Palladium-catalyzed aerobic oxidative carbonylation of alkynes with amines: a general access to substituted maleimides

2018 ◽  
Vol 54 (76) ◽  
pp. 10710-10713 ◽  
Author(s):  
Ji Yang ◽  
Jiawang Liu ◽  
Ralf Jackstell ◽  
Matthias Beller
Keyword(s):  
Oxidative Carbonylation ◽  
Carbonylation Reaction ◽  
Palladium Catalyzed

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

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
Keyword(s):  
Carbon Monoxide ◽  
Oxidative Carbonylation ◽  
Influence Of Temperature ◽  
Carbonylation Reaction ◽  
Palladium Catalyzed ◽  
Effects Of Temperature ◽  
Temperature And Pressure

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.

Palladium-catalyzed oxidative carbonylation of hydrazides: synthesis of 1,3,4-oxadiazol-2(3H)-ones

2015 ◽  
Vol 51 (10) ◽  
pp. 1905-1907 ◽  
Author(s):  
Yu Wang ◽  
Xu Meng ◽  
Yuting Yang ◽  
Lutao Zhang ◽  
Shuaibo Guo ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Carbonyl Group ◽  
Intramolecular Cyclization ◽  
Oxidative Carbonylation ◽  
Amine Group ◽  
Mild Conditions ◽  
Carbonylation Reaction ◽  
Efficient Access ◽  
Wide Range ◽  
Palladium Catalyzed

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.

ChemInform Abstract: Palladium-Catalyzed Oxidative Carbonylation of the Alkenyl C-H Bonds of Enamides: Synthesis of 1,3-Oxazin-6-ones.

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

Palladium-Catalyzed Oxidative Carbonylation ofN-Allylamines for the Synthesis of β-Lactams

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

Pd/C-catalyzed synthesis of oxamates by oxidative cross double carbonylation of alcohols and tertiary amines through C–N bond cleavage

2019 ◽  
Vol 43 (46) ◽  
pp. 18072-18078 ◽  
Author(s):  
Yuvraj A. Kolekar ◽  
Bhalchandra M. Bhanage
Keyword(s):  
Active Compound ◽  
Bond Cleavage ◽  
Tertiary Amines ◽  
Carbonylation Reaction ◽  
Palladium Catalyzed ◽  
Biological Active Compound

Palladium-catalyzed oxidative cross double carbonylation reaction between tertiary amines and alcohols using oxidant O2 and KI as the additive affords oxamates. Oxamate are as a intermediate in biological active compound and glycol synthesis.

Synthesis of indolo- and pyrrolo[1,2-a]quinoxalinones through a palladium-catalyzed oxidative carbonylation of the C2 position of indole

2020 ◽  
Vol 18 (8) ◽  
pp. 1612-1622 ◽  
Author(s):  
Attoor Chandrasekhar ◽  
Sethuraman Sankararaman
Keyword(s):  
Oxidative Carbonylation ◽  
Palladium Catalyzed

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.

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 ◽  
...  
Keyword(s):  
High Efficiency ◽  
Oxidative Carbonylation ◽  
Atom Economy ◽  
Palladium Catalyzed

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.

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