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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 >Asymmetric synthesis. Part 29: Asymmetric hydroformylation of styrene catalyzed by chiral spiro diphosphite-rhodium(I) complexes
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Asymmetric synthesis. Part 29: Asymmetric hydroformylation of styrene catalyzed by chiral spiro diphosphite-rhodium(I) complexes

机译:不对称合成。第29部分:手性螺二亚磷酸酯-铑(I)配合物催化的苯乙烯不对称加氢甲酰化

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Chiral diphosphite ligands L-1-L-3 were prepared by the reaction of (1S,5S,6R)-(cis,trans)-spiro[4.4]nonane-1,6-diol with chlorophosphites. These ligands were tested in the rhodium catalyzed hydroformylation of styrene and enantioselectivities up to 69% were achieved. High regioselectivities (97%) to 2-phenylpropanal and high yields (98%) were obtained under mild reaction conditions. The influence of reaction conditions is also discussed. (C) 1998 Elsevier Science Ltd. All rights reserved. [References: 11]
机译:通过(1S,5S,6R)-(顺式,反式)-螺[4.4]壬烷-1,6-二醇与氯代亚磷酸酯的反应制备手性二亚磷酸酯配体L-1-L-3。在铑催化的苯乙烯的加氢甲酰化反应中测试了这些配体,对映选择性高达69%。在温和的反应条件下,对2-苯基丙醛的区域选择性高(97%),产率高(98%)。还讨论了反应条件的影响。 (C)1998 Elsevier ScienceLtd。保留所有权利。 [参考:11]

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