):  
Chao Liu ◽  
Yi Deng ◽  
Jing Wang ◽  
Yingying Yang ◽  
Shan Tang ◽  
...  
2011 ◽  
Vol 50 (32) ◽  
pp. 7337-7341 ◽  
Author(s):  
Chao Liu ◽  
Yi Deng ◽  
Jing Wang ◽  
Yingying Yang ◽  
Shan Tang ◽  
...  

ChemInform ◽  
2011 ◽  
Vol 42 (52) ◽  
pp. no-no
Author(s):  
Chao Liu ◽  
Yi Deng ◽  
Jing Wang ◽  
Yingying Yang ◽  
Shan Tang ◽  
...  

2021 ◽  
Author(s):  
K. R. Holman ◽  
A. M. Stanko ◽  
S. E. Reisman

This tutorial review highlights the use of palladium-catalyzed cascade cyclizations in natural product synthesis, focusing on cascades that construct multiple rings and form both C–C and C–X (X = O, N) bonds in a single synthetic operation.


2020 ◽  
Vol 02 (03) ◽  
pp. e128-e132
Author(s):  
Shao-Zheng Guo ◽  
Zhi-Qun Yu ◽  
Wei-Ke Su

AbstractThe development of highly efficient C–C bond formation methods for the synthesis of ethyl 2-(2,4-dichloro-5-fluorobenzoyl)-3-(dimethylamino)acrylate 1 in continuous flow processes has been described, which is based on the concept of rapid and efficient activation of carboxylic acid. 2,4-Dichloro-5-fluorobenzoic acid is rapidly converted into highly reactive 2,4-dichloro-5-fluorobenzoyl chloride by treating with inexpensive and less-toxic solid bis(trichloromethyl)carbonate. And then it rapidly reacts with ethyl 3-(dimethylamino)acrylate to afford the desired 1. This process can be performed under mild conditions. Compared with the traditional tank reactor process, less raw material consumption, higher product yield, less reaction time, higher operation safety ensured by more the environmentally friendly procedure, and process continuity are achieved in the continuous-flow system.


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