Catalytic Asymmetric Cascade Vinylogous Mukaiyama 1,6-Michael/Michael Addition of 2-Silyloxyfurans with Azoalkenes: Direct Approach to Fused Butyrolactones

被引:89
作者
Li, Jun [1 ]
Huang, Rong [1 ]
Xing, Yi-Kang [1 ]
Qiu, Guofu [2 ]
Tao, Hai-Yan [1 ]
Wang, Chun-Jiang [1 ,3 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Sch Pharmaceut Sci, Wuhan 430072, Peoples R China
[3] Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
关键词
PHOSPHINE-OXAZOLINE LIGANDS; ENANTIOSELECTIVE SYNTHESIS; MANNICH REACTIONS; ALDOL REACTION; 1,3-DIPOLAR CYCLOADDITION; MICHAEL REACTION; HETEROCYCLES; BUTENOLIDES; DERIVATIVES; EFFICIENT;
D O I
10.1021/jacs.5b06509
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An unprecedented cascade vinylogous Mukaiyama 1,6-MA/MA of 2-silyloxyfurans and azoalkenes was realized with a Cu(II)/Bu-t-Box complex. An array of fused butyrolactones containing multiple stereocenters was generally obtained in good yield (up to 90% yield) with exclusive diastereoselectivity (>20:1 dr) and excellent enantioselectivity (up to 99% ee). Carbon isotope effects measured by C-13 NMR revealed a stepwise mechanism for this annulation process.
引用
收藏
页码:10124 / 10127
页数:4
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