메뉴 건너뛰기




Volumn 2, Issue 2, 2010, Pages

A simple and convenient method for the synthesis of perimidine derivatives catalyzed by nano-silica sulfuric acid

Author keywords

1,8 diaminonaphthalene; Aromatic aldehydes; Nano silica sulfuric acid; Perimidine

Indexed keywords


EID: 79958706983     PISSN: 19430876     EISSN: 19430884     Source Type: Journal    
DOI: 10.1080/19430876.2010.532429     Document Type: Article
Times cited : (15)

References (19)
  • 1
    • 84944052334 scopus 로고    scopus 로고
    • Perimidines and Their Benzo Derivatives
    • In, Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon: Oxford
    • Undheim, K.; Benneche, T. Perimidines and Their Benzo Derivatives. In Comprehensive Heterocyclic Chemistry, Vol. 6; Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon: Oxford, 1996, pp. 93-231.
    • (1996) Comprehensive Heterocyclic Chemistry , vol.6 , pp. 93-231
    • Undheim, K.1    Benneche, T.2
  • 2
    • 0035821604 scopus 로고    scopus 로고
    • Synthesis and cytotoxic activity of 7-oxo-7Hdibenz[f, ij]isoquinoline and 7-oxo-7H-benzo[e]perimidine derivatives
    • Bu, X.; Deady, L. W.; Finlay, G. J.; Baguley, B. C.; Denny, W.A. Synthesis and cytotoxic activity of 7-oxo-7Hdibenz[f, ij]isoquinoline and 7-oxo-7H-benzo[e]perimidine derivatives. J. Med. Chem. 2001, 44, 2004-2014.
    • (2001) J. Med. Chem. , vol.44 , pp. 2004-2014
    • Bu, X.1    Deady, L.W.2    Finlay, G.J.3    Baguley, B.C.4    Denny, W.A.5
  • 4
    • 0023553457 scopus 로고
    • Potential antitumor agents. 53. Synthesis, DNA binding properties, and biological activity of perimidines designed as "minimal" DNA-intercalating agents
    • Herbert, J. M.; Woodgate, P. D.; Denny, W. A. Potential antitumor agents. 53. Synthesis, DNA binding properties, and biological activity of perimidines designed as "minimal" DNA-intercalating agents. J. Med. Chem. 1987, 30, 2081-2086.
    • (1987) J. Med. Chem. , vol.30 , pp. 2081-2086
    • Herbert, J.M.1    Woodgate, P.D.2    Denny, W.A.3
  • 5
    • 34250408056 scopus 로고
    • Synthesis of 2-(5-halogeno-2-furyl)-2,3-dihydroperimidines
    • Starshikov, N. M.; Pozharskii, F. T. Synthesis of 2-(5-halogeno-2-furyl)-2,3-dihydroperimidines. Chem. Heterocycl. Comp. 1975, 9, 922-924.
    • (1975) Chem. Heterocycl. Comp. , vol.9 , pp. 922-924
    • Starshikov, N.M.1    Pozharskii, F.T.2
  • 6
    • 70349647016 scopus 로고    scopus 로고
    • Zeolite catalyzed efficient synthesis of perimidines at room temperature
    • Mobinikhaledi, A.; Foroughifar, N.; Basaki, N. Zeolite catalyzed efficient synthesis of perimidines at room temperature. Turk. J. Chem. 2009, 33, 555-560.
    • (2009) Turk. J. Chem. , vol.33 , pp. 555-560
    • Mobinikhaledi, A.1    Foroughifar, N.2    Basaki, N.3
  • 7
    • 67651240594 scopus 로고    scopus 로고
    • Synthesis of perimidines using copper nitrate as an efficient catalyst
    • Mobinikhaledi, A.; Steel. P. J. Synthesis of perimidines using copper nitrate as an efficient catalyst. Synth. React. Inorg. Met. Org. Chem. 2009, 39, 133-135.
    • (2009) Synth. React. Inorg. Met. Org. Chem. , vol.39 , pp. 133-135
    • Mobinikhaledi, A.1    Steel, P.J.2
  • 8
    • 34548291489 scopus 로고    scopus 로고
    • Ruthenium (III) chloride as an efficient catalyst for the synthesis of perimidine derivatives under mild conditions
    • Zhang, J.; Zhang, S. L.; Zhang, J. M. Ruthenium (III) chloride as an efficient catalyst for the synthesis of perimidine derivatives under mild conditions. Chin. Chem. Lett. 2007, 18, 1057-1060.
    • (2007) Chin. Chem. Lett. , vol.18 , pp. 1057-1060
    • Zhang, J.1    Zhang, S.L.2    Zhang, J.M.3
  • 9
    • 0037136395 scopus 로고    scopus 로고
    • Vinylphosphonium salt mediated simple synthesis of 7-oxo-7H-pyrido[1,2,3-cd]perimidine derivatives. Dynamic NMR spectroscopic study of prototropic tautomerism in ethyl 1H-perimidine-2-carboxylate
    • Yavari, I.; Adib, M.; Jahani-Moghaddam, F.; Bijanzadeh, H. R. Vinylphosphonium salt mediated simple synthesis of 7-oxo-7H-pyrido[1,2,3-cd]perimidine derivatives. Dynamic NMR spectroscopic study of prototropic tautomerism in ethyl 1H-perimidine-2-carboxylate. Tetrahedron, 2002, 58, 6901-6906.
    • (2002) Tetrahedron , vol.58 , pp. 6901-6906
    • Yavari, I.1    Adib, M.2    Jahani-Moghaddam, F.3    Bijanzadeh, H.R.4
  • 12
    • 0033530917 scopus 로고    scopus 로고
    • Heterogeneous catalytic transformations for environmentally friendly production
    • Sheldon, R. A.; Downing, R. S. Heterogeneous catalytic transformations for environmentally friendly production. Appl. Catal. A 1999, 189, 163-183.
    • (1999) Appl. Catal. A , vol.189 , pp. 163-183
    • Sheldon, R.A.1    Downing, R.S.2
  • 13
    • 27744511324 scopus 로고    scopus 로고
    • New heterogeneous process for biodiesel production: A way to improve the quality and the value of the crude glycerin produced by biodiesel plants
    • Bournay, L.; Casanave, D.; Delfort, B.; Hillion, G.; Chodorge, J. A. New heterogeneous process for biodiesel production: A way to improve the quality and the value of the crude glycerin produced by biodiesel plants. Catal. Today 2005, 106, 190-192.
    • (2005) Catal. Today , vol.106 , pp. 190-192
    • Bournay, L.1    Casanave, D.2    Delfort, B.3    Hillion, G.4    Chodorge, J.A.5
  • 14
    • 42049084169 scopus 로고    scopus 로고
    • A novel efficient four-and five-component, one-pot synthesis of 4-semicarbazonoalkyl-2-naphthols
    • Foroughifar, N., Mobinikhaledi, A., Moghanian, H., Ebrahimi, S., and Bodaghi Farad, M. A. A novel efficient four-and five-component, one-pot synthesis of 4-semicarbazonoalkyl-2-naphthols. Synlett 2008, 821-826.
    • (2008) Synlett , pp. 821-826
    • Foroughifar, N.1    Mobinikhaledi, A.2    Moghanian, H.3    Ebrahimi, S.4    Bodaghi Farad, M.A.5
  • 15
    • 70349219888 scopus 로고    scopus 로고
    • Simple and efficient method for synthesis of novel 4-substituted 1-acylthiosemicarbazides via one-pot multicomponent reactions
    • Foroughifar, N., Mobinikhaledi, A., andMoghanian, H. Simple and efficient method for synthesis of novel 4-substituted 1-acylthiosemicarbazides via one-pot multicomponent reactions. Synthetic Comm. 2009, 39, 3668-3676.
    • (2009) Synthetic Comm. , vol.39 , pp. 3668-3676
    • Foroughifar, N.1    Mobinikhaledi, A.2    Moghanian, H.3
  • 16
    • 77249131230 scopus 로고    scopus 로고
    • A straightforward and efficient catalyst-free one-pot synthesis of n-acyl-1,3-diaryl-2-azaphenalene derivatives via multicomponent reactions
    • Foroughifar, N., Mobinikhaledi, A., and Moghanian, H. A straightforward and efficient catalyst-free one-pot synthesis of n-acyl-1,3-diaryl-2-azaphenalene derivatives via multicomponent reactions. Chem. Lett., 2010, 39, 180-181.
    • (2010) Chem. Lett. , vol.39 , pp. 180-181
    • Foroughifar, N.1    Mobinikhaledi, A.2    Moghanian, H.3
  • 17
    • 77951224178 scopus 로고    scopus 로고
    • A catalytic and green procedure for synthesis of 12-arylor 12-alkyl-8,9,10,12-tetrahydrobenzo[α]xanthen-11-one derivatives under solvent-free conditions
    • Foroughifar, N.; Mobinikhaledi, A.; Moghanian, H. A. A catalytic and green procedure for synthesis of 12-arylor 12-alkyl-8,9,10,12-tetrahydrobenzo[α]xanthen-11-one derivatives under solvent-free conditions. International Journal of Green Nanotechnology: Physics & Chemistry 2009, 1, 57-63.
    • (2009) International Journal of Green Nanotechnology: Physics & Chemistry , vol.1 , pp. 57-63
    • Foroughifar, N.1    Mobinikhaledi, A.2    Moghanian, H.A.3
  • 18
    • 0012459240 scopus 로고    scopus 로고
    • 2 as a novel heterogeneous system for the nitration of phenols under mild conditions
    • 2 as a novel heterogeneous system for the nitration of phenols under mild conditions. Molecules 2002, 7, 734-742.
    • (2002) Molecules , vol.7 , pp. 734-742
    • Zolfigol, M.A.1    Madrakian, E.2    Ghaemi, E.3
  • 19
    • 0035851246 scopus 로고    scopus 로고
    • 2 as a novel heterogeneous system for production of thionitriles and disulfides under mild conditions
    • 2 as a novel heterogeneous system for production of thionitriles and disulfides under mild conditions. Tetrahedron 2001, 57, 9509-9511.
    • (2001) Tetrahedron , vol.57 , pp. 9509-9511
    • Zolfigol, M.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.