中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly enantio- and diastereoselective reductive aldol reactions catalyzed by chiral Spiro bisphosphine oxides

文献类型:期刊论文

作者Zhang PK(张攀科); Liu JW(刘家旺); Wang Z(王正); Ding KL(丁奎岭)
刊名Chin. J. Catal.
出版日期2015
卷号36期号:1页码:100-105
其他题名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
通讯作者丁奎岭
英文摘要A 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.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1016/S1872-2067(14)60241-2
语种英语
WOS记录号WOS:000348274200015
源URL[http://ir.sioc.ac.cn/handle/331003/39561]  
专题上海有机化学研究所_金属有机化学国家重点实验室
作者单位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
推荐引用方式
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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来源:上海有机化学研究所

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