期刊
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
卷 307, 期 1-2, 页码 149-153出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.molcata.2009.03.019
关键词
Thiophene ligands; Asymmetric transfer hydrogenation; Aromatic ketone; Chiral alcohols
资金
- National Natural Science Foundation of China [20423002, 20703034]
- Natural Science Foundation of Fujian Province of China [2008J0235]
- State Key Laboratory of Physical Chemistry of Solid Surfaces in Xiamen University
The chiral diamino-bis(bithiophene) ligands were firstly employed in the irridium(I)-catalyzed asymmetric transfer hydrogenation of aromatic ketones. The new catalyst systems, generated in situ from chiral diamino-bis(bithiophene) ligands and IrCl(CO)(PPh3)(2) in (PrOH)-Pr-i, gave the corresponding optically active secondary alcohols with high yield and fair to good enantioselectivities (up to 90% ee). The chiral Ir(I)/diamino-bis(bithiophene) complexes were also synthesized and characterized. The XPS spectra showed that the potentially multidentate ligands coordinated to the It atom through the nitrogen atoms, while the thiophene pendants did not participate in coordination to the It atom. (C) 2009 Elsevier B.V. All rights reserved.
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