Chiral N-heterocyclic carbene ligands derived from 2,2′-bipiperidine and partially reduced biisoquinoline:: Rhodium and iridium complexes in asymmetric catalysis

被引:100
作者
Herrmann, Wolfgang A. [1 ]
Baskakov, Denys
Herdtweck, Eberhardt
Hoffmann, Stephan D.
Bunlaksananusorn, Tanasri
Rampf, Florian
Rodefeld, Lars
机构
[1] Tech Univ Munich, Lehrstuhl Anorgan Chem, D-85747 Garching, Germany
[2] Tech Univ Munich, Lehrstuhl Anorgan Chem Schwerpunkt Neue Mat, D-85747 Garching, Germany
[3] Lanxess Deutschland GmbH, BU Fine Chem, Process Dev, D-51369 Leverkusen, Germany
关键词
D O I
10.1021/om060098b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
New and reliable procedures for the preparation of both enantiomers of 2,2'-bipiperidine have been developed. Chiral imidazolinium salts derived from 2,2'-bipiperidine and partially reduced biisoquinoline were prepared in high yields. Rhodium and iridium complexes of new chiral N-heterocyclic carbenes were obtained by transmetalation from corresponding silver(I) complexes. The structures of these complexes were verified by X-ray diffraction. The novel carbenes seem to range between the very electron-rich bis(amido)carbenes and the imidazole-derived carbenes with regard to the electronic ligand properties (IR evidence). Rhodium and iridium complexes were applied to a variety of catalytic asymmetric reactions. Modest enantioselectivities of up to 28% ee were observed.
引用
收藏
页码:2449 / 2456
页数:8
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