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Organocatalytic enantioselective Michael addition of cyclic hemiacetals to nitroolefins: a facile access to chiral substituted 5-and 6-membered cyclic ethers 期刊论文

编号：

1f5fa67b-b6bc-45b6-8af2-48059dbfee94
作者：

Zhu, Yadong^[1,2];Qian, Pengfei^[1,2];Yang, Jiyang^[1,2];Chen, Shaohua^[1,2];Hu, Yanwei^[1,2];Wu, Ping^[3];Wang, Wei^[4];Zhang, Wei(张伟)^[3]Zhang, Shilei^[1,2];
语种：

English
期刊：

ORGANIC & BIOMOLECULAR CHEMISTRY ISSN：1477-0520 2015 年 13 卷 16 期 (4769 - 4775)
收录：
摘要：

An efficient aminocatalytic enantioselective Michael addition of readily available cyclic hemiacetals to nitroolefins has been developed. The strategy serves as a powerful approach to synthetically valuable chiral 3-substituted tetrahydrofurans (THFs) and tetrahydropyrans (THPs). The synthetic utilities of the versatile Michael adducts also have been demonstrated in the synthesis of 2,3-disubstituted cyclic ethers, a-substituted lactones and venlafaxine analogues.
推荐引用方式
GB/T 7714：

Zhu Yadong,Qian Pengfei,Yang Jiyang, et al. Organocatalytic enantioselective Michael addition of cyclic hemiacetals to nitroolefins: a facile access to chiral substituted 5-and 6-membered cyclic ethers [J].ORGANIC & BIOMOLECULAR CHEMISTRY,2015,13(16):4769-4775.
APA：

Zhu Yadong,Qian Pengfei,Yang Jiyang,Chen Shaohua,&Zhang Shilei.(2015).Organocatalytic enantioselective Michael addition of cyclic hemiacetals to nitroolefins: a facile access to chiral substituted 5-and 6-membered cyclic ethers .ORGANIC & BIOMOLECULAR CHEMISTRY,13(16):4769-4775.
MLA：

Zhu Yadong, et al. "Organocatalytic enantioselective Michael addition of cyclic hemiacetals to nitroolefins: a facile access to chiral substituted 5-and 6-membered cyclic ethers" .ORGANIC & BIOMOLECULAR CHEMISTRY 13,16(2015):4769-4775.

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