Highly Enantioselective Assembly of Functionalized Tetrahydroquinolines with Creation of an All-Carbon Quaternary Center

被引:41
|
作者
Tan, Hao Rui [1 ]
Ng, Hui Fen [1 ]
Chang, Jun [2 ]
Wang, Jian [1 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] Fudan Univ, Sch Pharm, Shanghai 201203, Peoples R China
关键词
asymmetric synthesis; cascade reactions; organocatalysis; tetrahydroquinolines; thioureas; CATALYTIC ASYMMETRIC-SYNTHESIS; MICHAEL ADDITION; TRANSFER HYDROGENATION; CONJUGATE ADDITION; ORGANIC-SYNTHESIS; ACID; QUINOLINES; DERIVATIVES; ALKALOIDS; LIGANDS;
D O I
10.1002/chem.201103136
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
引用
收藏
页码:3865 / 3870
页数:6
相关论文
共 50 条
  • [1] Organocatalytic enantioselective domino synthesis of highly functionalized cyclohexanes with an all-carbon quaternary stereocenter
    Zhao, Gui-Ling
    Dziedzic, Pawel
    Ullah, Farman
    Eriksson, Lars
    Cordova, Armando
    TETRAHEDRON LETTERS, 2009, 50 (26) : 3458 - 3462
  • [2] Efficient and highly enantioselective formation of the all-carbon quaternary stereocentre of lyngbyatoxin A
    Vital, Paulo
    Tanner, David
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2006, 4 (23) : 4292 - 4298
  • [3] Pd-Catalyzed Enantioselective Creation of All-Carbon Quaternary Center with 2,3-Allenylic Carbonates
    Lin, Jie
    Jia, Minqiang
    Song, Xu
    Yu, Hao
    Ma, Shengming
    ORGANIC LETTERS, 2024, 26 (12) : 2349 - 2353
  • [4] 'On water' organocatalyzed enantioselective synthesis of highly functionalized cyclohexanones with an all-carbon quaternary centre from allylidene malononitriles and enones
    Vamisetti, Ganga B.
    Chowdhury, Raghunath
    Kumar, Mukesh
    Ghosh, Sunil K.
    TETRAHEDRON-ASYMMETRY, 2017, 28 (02) : 317 - 323
  • [5] Catalytic enantioselective construction of all-carbon quaternary stereocenters
    Trost, BM
    Jiang, CH
    SYNTHESIS-STUTTGART, 2006, (03): : 369 - 396
  • [6] Enantioselective Assembly of Cycloenones with a Nitrile-Containing All-Carbon Quaternary Center from Malononitriles Enabled by Ni Catalysis
    Lu, Zhiwu
    Hu, Xu-Dong
    Zhang, Hui
    Zhang, Xiao-Wen
    Cai, Jinhui
    Usman, Muhammad
    Cong, Hengjiang
    Liu, Wen-Bo
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (16) : 7328 - 7333
  • [7] Enantioselective Cyclopropanation of Indoles: Construction of All-Carbon Quaternary Stereocenters
    Oezueduru, Guelsuem
    Schubach, Thea
    Boysen, Mike M. K.
    ORGANIC LETTERS, 2012, 14 (19) : 4990 - 4993
  • [8] Enantioselective β-alkylation of pyrroles with the formation of an all-carbon quaternary stereocenter
    Ma, Qiao
    Gong, Lei
    Meggers, Eric
    ORGANIC CHEMISTRY FRONTIERS, 2016, 3 (10): : 1319 - 1325
  • [9] Highly enantioselective hydrovinylation of α-alkyl vinylarenes. An approach to the construction of all-carbon quaternary stereocenters
    Shi, Wen-Jian
    Zhang, Qi
    Xie, Jian-Hua
    Zhu, Shou-Fei
    Hou, Guo-Hua
    Zhou, Qi-Lin
    Journal of the American Chemical Society, 2006, 128 (09): : 2780 - 2781
  • [10] Enantioselective synthesis of a substituted cyclopentanone with all-carbon quaternary stereocenter
    Lozanova, Antonina V.
    Stepanov, Andrei V.
    Zlokazov, Mikhail V.
    Veselovsky, Vladimir V.
    ARKIVOC, 2017, : 217 - 224