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Catalytic asymmetric [2,3] sigmatropic rearrangement of sulfur ylides generated from carbenoids and propargyl sulfides
Zhang, XM ; Ma, M ; Wang, JB
刊名tetrahedron asymmetry
2003
关键词< < DIAZO-COMPOUNDS ALLYL SULFIDES MECHANISM ESTERS 2,3> 2,3> -SIGMATROPIC REARRANGEMENT SIGMATROPIC REARRANGEMENT
DOI10.1016/S0957-4166(03)00018-1
英文摘要Catalytic asymmetric [2,3] sigmatropic rearrangement of sulfur ylides generated from aryldiazoacetates and propargyl sulfides with a number of chiral Rh(II) and Cu(1) catalysts have been investigated and moderately high enantioselectivities (up to 81% ee) have been achieved. (C) 2003 Elsevier Science Ltd. All rights reserved.; Chemistry, Inorganic & Nuclear; Chemistry, Organic; Chemistry, Physical; SCI(E); 29; ARTICLE; 7; 891-895; 14
语种英语
内容类型期刊论文
源URL[http://ir.pku.edu.cn/handle/20.500.11897/255985]  
专题化学与分子工程学院
推荐引用方式
GB/T 7714
Zhang, XM,Ma, M,Wang, JB. Catalytic asymmetric [2,3] sigmatropic rearrangement of sulfur ylides generated from carbenoids and propargyl sulfides[J]. tetrahedron asymmetry,2003.
APA Zhang, XM,Ma, M,&Wang, JB.(2003).Catalytic asymmetric [2,3] sigmatropic rearrangement of sulfur ylides generated from carbenoids and propargyl sulfides.tetrahedron asymmetry.
MLA Zhang, XM,et al."Catalytic asymmetric [2,3] sigmatropic rearrangement of sulfur ylides generated from carbenoids and propargyl sulfides".tetrahedron asymmetry (2003).
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