Chiral Phosphoric Acid Catalyzed Atroposelective C-H Amination of Arenes

被引:156
作者
Xia, Wang [1 ,2 ]
An, Qian-Jin [1 ,2 ]
Xiang, Shao-Hua [1 ,2 ,3 ]
Li, Shaoyu [1 ,2 ,3 ]
Wang, Yong-Bin [1 ,2 ]
Tan, Bin [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen 518055, Peoples R China
[2] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China
[3] Southern Univ Sci & Technol, Acad Adv Interdisciplinary Studies, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
amination; atropisomerism; chiral phosphoric acid; heterocycles; organocatalysis; FRIEDEL-CRAFTS ALKYLATION; CROSS-COUPLING REACTIONS; MANNICH-TYPE REACTION; N BOND FORMATION; ENANTIOSELECTIVE SYNTHESIS; BIARYL ATROPISOMERS; NATURAL-PRODUCTS; BRONSTED ACID; COPPER; CONSTRUCTION;
D O I
10.1002/anie.202000585
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
N-arylcarbazole structures are important because of their prevalence in natural products and functional OLED materials. C-H amination of arenes has been widely recognized as the most efficient approach to access these structures. Conventional strategies involving transition-metal catalysts suffer from confined substrate generality and the requirement of exogenous oxidants. Organocatalytic enantioselective C-N chiral axis construction remains elusive. Presented here is the first organocatalytic strategy for the synthesis of novel axially chiral N-arylcarbazole frameworks by the assembly of azonaphthalenes and carbazoles. This reaction accommodates broad substrate scope and gives atropisomeric N-arylcarbazoles in good yields with excellent enantiocontrol. This approach not only offers an alternative to metal-catalyzed C-N cross-coupling, but also brings about opportunities for the exploitation of structurally diverse N-aryl atropisomers and OLED materials.
引用
收藏
页码:6775 / 6779
页数:5
相关论文
共 88 条
  • [1] Enantioselective Mannich-type reaction catalyzed by a chiral Bronsted acid
    Akiyama, T
    Itoh, J
    Yokota, K
    Fuchibe, K
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (12) : 1566 - 1568
  • [2] [Anonymous], 2019, Angew. Chem, V131, P6780
  • [3] [Anonymous], 2004, ANGEW CHEM-GER EDIT
  • [4] [Anonymous], 2008, Amino Group Chemistry: from Synthesis to the Life Sciences
  • [5] [Anonymous], 2004, ANGEW CHEM INT EDIT
  • [6] New catalytic approaches in the stereoselective Friedel-Crafts alkylation reaction
    Bandini, M
    Melloni, A
    Umani-Ronchi, A
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (05) : 550 - 556
  • [7] Bandini M., 2009, ANGEW CHEM, V121, P9786
  • [8] Catalytic Functionalization of Indoles in a New Dimension
    Bandini, Marco
    Eichholzer, Astrid
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (51) : 9608 - 9644
  • [9] Bidirectional enantioselective synthesis of bis-benzofuran atropisomeric oligoarenes featuring two distal C-C stereogenic axes
    Bao, Xiaoze
    Rodriguez, Jean
    Bonne, Damien
    [J]. CHEMICAL SCIENCE, 2020, 11 (02) : 403 - 408
  • [10] C-N bond forming cross-coupling reactions: an overview
    Bariwal, Jitender
    Van der Eycken, Erik
    [J]. CHEMICAL SOCIETY REVIEWS, 2013, 42 (24) : 9283 - 9303