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首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >Synthesis of a chiral pyridylphosphine ligand and a comparison of its rhodium complex with the structurally similar arylphosphine rhodium catalysts in the asymmetric hydrogenation of 2-(6 '-methoxy-2 '-naphthyl)propenoic acid
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Synthesis of a chiral pyridylphosphine ligand and a comparison of its rhodium complex with the structurally similar arylphosphine rhodium catalysts in the asymmetric hydrogenation of 2-(6 '-methoxy-2 '-naphthyl)propenoic acid

机译:手性吡啶基膦配体的合成及其铑配合物与结构相似的芳基膦铑催化剂在2-(6'-甲氧基-2'-萘基)丙烯酸不对称氢化中的比较

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摘要

A chiral pyridylphosphine ligand (2R,4R)-2,4-bis[di-3'-(2',6'-dimethoxypyridyl)phosphino]pentane was synthesized. The rhodium catalyzed asymmetric hydrogenation of 2-(6'-methoxy-2'-naphthyl)propenoic acid was studied by using this ligand in comparison with the structurally similar Skewphos analogs. (C) 1998 Elsevier Science Ltd. All rights reserved. [References: 9]
机译:合成了手性吡啶基膦配体(2R,4R)-2,4-双[di-3′-(2′,6′-二甲氧基吡啶基)膦基]戊烷。与结构相似的Skewphos类似物相比,使用该配体研究了铑催化的2-(6'-甲氧基-2'-萘基)丙烯酸的不对称氢化。 (C)1998 Elsevier ScienceLtd。保留所有权利。 [参考:9]

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