Protonated (S)-prolinamide derivatives-water compatible organocatalysts for direct asymmetric aldol reaction

被引:74
|
作者
Chimni, Swapandeep Singh [1 ]
Singh, Sarbjit [1 ]
Mahajan, Dinesh [1 ]
机构
[1] Guru Nanak Dev Univ, Dept Chem, Amritsar 143005, Punjab, India
关键词
D O I
10.1016/j.tetasy.2008.09.020
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Protonated chiral (S)-prolinamide derivatives have been developed as water compatible highly efficient organocatalysts for a direct enantioselective aldol reaction. A simple protonated (S)-prolinamide organocatalyst prepared from L-proline and 3-nitroaniline catalyzes the aldol reaction of unmodified ketones and a variety of aromatic aldehydes yielding aldol product in high yield with enantioselectivities of up to 98% and diastereoselectivity of up to >99:1. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2276 / 2284
页数:9
相关论文
共 50 条
  • [1] Recyclable silica-supported prolinamide organocatalysts for direct asymmetric Aldol reaction in water
    Monge-Marcet, Amalia
    Cattoen, Xavier
    Alonso, Diego A.
    Najera, Carmen
    Man, Michel Wong Chi
    Pleixats, Roser
    GREEN CHEMISTRY, 2012, 14 (06) : 1601 - 1610
  • [2] Protonated chiral prolinamide catalyzed enantioselective direct aldol reaction in water
    Chimni, SS
    Mahajan, D
    Babu, VVS
    TETRAHEDRON LETTERS, 2005, 46 (34) : 5617 - 5619
  • [3] Novel prolinamide-ureas as organocatalysts for the asymmetric aldol reaction
    Revelou, Panagiota
    Kokotos, Christoforos G.
    Moutevelis-Minakakis, Panagiota
    TETRAHEDRON, 2012, 68 (42) : 8732 - 8738
  • [4] Ion-Tagged Prolinamide Organocatalysts for the Direct Aldol Reaction On-Water
    Eyckens, Daniel J.
    Brozinski, Hannah L.
    Delaney, Joshua P.
    Servinis, Linden
    Naghashian, Sahar
    Henderson, Luke C.
    CATALYSIS LETTERS, 2016, 146 (01) : 212 - 219
  • [5] Ion-Tagged Prolinamide Organocatalysts for the Direct Aldol Reaction On-Water
    Daniel J. Eyckens
    Hannah L. Brozinski
    Joshua P. Delaney
    Linden Servinis
    Sahar Naghashian
    Luke C. Henderson
    Catalysis Letters, 2016, 146 : 212 - 219
  • [6] Multifunctional phosphoramide-(S)-prolinamide derivatives as efficient organocatalysts in asymmetric aldol and Michael reactions
    Cruz-Hernandez, Carlos
    Landeros, Jose M.
    Juaristi, Eusebio
    NEW JOURNAL OF CHEMISTRY, 2019, 43 (14) : 5455 - 5465
  • [7] L-Prolinamide derivatives as efficient organocatalysts for aldol reactions on water
    Tang, Gongkun
    Hu, Xianming
    Altenbach, Hans Josef
    TETRAHEDRON LETTERS, 2011, 52 (52) : 7034 - 7037
  • [8] Design, Synthesis and Organocatalysis of 2,2′-Biphenol-Based Prolinamide Organocatalysts in the Asymmetric Direct Aldol Reaction in Water
    Zhao, Hong-Wu
    Sheng, Zhi-Hui
    Meng, Wei
    Yue, Yuan-Yuan
    Li, Hai-Long
    Song, Xiu-Qing
    Yang, Zhao
    SYNLETT, 2013, 24 (20) : 2743 - 2747
  • [9] Direct asymmetric aldol reaction catalyzed by simple prolinamide phenols
    Fu, Yu-Qin
    Li, Zai-Chun
    Ding, Ll-Na
    Tao, Jing-Chao
    Zhang, Sheng-Hong
    Tang, Ming-Sheng
    TETRAHEDRON-ASYMMETRY, 2006, 17 (24) : 3351 - 3357
  • [10] Novel poly(2-oxazoline)s with pendant L-prolinamide moieties as efficient organocatalysts for direct asymmetric aldol reaction
    Wang, Yao
    Shen, Huifang
    Zhou, Le
    Hu, Fangyu
    Xie, Shoulei
    Jiang, Liming
    CATALYSIS SCIENCE & TECHNOLOGY, 2016, 6 (17) : 6739 - 6749