Palladium-catalyzed C3-selective C–H oxidative carbonylation of imidazo[1,2-a]pyridines with CO and alcohols: a way to access esters

2020 ◽  
Vol 7 (4) ◽  
pp. 697-701 ◽  
Author(s):  
Shoucai Wang ◽  
Siyu Zhang ◽  
Meichen Liu ◽  
Jiawang Zang ◽  
Guangbin Jiang ◽  
...  

A palladium-catalyzed C3-selective C–H oxidative carbonylation for the synthesis of various esters from imidazo[1,2-a]pyridines and CO with high efficiency and high atom economy has been developed.

1991 ◽  
Vol 56 (3) ◽  
pp. 663-672 ◽  
Author(s):  
Curtis B. Anderson ◽  
Rade Marković

The influence of temperature and carbon monoxide pressure on the course of oxidative carbonylation reaction of 1,5-cyclooctadiene in the presence of the palladium(II) salts as a catalyst, was investigated.


ChemInform ◽  
2014 ◽  
Vol 45 (20) ◽  
pp. no-no
Author(s):  
Ming Chen ◽  
Zhi-Hui Ren ◽  
Yao-Yu Wang ◽  
Zheng-Hui Guan

2014 ◽  
Vol 53 (9) ◽  
pp. 2443-2446 ◽  
Author(s):  
Wu Li ◽  
Chao Liu ◽  
Heng Zhang ◽  
Keyin Ye ◽  
Guanghui Zhang ◽  
...  

2020 ◽  
Vol 18 (8) ◽  
pp. 1612-1622 ◽  
Author(s):  
Attoor Chandrasekhar ◽  
Sethuraman Sankararaman

A methodology that involves the Pd-catalyzed direct C(sp2)–H bond carbonylation of the C2 position of indole has been introduced for the synthesis of indolo[1,2-a]quinoxalin-6(5H)-ones.


2011 ◽  
Vol 282 (1) ◽  
pp. 120-127 ◽  
Author(s):  
Nicola Della Ca’ ◽  
Paolo Bottarelli ◽  
Angela Dibenedetto ◽  
Michele Aresta ◽  
Bartolo Gabriele ◽  
...  

2017 ◽  
Vol 13 ◽  
pp. 2610-2616 ◽  
Author(s):  
Tao Fan ◽  
Wei-Dong Meng ◽  
Xingang Zhang

An efficient palladium-catalyzed Heck-type reaction of secondary trifluoromethylated alkyl bromides has been developed. The reaction proceeds under mild reaction conditions with high efficiency and excellent functional group tolerance, even towards formyl and hydroxy groups. Preliminary mechanistic studies reveal that a secondary trifluoromethylated alkyl radical is involved in the reaction.


Sign in / Sign up

Export Citation Format

Share Document