Oxalic acid as the in situ carbon monoxide generator in palladium-catalyzed hydroxycarbonylation of arylhalides

2017 ◽  
Vol 15 (23) ◽  
pp. 5033-5040 ◽  
Author(s):  
Changdong Shao ◽  
Ailan Lu ◽  
Xiaoling Wang ◽  
Bo Zhou ◽  
Xiaohong Guan ◽  
...  

Oxalic acid as a highly efficient, safe and tractable concentrated carbon monoxide surrogate was successfully introduced into the palladium-catalyzed hydroxycarbonylation of arylhalides.

2020 ◽  
Vol 59 (41) ◽  
pp. 17887-17896 ◽  
Author(s):  
Philip Boehm ◽  
Sven Roediger ◽  
Alessandro Bismuto ◽  
Bill Morandi

1995 ◽  
Vol 50 (3) ◽  
pp. 430-438 ◽  
Author(s):  
Wilhelm Keim ◽  
Heiko Maas ◽  
Stefan Mecking

Cationic palladium catalysts have been used to cooligomerize ethylene and carbon monoxide. At high ethylene/CO ratios (m /m = 10:1) in methylene chloride as a solvent, unsaturated alternating cooligomers of the general structure R[C(O)CH2CH2]mH ( m ≥ 1 ; R ≡CH2=CH-, CH2=CHCH2CH2- and CH3CH = CHCH2-) were obtained for the first time. Single component catalyst precursors [(allyl)Pd(P^X )]+Y- (P^X = Ph2P(CH2)nC(= O )OR, Ph2P(CH2)2P(=O)Ph2, Ph2P(CH2)nPh2P(CH2)2S (=O )Ph, n = 1 - 3 , R = Me, Et; Y- = BF4-, SbF6- ) with bidentate P,O- and P,S-ligands as well as in situ catalysts with unfunctionalized phosphine ligands were used. With P"Bu3 as a ligand, selectivities for ethylvinylketone of 40% based on the CO converted were obtained. The hemilabile phosphino-ester and phosphinothiophene ligands behave like monodentate phosphines under catalytic conditions.


RSC Advances ◽  
2016 ◽  
Vol 6 (82) ◽  
pp. 78468-78476 ◽  
Author(s):  
Abdol-Reza Hajipour ◽  
Zeinab Tavangar-Rizi ◽  
Nasser Iranpoor

Preparation and characterization of palladium nanoparticles immobilized on magnetic methionine-functionalized chitosan as a highly efficient, air stable, and readily reusable heterogeneous catalyst in carbonylation reactions.


Synthesis ◽  
2019 ◽  
Vol 52 (04) ◽  
pp. 581-590 ◽  
Author(s):  
Zhaotao Xu ◽  
Bin Huang ◽  
Zebiao Zhou ◽  
Mingzhong Cai

A highly efficient and practical heterogeneous palladium-catalyzed carbonylative coupling of 2-iodoanilines with aryl iodides has been developed. The reaction occurs smoothly in toluene at 110 °C with N,N-diisopropylethylamine as base under carbon monoxide (5 bar) and offers a general and powerful tool for the construction of various valuable 2-arylbenzoxazinones with excellent atom-economy, high functional group tolerance, good to high yields, and easy recyclability of the palladium catalyst. The reaction is the first example of heterogeneous palladium-catalyzed carbonylative coupling for the preparation of diverse 2-arylbenzoxazinones from commercially easily available 2-iodoanilines and aryl iodides.


2020 ◽  
Vol 132 (41) ◽  
pp. 18043-18052 ◽  
Author(s):  
Philip Boehm ◽  
Sven Roediger ◽  
Alessandro Bismuto ◽  
Bill Morandi

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