Palladium-catalyzed carbonylation of 1,5-cyclooctadiene. Effects of temperature and pressure

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.

2015 ◽  
Vol 51 (10) ◽  
pp. 1905-1907 ◽  
Author(s):  
Yu Wang ◽  
Xu Meng ◽  
Yuting Yang ◽  
Lutao Zhang ◽  
Shuaibo Guo ◽  
...  

A novel palladium-catalyzed oxidative carbonylation reaction was developed via the carbon monoxide insertions between the amine group and the carbonyl group to realize the intramolecular cyclization, which provides efficient access to 1,3,4-oxadiazol-2(3H)-ones with a wide range of substrates under mild conditions, resulting in good to excellent yields.


2011 ◽  
Vol 2011 ◽  
pp. 1-11 ◽  
Author(s):  
Katarina Novakovic ◽  
Julie Parker

Palladium(II) iodide is used as a catalyst in the phenylacetylene oxidative carbonylation reaction that has demonstrated oscillatory behaviour in both pH and heat of reaction. In an attempt to extract the reaction network responsible for the oscillatory nature of this reaction, the system was divided into smaller parts and they were studied. This paper focuses on understanding the reaction network responsible for the initial reactions of palladium(II) iodide within this oscillatory reaction. The species researched include methanol, palladium(II) iodide, potassium iodide, and carbon monoxide. Several chemical reactions were considered and applied in a modelling study. The study revealed the significant role played by traces of water contained in the standard HPLC grade methanol used.


1992 ◽  
Vol 57 (11) ◽  
pp. 2374-2382 ◽  
Author(s):  
Curtis B. Anderson ◽  
Rade Marković

Oxidative carbonylation of 1,5-cyclooctadiene in methylene chloride-methanol mixture, catalyzed by Pd(II)-salts, gave rise to a bicyclic, bifunctional product under mild experimental conditions. The mechanism, involving multiple carbon monoxide and double bond insertions into the Pd(II)-carbon σ-bond, has been proposed, as being consistent with the outcome of this novel ring closure reaction.


2018 ◽  
Vol 54 (76) ◽  
pp. 10710-10713 ◽  
Author(s):  
Ji Yang ◽  
Jiawang Liu ◽  
Ralf Jackstell ◽  
Matthias Beller

A catalytic oxidative carbonylation reaction was developed for the synthesis of polysubstituted maleimides from alkynes and amines with air as a green oxidant.


2017 ◽  
Vol 19 (23) ◽  
pp. 6432-6435 ◽  
Author(s):  
Jiwei Wu ◽  
Yuchen Zhou ◽  
Ting Wu ◽  
Yi Zhou ◽  
Chien-Wei Chiang ◽  
...  

1990 ◽  
Vol 9 (1) ◽  
pp. 26-30 ◽  
Author(s):  
Philippe Brechot ◽  
Yves Chauvin ◽  
Dominique Commereuc ◽  
Lucien Saussine

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