Hafnium Triflate as an Efficient Catalyst for Direct Friedel-Crafts Reactions of Chromene Hemiacetals

被引:36
|
作者
Wu, Yan-Chao [1 ]
Li, Hui-Jing [1 ]
Liu, Li [1 ]
Demoulin, Nicolas [2 ]
Liu, Zhe [1 ]
Wang, Dong [1 ]
Chen, Yong-Jun [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, BNLMS, CAS Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
[2] CNRS, Inst Chim Subst Nat, F-91198 Gif Sur Yvette, France
基金
中国国家自然科学基金;
关键词
chromenes; Friedel-Crafts reaction; hafnium; hemiacetals; selectivity; ELECTRON-RICH ARENES; ASYMMETRIC-SYNTHESIS; ALLYLIC ALKYLATION; ENANTIOSELECTIVE SYNTHESIS; MULTICOMPONENT APPROACH; SALICYLIC ALDEHYDES; FACILE SYNTHESIS; ALCOHOLS; GLYCOSYLATION; AMINOMETHYLATION;
D O I
10.1002/adsc.201000930
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The direct Friedel-Crafts reaction of chromene hemiacetals with indoles, furans and sterically hindered anilines has been accomplished with high selectivity and excellent yields in the presence of a catalytic amount of hafnium triflate [Hf(OTf)(4), 0.1 mol%, 0-40 degrees C]. The mild conditions tolerate various sensitive functional and protecting groups, and the products were confirmed unambiguously from their spectra and by single-crystal X-ray analysis. This direct Friedel-Crafts reaction of chromene hemiacetals should inspire and encourage the consideration of hafnium triflate in the development of mild reaction conditions for the efficient derivatization of hemiacetal-containing compounds.
引用
收藏
页码:907 / 912
页数:6
相关论文
共 50 条
  • [41] Quaternary Phosphonium Salts as Active Bronsted Acid Catalysts for Friedel-Crafts Reactions
    Chen, Lin
    Xiao, Ben-Xian
    Du, Wei
    Chen, Ying-Chun
    ORGANIC LETTERS, 2019, 21 (14) : 5733 - 5736
  • [42] Enantioselective Friedel-Crafts Alkylation Reactions of β-Naphthols with Donor-Acceptor Aminocyclopropanes
    Zhu, Man
    Wang, Dong-Chao
    Xie, Ming-Sheng
    Qu, Gui-Rong
    Guo, Hai-Ming
    CHEMISTRY-A EUROPEAN JOURNAL, 2018, 24 (58) : 15512 - 15516
  • [43] Br2 as a novel Lewis acid catalyst for Friedel-Crafts alkylation of indoles with α,β-unsaturated ketones
    Liang, Deqiang
    Li, Xiangguang
    Zhang, Wanshun
    Li, Yanni
    Zhang, Mi
    Cheng, Ping
    TETRAHEDRON LETTERS, 2016, 57 (09) : 1027 - 1030
  • [44] Indium triflate: An efficient catalyst for acylation reactions
    Chauhan, KK
    Frost, CG
    Love, I
    Waite, D
    SYNLETT, 1999, (11) : 1743 - 1744
  • [45] An Efficient Enantioselective Method for Asymmetric Friedel-Crafts Alkylation of Indoles with α,β-Unsaturated Aldehydes
    Hong, Liang
    Wang, Lei
    Chen, Chao
    Zhang, Bangzhi
    Wang, Rui
    ADVANCED SYNTHESIS & CATALYSIS, 2009, 351 (05) : 772 - 778
  • [46] Catalytic Friedel-Crafts acylation: magnetic nanopowder CuFe2O4 as an efficient and magnetically separable catalyst
    Parella, Ramarao
    Naveen
    Kumar, Amit
    Babu, Srinivasarao Arulananda
    TETRAHEDRON LETTERS, 2013, 54 (13) : 1738 - 1742
  • [47] Highly efficient asymmetric organocatalytic Friedel-Crafts alkylation of indoles with α,β-unsaturated aldehydes
    Jin, Shangbin
    Li, Chenguang
    Ma, Yuanhui
    Kan, Yuhe
    Zhang, Yong Jian
    Zhang, Wanbin
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2010, 8 (17) : 4011 - 4015
  • [48] A chiral multidentate salan-supported heterobimetallic catalyst for asymmetric Friedel-Crafts reaction
    Xiong, Hangxing
    Li, Li
    Liu, E.
    Cheng, Jessica
    Zhang, Guoqi
    INORGANIC CHEMISTRY COMMUNICATIONS, 2017, 84 : 24 - 27
  • [49] Enantioselective organocatalytic Friedel-Crafts reaction of electron-rich phenols and isatins by Takemoto's thiourea catalyst
    Chen, Zhe
    Wang, Liming
    Tian, Wenqin
    Jin, Ying
    Qin, Xin
    MOLECULAR DIVERSITY, 2024, 28 (03) : 1733 - 1742
  • [50] Halogen Bond-Catalyzed Friedel-Crafts Reactions of Furans Using a 2,2'-Bipyridine-Based Catalyst
    Zhang, Huimiao
    Toy, Patrick H.
    ADVANCED SYNTHESIS & CATALYSIS, 2021, 363 (01) : 215 - 221