Magic of Alpha: The Chemistry of a Remarkable Bidentate Phosphine, 1,2-Bis(di-tert-butylphosphinomethyl)benzene

被引:58
作者
Vondran, Johanna [1 ]
Furst, Marc R. L. [2 ,3 ]
Eastham, Graham R. [4 ]
Seidensticker, Thomas [1 ]
Cole-Hamilton, David J. [2 ]
机构
[1] TU Dortmund Univ, Dept Biochem & Chem Engn, Lab Ind Chem, D-44227 Dortmund, Germany
[2] Univ St Andrews, EaStCHEM, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[3] Athenee Luxembourg, L-1430 Luxembourg, Luxembourg
[4] Darlington Co, 30 Thornfield Rd, Durham DL3 9TQ, England
关键词
PALLADIUM-CATALYZED METHOXYCARBONYLATION; PAUSON-KHAND REACTION; CARBON-MONOXIDE; ALTERNATING COPOLYMERIZATION; ISOMERIZING ALKOXYCARBONYLATION; METHYL PROPANOATE; FATTY-ACIDS; ASTERISK-CARBONYLIERUNG; METHANOL CARBONYLATION; UNSATURATED ESTERS;
D O I
10.1021/acs.chemrev.0c01254
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The bidentate phosphine ligand 1,2-bis(di-tert-butylphosphinomethyl)-benzene (1,2-DTBPMB) has been reported over the years as being one of, if not the, best ligands for achieving the alkoxycarbonylation of various unsaturated compounds. Bonded to palladium, the ligand provides the basis for the first step in the commercial (Alpha) production of methyl methacrylate as well as very high selectivity to linear esters and acids from terminal or internal double bonds. The present review is an overview covering the literature dealing with the 1,2-DTBPMB ligand: from its first reference, its catalysis, including the alkoxycarbonylation reaction and its mechanism, its isomerization abilities including the highly selective Isomerizing methoxycarbonylation, other reactions such as cross-coupling, recycling approaches, and the development of improved, modified ligands, in which some tert-butyl ligands are replaced by 2-pyridyl moieties and which show exceptional rates for carbonylation reactions at low temperatures.
引用
收藏
页码:6610 / 6653
页数:44
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