4.7 Article

Highly enantioselective iridium-catalyzed hydrogenation of quinoline derivatives using chiral phosphinite H8-BINAPO

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ADVANCED SYNTHESIS & CATALYSIS
卷 347, 期 14, 页码 1755-1758

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200505130

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asymmetric hydrogenation; immobilization; iridium; phosphinite ligands; poly(ethylene glycol) dimethyl ether; quinoline

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The chiral diphosphinite H8-BINAPO derived from H8-BINOL has been used in the Ir-catalyzed asymmetric hydrogenation of quinolines, and high enantioselectivity (up to 97% ee) was obtained. Immobilization of the iridium catalyst in poly(ethylene glycol) dimethyl ether (DMPEG) is also discussed. With DMPEG/hexane biphasic system, better enantioselectivities were obtained as compared to those observed in aprotic organic solvents.

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