中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enatioselective organocatalytic synthesis of highly functionalized tetrahydrothiophenes by a michael-aldol cascade reaction (vol 50, pg 2946, 2009)

文献类型:期刊论文

作者Luo, Guangshun1; Zhang, Shilei1; Duan, Wenhu1,2; Wang, Wei1,2,3
刊名Tetrahedron letters
出版日期2010-05-12
卷号51期号:19页码:2667-2667
ISSN号0040-4039
DOI10.1016/j.tetlet.2010.03.056
通讯作者Duan, wenhu(wduan@mail.shcnc.ac.cn)
WOS研究方向Chemistry
WOS类目Chemistry, Organic
语种英语
WOS记录号WOS:000277696000028
出版者PERGAMON-ELSEVIER SCIENCE LTD
URI标识http://www.irgrid.ac.cn/handle/1471x/2414876
专题中国科学院大学
通讯作者Duan, Wenhu
作者单位1.E China Univ Sci & Technol, Sch Pharm, Dept Pharmaceut, Shanghai 200237, Peoples R China
2.Chinese Acad Sci, Grad Sch, Shanghai Inst Biol Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
3.Univ New Mexico, Dept Chem & Chem Biol, Albuquerque, NM 87131 USA
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GB/T 7714
Luo, Guangshun,Zhang, Shilei,Duan, Wenhu,et al. Enatioselective organocatalytic synthesis of highly functionalized tetrahydrothiophenes by a michael-aldol cascade reaction (vol 50, pg 2946, 2009)[J]. Tetrahedron letters,2010,51(19):2667-2667.
APA Luo, Guangshun,Zhang, Shilei,Duan, Wenhu,&Wang, Wei.(2010).Enatioselective organocatalytic synthesis of highly functionalized tetrahydrothiophenes by a michael-aldol cascade reaction (vol 50, pg 2946, 2009).Tetrahedron letters,51(19),2667-2667.
MLA Luo, Guangshun,et al."Enatioselective organocatalytic synthesis of highly functionalized tetrahydrothiophenes by a michael-aldol cascade reaction (vol 50, pg 2946, 2009)".Tetrahedron letters 51.19(2010):2667-2667.

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来源:中国科学院大学

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