中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Palladium-catalyzed asymmetric allylic substitutions by axially chiral P,S-, S,S-, and S,O-heterodonor ligands with a binaphthalene framework

文献类型:期刊论文

作者Shi M(施敏) ; Zhang W(张雯)
刊名Tetrahedron-Asymmetry
出版日期2004
卷号15期号:19页码:3161-3169
其他题名Palladium-Catalyzed Asymmetric Allylic Substitutions by Axially Chiral P,S-; S,S-; and S,O-Heterodonor Ligands with Binaphthalene Framework.
通讯作者施敏
英文摘要Axially chiral P,S-heterodonor ligand L1 is effective in the asymmetric allylic substitution of 1,3-diphenylpropenyl acetate with dimethyl malonate. its bidentate coordination pattern to a I'd metal center with both P and S atoms has been unambiguously established by X-ray diffraction and NMR spectroscopic analyses. Herein, we further disclose that axially chiral S,S-heterodonor ligands L2-L4 are also effective in the same reaction to give the allylic alkylation product in moderate to good ee. However, the corresponding S,O-heterodonor ligands are not as effective as the corresponding P,S- or S,S-heterodonor ligands in the same asymmetric reaction. (C) 2004 Elsevier Ltd. 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/j.tetasy.2004.08.008
语种英语
WOS记录号WOS:000224447500020
公开日期2013-01-09
源URL[http://202.127.28.38/handle/331003/9940]  
专题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
Shi M,Zhang W. Palladium-catalyzed asymmetric allylic substitutions by axially chiral P,S-, S,S-, and S,O-heterodonor ligands with a binaphthalene framework[J]. Tetrahedron-Asymmetry,2004,15(19):3161-3169.
APA Shi M,&Zhang W.(2004).Palladium-catalyzed asymmetric allylic substitutions by axially chiral P,S-, S,S-, and S,O-heterodonor ligands with a binaphthalene framework.Tetrahedron-Asymmetry,15(19),3161-3169.
MLA Shi M,et al."Palladium-catalyzed asymmetric allylic substitutions by axially chiral P,S-, S,S-, and S,O-heterodonor ligands with a binaphthalene framework".Tetrahedron-Asymmetry 15.19(2004):3161-3169.

入库方式: OAI收割

来源:上海有机化学研究所

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