Direct, highly enantioselective pyrrolidine sulfonamide catalyzed Michael addition reactions of aldehydes and ketones to nitrostyrenes and applications for formal synthesis of montanine alkaloids.

被引：0
|
作者：
Wang, W [1 ]
Wang, J [1 ]
Li, H [1 ]
机构：
[1] Univ New Mexico, Dept Chem, Albuquerque, NM 87131 USA
来源：
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2005年 / 229卷
关键词：
D O I：
暂无
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
356-ORGN
引用
收藏
页码：U382 / U382
页数：1
相关论文
共 23 条
  • [21] One-step, efficient synthesis of combined threonine-surfactant organocatalysts for the highly enantioselective direct aldol reactions of cyclic ketones with aromatic aldehydes in the presence of water
    Wu, Chuanlong
    Fu, Xiangkai
    Ma, Xuebing
    Li, Shi
    TETRAHEDRON-ASYMMETRY, 2010, 21 (20) : 2465 - 2470
  • [22] ORGN 145-Direct, pyrrolidine sulfonamide-promoted enantioselective aldol reactions of alpha, alpha-dialkyl-aldehydes: Synthesis of quaternary carbon-containing beta-hydroxy carbonyl compounds
    Li, Hao
    Wang, Jian
    Wang, Wei
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2006, 232
  • [23] Highly enantioselective synthesis of chiral 3,4-dihydro-2H-pyran-5-carbonitrile via tandem Michael addition/asymmetric transfer hydrogenation/cyclization reactions catalyzed by a bifunctional NoyoriIkariya type catalyst
    Zheng, Dongsong
    Liu, Rui
    Wang, Yu
    Cheng, Tanyu
    Liu, Guohua
    MOLECULAR CATALYSIS, 2018, 455 : 103 - 107
123