Rare earth metal oxazoline complexes in asymmetric catalysis

被引:53
|
作者
Ward, Benjamin D. [1 ]
Gade, Lutz H. [2 ]
机构
[1] Cardiff Univ, Sch Chem, Cardiff CF10 3AT, S Glam, Wales
[2] Heidelberg Univ, Inst Anorgan Chem, D-69120 Heidelberg, Germany
关键词
FRIEDEL-CRAFTS ALKYLATIONS; DIELS-ALDER REACTIONS; CHIRAL LEWIS-ACIDS; LANTHANIDE COMPLEXES; EFFICIENT CATALYST; ENANTIOSELECTIVE SYNTHESIS; 1,3-DIPOLAR CYCLOADDITION; POLYMERIZATION CATALYSIS; BIS(OXAZOLINE) LIGANDS; COORDINATION CHEMISTRY;
D O I
10.1039/c2cc34997c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polydentate oxazolines have been employed as highly effective stereodirecting ligands for asymmetric catalysis with metals from across most of the periodic table. Despite their highly versatile coordination chemistry, the use of these ligands tends to be polarised towards late transition metals; their use with early transition metals and the f-elements is significantly less developed. This current article aims to review the coordination chemistry and catalytic applications of Group 3 and lanthanide complexes supported by ligands possessing oxazoline moieties. Oxazoline-containing ligands were first employed in molecular lanthanide catalysis as early as 1997, yet there is still a significant void in the chemical literature in this respect. The ligands generally employed include bis(oxazolinyl)methane ("BOX"), 2,6-bis(oxazolinyl)pyridine ("pybox"), 1,1,1-tris(oxazolinyl)ethane ("trisox"), and others. The complexes are employed in a wide-range of catalytic applications, especially in Lewis acid catalysis, but also in the stereospecific polymerisation of olefins.
引用
收藏
页码:10587 / 10599
页数:13
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