Synthesis and cytotoxic activity of new hexaazadibenzotetracenes derived from trans-1,2-diaminocyclohexane

被引:2
|
作者
Rakhimova, Elena B. [1 ]
Kirsanov, Victor Yu. [1 ]
Kuzmina, Ulyana Sh. [2 ]
Galyautdinov, Ilgiz V. [2 ]
Vakhitova, Yulia V. [2 ]
机构
[1] Russian Acad Sci, Inst Petrochem & Catalysis, Ufa Fed Res Ctr, Ufa 450075, Russia
[2] Russian Acad Sci, Inst Biochem & Genet, Ufa Fed Res Ctr, Ufa 450054, Russia
关键词
catalysis; heterocyclization; trans-1; 2-diaminocyclohexane; anilines; polycyclic compounds; hexaazadibenzotetracenes; cytotoxic activity; ENANTIOSELECTIVE MICHAEL ADDITIONS; 1,3-DICARBONYL COMPOUNDS; ACIDS;
D O I
10.1016/j.mencom.2023.01.035
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A one-pot synthesis of N,N'-disubstituted (3bR*,7aR*,1 0bR*,14aR*)-octadecahydro-1H,8H- 2,3a,7b,9,10a,14b-hexaazadibenzo[fg, op]tetracenes via the catalytic heterocyclization of trans-1,6,7,12-tetraaza-perhydrotetracene with formaldehyde or CH2(NMe2)2 and anilines has been accomplished. Preliminary screening of thus obtained perhydro hexaazadibenzotetracenes for cytotoxic activity has been performed.
引用
收藏
页码:112 / 114
页数:3
相关论文
共 50 条
  • [31] Chiral trans-1,2-diaminocyclohexane derivatives as chiral solvating agents for carboxylic acids
    Periasamy, Mariappan
    Dalai, Manasi
    Padmaja, Meduri
    JOURNAL OF CHEMICAL SCIENCES, 2010, 122 (04): : 561 - 569
  • [32] Characteristics of Gelation by Amides Based on trans-1,2-Diaminocyclohexane: The Importance of Different Substituents
    Nakagawa, Haruka
    Fujiki, Mamoru
    Sato, Takaaki
    Suzuki, Masahiro
    Hanabusa, Kenji
    BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2017, 90 (03) : 312 - 321
  • [33] Chiral trans-1,2-diaminocyclohexane derivatives as chiral solvating agents for carboxylic acids
    Mariappan Periasamy
    Manasi Dalai
    Meduri Padmaja
    Journal of Chemical Sciences, 2010, 122
  • [34] Preparation of trans-1,2-diaminocyclohexane derivatives by lithium perchlorate catalyzed ring opening of aziridines
    de Parrodi, CA
    Vázquez, V
    Quintero, L
    Juaristi, E
    SYNTHETIC COMMUNICATIONS, 2001, 31 (21) : 3295 - 3302
  • [35] VIBRATIONAL CIRCULAR-DICHROISM OF METAL-COMPLEXES CONTAINING TRANS-1,2-DIAMINOCYCLOHEXANE
    MORIMOTO, H
    KINOSHITA, I
    MORI, M
    KYOGOKU, Y
    SUGETA, H
    CHEMISTRY LETTERS, 1989, (01) : 73 - 76
  • [36] Asymmetric Michael addition promoted by (R,R)-trans-1,2-diaminocyclohexane in ionic liquids
    Gallo, V
    Giardina-Papa, D
    Mastrorilli, P
    Nobile, CF
    Suranna, GP
    Wang, YQ
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2005, 690 (15) : 3535 - 3539
  • [37] Preparative resolution of (±)-trans-1,2-diaminocyclohexane by means of preferential crystallization of its citrate monohydrate
    Galland, Arnaud
    Dupray, Valerie
    Lafontaine, Anais
    Berton, Benjamin
    Sanselme, Morgane
    Atmani, Hassan
    Coquerel, Gerard
    TETRAHEDRON-ASYMMETRY, 2010, 21 (18) : 2212 - 2217
  • [38] Erratum to: Chiral trans-1,2-diaminocyclohexane derivatives as chiral solvating agents for carboxylic acids
    MARIAPPAN PERIASAMY
    MANASI DALAI
    MEDURI PADMAJA
    Journal of Chemical Sciences, 2011, 123 : 365 - 365
  • [39] Synthesis, Characterization, and Structure of a Cyano-bridged Two-dimensional CuIICoIII Coordination Polymer Derived from Trans-1,2-diaminocyclohexane as Blocking Ligand
    Nayak, Malabika
    Majumder, Samit
    Lemoine, Pascale
    Mohanta, Sasankasekhar
    JOURNAL OF CHEMICAL CRYSTALLOGRAPHY, 2008, 38 (12) : 937 - 942
  • [40] Synthesis, Characterization, and Structure of a Cyano-bridged Two-dimensional CuIICoIII Coordination Polymer Derived from Trans-1,2-diaminocyclohexane as Blocking Ligand
    Malabika Nayak
    Samit Majumder
    Pascale Lemoine
    Sasankasekhar Mohanta
    Journal of Chemical Crystallography, 2008, 38 : 937 - 942