Ruthenium-exchanged FAU-Y zeolite catalyzed improvement in the synthesis of 6H-indolo[2,3-b]quinolines

被引:29
作者
Khorshidi, Alireza [1 ]
Tabatabaeian, Khalil [1 ]
机构
[1] Univ Guilan, Fac Sci, Dept Chem, Rasht, Guilan, Iran
关键词
Ruthenium-exchanged zeolite; 6H-Indolo[2,3-b]quinoline; Catalyst; C=C-CONJUGATED CARBODIIMIDES; TOPOISOMERASE-II INHIBITORS; CRYPTOLEPIS SANGUINOLENTA; ALKALOID CRYPTOTACKIEINE; INDOLE-DERIVATIVES; CYTOTOXIC ACTIVITY; SURFACE-ACIDITY; EFFICIENT ROUTE; MCM-41; NEOCRYPTOLEPINE;
D O I
10.1016/j.molcata.2011.05.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ruthenium-exchanged FAU-Y zeolite (RuY) was used as a recyclable catalyst for preparation of 6H-indolo[2,3-b]quinolines from the reaction of indole-3-carbaldehyde with aryl amines in refluxing dioxane. Under the above mentioned conditions, reasonable yields of the desired products with different substituents on the quinoline ring were obtained. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:128 / 131
页数:4
相关论文
共 30 条
  • [1] Formal total synthesis of the alkaloid cryptotackieine (neocryptolepine)
    Alajarin, M
    Molina, P
    Vidal, A
    [J]. JOURNAL OF NATURAL PRODUCTS, 1997, 60 (07): : 747 - 748
  • [2] New synthesis of benzo-δ-carbolines, cryptolepines, and their salts:: In vitro cytotoxic, antiplasmodial, and antitrypanosomal activities of δ-caribolines, benzo-δ-carbolines, and cryptolepines
    Arzel, E
    Rocca, P
    Grellier, P
    Labaeïd, M
    Frappier, F
    Guéritte, F
    Gaspard, C
    Marsais, F
    Godard, A
    Quéguiner, G
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (06) : 949 - 960
  • [3] The design and synthesis of novel 3-[2-indol-1-yl-ethyl]-1-H-indole derivatives as selective inhibitors of CDK4
    Aubry, C
    Patel, A
    Mahale, S
    Chaudhuri, B
    Maréchal, JD
    Suteliffe, MJ
    Jenkins, PR
    [J]. TETRAHEDRON LETTERS, 2005, 46 (09) : 1423 - 1425
  • [4] FLUORIDE AND SULFATE TREATMENT OF ALPO4-AL2O3 CATALYSTS .1. STRUCTURE, TEXTURE, SURFACE-ACIDITY AND CATALYTIC PERFORMANCE IN CYCLOHEXENE CONVERSION AND CUMENE CRACKING
    BAUTISTA, FM
    CAMPELO, JM
    GARCIA, A
    LUNA, D
    MARINAS, JM
    ROMERO, AA
    NAVIO, JA
    MACIAS, M
    [J]. JOURNAL OF CATALYSIS, 1994, 145 (01) : 107 - 125
  • [5] Surface acidity of MCM-41 by in situ IR studies of pyridine adsorption
    Chakraborty, B
    Viswanathan, B
    [J]. CATALYSIS TODAY, 1999, 49 (1-3) : 253 - 260
  • [6] STUDIES ON ORDERED MESOPOROUS MATERIALS .3. COMPARISON OF MCM-41 TO MESOPOROUS MATERIALS DERIVED FROM KANEMITE
    CHEN, CY
    XIAO, SQ
    DAVIS, ME
    [J]. MICROPOROUS MATERIALS, 1995, 4 (01): : 1 - 20
  • [7] Synthesis and cytotoxic activity evaluation of indolo-, pyrrolo-, and benzofuro-quinolin-2(1H)-ones and 6-anilinoindoloquinoline derivatives
    Chen, YL
    Chung, CH
    Chen, IL
    Chen, PH
    Jeng, HY
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2002, 10 (08) : 2705 - 2712
  • [8] New alkaloids from Cryptolepis sanguinolenta
    Cimanga, K
    DeBruyne, T
    Pieters, L
    Claeys, M
    Vlietinck, A
    [J]. TETRAHEDRON LETTERS, 1996, 37 (10) : 1703 - 1706
  • [9] Antibacterial and antifungal activities of neocryptolepine, biscryptolepine and cryptoquindoline, alkaloids isolated from Cryptolepis sanguinolenta
    Cimanga, K
    De Bruyne, T
    Pieters, L
    Totte, J
    Tona, L
    Kambu, K
    Vanden Berghe, D
    Vlietinck, AJ
    [J]. PHYTOMEDICINE, 1998, 5 (03) : 209 - 214
  • [10] In vitro biological activities of alkaloids from Cryptolepis sanguinolenta
    Cimanga, K
    DeBruyne, T
    Lasure, A
    VanPoel, B
    Pieters, L
    Claeys, M
    VandenBerghe, D
    Kambu, K
    Tona, L
    Vlietinck, AJ
    [J]. PLANTA MEDICA, 1996, 62 (01) : 22 - 27