中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Chiral sulfoxide-olefin ligands: tunable stereoselectivity in Rh-catalyzed asymmetric 1,4-additions

文献类型:期刊论文

作者Chen, Guihua ; Gui, Jiangyang ; Cao, Peng ; Liao, Jian
刊名TETRAHEDRON
出版日期2012
卷号68期号:15页码:3220-3224
关键词Sulfoxide-olefin 1 Rh-catalyzed 4-Addition Stereoselectivity reversal
ISSN号0040-4020
产权排序2
通讯作者Liao, J (reprint author), Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China.
英文摘要A class of chiral sulfoxide-olefins were designed and synthesized through concise routes. Their applications as ligands in Hayashi-Miyaura reaction were studied, which found that vinyl substituents of the ligands vary in stereocontrolling ability. Particularly, either isomer of adducts with excellent ees could be readily obtained through changing the position of the substituents of olefins as well as changing the configuration of the C=C bond of the ligands. Meanwhile, the substrate scope of arylboronic acids and alkenes was clearly shown. (C) 2012 Elsevier Ltd. All rights reserved.
学科主题Chemistry
收录类别SCI
资助信息NSFC [21072186, 20872139]; West Light Foundation of CAS; Chengdu Institute of Biology of CAS [Y0B1051100]; Major State Basic Research Development Program (973 program) [2010CB833300]
语种英语
WOS记录号WOS:000302593200011
公开日期2013-07-03
源URL[http://210.75.237.14/handle/351003/23901]  
专题成都生物研究所_天然产物研究
推荐引用方式
GB/T 7714
Chen, Guihua,Gui, Jiangyang,Cao, Peng,et al. Chiral sulfoxide-olefin ligands: tunable stereoselectivity in Rh-catalyzed asymmetric 1,4-additions[J]. TETRAHEDRON,2012,68(15):3220-3224.
APA Chen, Guihua,Gui, Jiangyang,Cao, Peng,&Liao, Jian.(2012).Chiral sulfoxide-olefin ligands: tunable stereoselectivity in Rh-catalyzed asymmetric 1,4-additions.TETRAHEDRON,68(15),3220-3224.
MLA Chen, Guihua,et al."Chiral sulfoxide-olefin ligands: tunable stereoselectivity in Rh-catalyzed asymmetric 1,4-additions".TETRAHEDRON 68.15(2012):3220-3224.

入库方式: OAI收割

来源:成都生物研究所

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