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Highly enantio- and diastereoselective reductive aldol reactions catalyzed by chiral Spiro bisphosphine oxides
Alternative Title手性螺环双膦氧催化的高对映选择性和高非对映选择性的还原Aldol反应
Zhang PK(张攀科); Liu JW(刘家旺); Wang Z(王正); Ding KL(丁奎岭)
2015
Source PublicationChin. J. Catal.
Volume36Issue:1Pages:100-105
AbstractA Spiro bisphosphine oxide (SpinPO) was found to be an efficient chiral Lewis base catalyst in asymmetric reductive aldol reaction of enones and aldehydes in the presence of trichlorosilane as the reductant, affording a variety of beta-hydroxyketones in good yields with moderate to high levels of diastereo- and enantioselectivities. (C) 2015, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
Subtype论文
Subject Area金属有机化学
DOI10.1016/S1872-2067(14)60241-2
URL查看原文
Indexed BySCI
Language英语
WOS IDWOS:000348274200015
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39561
Collection金属有机化学国家重点实验室
Corresponding AuthorDing KL(丁奎岭)
Affiliation中科院上海有机化学研究所, 金属有机化学国家重点实验室
Recommended Citation
GB/T 7714
Zhang PK,Liu JW,Wang Z,et al. Highly enantio- and diastereoselective reductive aldol reactions catalyzed by chiral Spiro bisphosphine oxides[J]. Chin. J. Catal.,2015,36(1):100-105.
APA 张攀科,刘家旺,王正,&丁奎岭.(2015).Highly enantio- and diastereoselective reductive aldol reactions catalyzed by chiral Spiro bisphosphine oxides.Chin. J. Catal.,36(1),100-105.
MLA 张攀科,et al."Highly enantio- and diastereoselective reductive aldol reactions catalyzed by chiral Spiro bisphosphine oxides".Chin. J. Catal. 36.1(2015):100-105.
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