Your browser doesn't support javascript.
loading
Magic of Alpha: The Chemistry of a Remarkable Bidentate Phosphine, 1,2-Bis(di-tert-butylphosphinomethyl)benzene.
Vondran, Johanna; Furst, Marc R L; Eastham, Graham R; Seidensticker, Thomas; Cole-Hamilton, David J.
Affiliation
  • Vondran J; Laboratory for Industrial Chemistry, Department of Biochemical and Chemical Engineering, TU Dortmund University, Emil-Figge-Straße 66, 44227 Dortmund, Germany.
  • Furst MRL; EaStCHEM, School of Chemistry, University of St Andrews, St Andrews, KY16 9ST Scotland, U.K.
  • Eastham GR; Athénée du Luxembourg, 24, Boulevard Pierre Dupong, L-1430 Luxembourg, Luxembourg.
  • Seidensticker T; 30 Thornfield Road, Darlington, Co., Durham DL3 9TQ, U.K.
  • Cole-Hamilton DJ; Laboratory for Industrial Chemistry, Department of Biochemical and Chemical Engineering, TU Dortmund University, Emil-Figge-Straße 66, 44227 Dortmund, Germany.
Chem Rev ; 121(11): 6610-6653, 2021 06 09.
Article in En | MEDLINE | ID: mdl-33961414
ABSTRACT
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.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Rev Year: 2021 Type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Rev Year: 2021 Type: Article Affiliation country: Germany