Highly enantioselective synthesis of polysubstituted tetrahydroquinolines via organocatalytic Michael/Aza-Henry tandem reactions.

Highly enantioselective synthesis of polysubstituted tetrahydroquinolines via organocatalytic Michael/Aza-Henry tandem reactions.
复制标题

DOI:
10.1021/ol103069d
复制
发表时间:
2011-02
期刊:
影响因子:
5.2
通讯作者:
Zhenhua Jia;Yong-Chun Luo;Peng‐Fei Xu
Zhenhua Jia;Yong-Chun Luo;Peng‐Fei Xu
中科院分区:
化学1区
文献类型:
--
作者:
Zhenhua Jia;Yong-Chun Luo;Peng‐Fei Xu

文献摘要

被引文献

相似文献

Highly enantioselective chiral bifunctional thiourea catalyzed asymmetric tandem reactions for synthesis of substituted tetrahydroquinolines are described. Substituted tetrahydroquinolines were given in good yields (up to 98%), high enantioselectivities (up to >99% ee), and diastereoselectivities (up to 20:1 dr).