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Volumn 38, Issue 20, 2008, Pages 3530-3542

Efficient NaOH-catalyzed reaction of aromatic aldehyde, cyclic ketones, and malononitrile under solvent-free conditions using a grinding method

Author keywords

2,6 Dicyanoanilines; Green chemistry; Grinding; Solvent free; Synthesis

Indexed keywords

2 AMINO 4 (2 CHLOROPHENYL) 5,6,7,8 TETRAHYDRONAPHTHALENE 1,3 DICARBONITRILE; 2 AMINO 4 (2,4 DICHLOROPHENYL) 5,6,7,8 TETRAHYDRONAPHTHALENE 1,3 DICARBONITRILE; 2 AMINO 4 (3,4 DICHLOROPHENYL) 5,6,7,8 TETRAHYDRONAPHTHALENE 1,3 DICARBONITRILE; 2 AMINO 4 (3,4 DIMETHOXYPHENYL) 5,6,7,8 TETRAHYDRONAPHTHALENE 1,3 DICARBONITRILE; 2 AMINO 4 (3,4 DIMETHYLPHENYL) 5,6,7,8 TETRAHYDRONAPHTHALENE 1,3 DICARBONITRILE; 2 AMINO 4 (4 FLUOROPHENYL) 5,6,7,8 TETRAHYDRONAPHTHALENE 1,3 DICARBONITRILE; 2 AMINO 4 (4 METHOXYPHENYL) 5,6,7,8 TETRAHYDRONAPHTHALENE 1,3 DICARBONITRILE; 2 AMINO 5,6,7,8 TETRAHYDRO 4 4 TOLYLNAPHTHALENE 1,3 DICARBONITRILE; 5 AMINO 2,3 DIHYDRO 7 (4 METHOXYPHENYL) 1H INDENE 4,6 DICARBONITRILE; 5 AMINO 2,3 DIHYDRO 7 4 TOLYL 1H INDENE 4,6 DICARBONITRILE; 5 AMINO 7 (2 CHLOROPHENYL) 2,3 DIHYDRO 1H INDENE 4,6 DICARBONITRILE; 5 AMINO 7 (2,4 DICHLOROPHENYL) 2,3 DIHYDRO 1H INDENE 4,6 DICARBONITRILE; 5 AMINO 7 (3 CHLOROPHENYL) 2,3 DIHYDRO 1H INDENE 4,6 DICARBONITRILE; 5 AMINO 7 (3,4 DICHLOROPHENYL) 2,3 DIHYDRO 1H INDENE 4,6 DICARBONITRILE; 5 AMINO 7 (3,4 DIMETHYLPHENYL) 2,3 DIHYDRO 1H INDENE 4,6 DICARBONITRILE; 5 AMINO 7 (4 CHLOROPHENYL) 2,3 DIHYDRO 1H INDENE 4,6 DICARBONITRILE; ALDEHYDE; ANILINE DERIVATIVE; CYCLOPENTANONE DERIVATIVE; KETONE DERIVATIVE; MALONONITRILE; SODIUM HYDROXIDE; UNCLASSIFIED DRUG;

EID: 53149095826     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910802164724     Document Type: Article
Times cited : (28)

References (19)
  • 1
    • 0000884192 scopus 로고    scopus 로고
    • Solvent-free organic synthesis
    • (a) Tanaka, K.; Toda, F. Solvent-free organic synthesis. Chem. Rev. 2000, 100, 1025-1074;
    • (2000) Chem. Rev , vol.100 , pp. 1025-1074
    • Tanaka, K.1    Toda, F.2
  • 2
    • 33847264465 scopus 로고    scopus 로고
    • A green solventless protocol for Michael addition of phthalimide and saccharin to acrylic acid esters in the presence of zinc oxide as a heterogeneous and reusable catalyst1
    • (b) Shirini, F.; Marjani, K.; Nahzomi, H. T. A green solventless protocol for Michael addition of phthalimide and saccharin to acrylic acid esters in the presence of zinc oxide as a heterogeneous and reusable catalyst1. Arkivoc 2007, 1, 51-57;
    • (2007) Arkivoc , vol.1 , pp. 51-57
    • Shirini, F.1    Marjani, K.2    Nahzomi, H.T.3
  • 3
    • 33746425218 scopus 로고    scopus 로고
    • Synthesis of some 4-bromo-1-naphthyl chalcones using silica-sulfuric acid reagent under solvent free conditions
    • (c) Thirunarayanan, G.; Vanangamudi, G. Synthesis of some 4-bromo-1-naphthyl chalcones using silica-sulfuric acid reagent under solvent free conditions. Arkivoc 2006, 12, 58-64.
    • (2006) Arkivoc , vol.12 , pp. 58-64
    • Thirunarayanan, G.1    Vanangamudi, G.2
  • 4
    • 0034700212 scopus 로고    scopus 로고
    • Toward benign syntheses of pyridines involving sequential solvent free aldol and Michael addition reactions
    • Cave, G. W. V.; Raston, C. L. Toward benign syntheses of pyridines involving sequential solvent free aldol and Michael addition reactions. Chem. Commun. 2000, 2199-2200.
    • (2000) Chem. Commun , pp. 2199-2200
    • Cave, G.W.V.1    Raston, C.L.2
  • 5
    • 0000731628 scopus 로고    scopus 로고
    • Two-directional photoinduced electron transfer in a trichromophoric system
    • Depaemelaere, S.; De Schryver, F. C.; Verhoeven, J. W. Two-directional photoinduced electron transfer in a trichromophoric system. J. Phys. Chem. A 1998, 102, 2109-2116.
    • (1998) J. Phys. Chem. A , vol.102 , pp. 2109-2116
    • Depaemelaere, S.1    De Schryver, F.C.2    Verhoeven, J.W.3
  • 6
    • 0037421075 scopus 로고    scopus 로고
    • Calcite and fluorite as catalyst for the Knövenagel condensation of malononitrile and methyl cyanoacetate under solvent-free conditions
    • Shinobu, W.; Hitomi, S. Calcite and fluorite as catalyst for the Knövenagel condensation of malononitrile and methyl cyanoacetate under solvent-free conditions. Tertahedron Lett. 2003, 44, 399-401.
    • (2003) Tertahedron Lett , vol.44 , pp. 399-401
    • Shinobu, W.1    Hitomi, S.2
  • 7
    • 0001608454 scopus 로고    scopus 로고
    • Sepiol, J.; Milart, P. Elimination of the nitrile group from o-aminonitriles, IV: A new and efficient synthesis of 3,5-diarylaminobenzenes from arylidenemalono-dinitriles and 1- arylethylidenemalonodinitriles. Tetrahedron 1985, 41, 5261-5265.
    • Sepiol, J.; Milart, P. Elimination of the nitrile group from o-aminonitriles, IV: A new and efficient synthesis of 3,5-diarylaminobenzenes from arylidenemalono-dinitriles and 1- arylethylidenemalonodinitriles. Tetrahedron 1985, 41, 5261-5265.
  • 8
    • 0004186505 scopus 로고
    • Fox, M. A, Chanon, M, Eds, Elsevier: Amsterdam
    • Fox, M. A.; Chanon, M. (Eds.) Photoinduced Electron Transfer; Elsevier: Amsterdam, 1988.
    • (1988) Photoinduced Electron Transfer
  • 9
    • 0029124427 scopus 로고
    • Model reactions for photosynthesis - Photoinduced charge and energy transfer between covalently linked porphyrin and quinone units
    • Kurreck, H.; Huber, M. Model reactions for photosynthesis - Photoinduced charge and energy transfer between covalently linked porphyrin and quinone units. Angew. Chem., Int. Ed. Engl. 1995, 34, 849-866.
    • (1995) Angew. Chem., Int. Ed. Engl , vol.34 , pp. 849-866
    • Kurreck, H.1    Huber, M.2
  • 11
    • 0003535541 scopus 로고
    • Petty, M. C, Bryce, M. R, Bloor, D, Eds, Oxford University Press: New York
    • Petty, M. C.; Bryce, M. R.; Bloor, D. (Eds.). Introduction to Molecular Electronics; Oxford University Press: New York, 1995.
    • (1995) Introduction to Molecular Electronics
  • 12
    • 0025880703 scopus 로고
    • The reaction of malononitrile with chalcone: A controversial chemical process1
    • Victory, P.; Borrell, J. I.; Vidal-Ferran, A.; Seoane, C.; Soto, J. L. The reaction of malononitrile with chalcone: A controversial chemical process1. Tetrahedron Lett. 1991, 32, 5375-5378.
    • (1991) Tetrahedron Lett , vol.32 , pp. 5375-5378
    • Victory, P.1    Borrell, J.I.2    Vidal-Ferran, A.3    Seoane, C.4    Soto, J.L.5
  • 13
    • 0242391193 scopus 로고
    • A simple synthesis of 2-methoxypyridine-3-carbonitriles
    • Victory, P. J.; Borrell, J. I.; Vidal-Ferran, A. A simple synthesis of 2-methoxypyridine-3-carbonitriles. Heterocycles 1993, 36, 769-776.
    • (1993) Heterocycles , vol.36 , pp. 769-776
    • Victory, P.J.1    Borrell, J.I.2    Vidal-Ferran, A.3
  • 14
    • 0028895677 scopus 로고
    • A non-obvious reaction pathway in the formation of 2-aminobenzene-1,3-dicarbonitriles from α,β-unsaturated ketones or aldehydes
    • Victory, P.; Alvarez-Larena, A.; Germain, G.; Kessels, R.; Piniella, J. F.; VidaI-Ferran, A. A non-obvious reaction pathway in the formation of 2-aminobenzene-1,3-dicarbonitriles from α,β-unsaturated ketones or aldehydes. Tetrahedron 1995, 51, 235-242.
    • (1995) Tetrahedron , vol.51 , pp. 235-242
    • Victory, P.1    Alvarez-Larena, A.2    Germain, G.3    Kessels, R.4    Piniella, J.F.5    VidaI-Ferran, A.6
  • 15
    • 17044427161 scopus 로고    scopus 로고
    • Parallel synthesis of strongly fluorescent polysubstituted 2,6-dicyanoanilines via microwave-promoted multicomponent reaction
    • Cui, S. L.; Lin, X. F.; Wang, Y. G. Parallel synthesis of strongly fluorescent polysubstituted 2,6-dicyanoanilines via microwave-promoted multicomponent reaction. J. Org. Chem. 2005, 70, 2866-2869.
    • (2005) J. Org. Chem , vol.70 , pp. 2866-2869
    • Cui, S.L.1    Lin, X.F.2    Wang, Y.G.3
  • 16
    • 33846698218 scopus 로고    scopus 로고
    • An efficient and facile synthesis of 2-Amino-4,6-diarylbenzene-1,3-dicarbonitrile and 1,2-dihydro-2-oxo-4,6-diarylpyridine-3-carbonitrile under solvent-free conditions
    • Rong, L. C.; Li, X. Y.; Wang, H. Y.; Shi, D. Q.; Tu, S. J. An efficient and facile synthesis of 2-Amino-4,6-diarylbenzene-1,3-dicarbonitrile and 1,2-dihydro-2-oxo-4,6-diarylpyridine-3-carbonitrile under solvent-free conditions. Chem. Lett. 2006, 35, 1314-1315.
    • (2006) Chem. Lett , vol.35 , pp. 1314-1315
    • Rong, L.C.1    Li, X.Y.2    Wang, H.Y.3    Shi, D.Q.4    Tu, S.J.5
  • 17
    • 33747588050 scopus 로고    scopus 로고
    • Efficient synthesis of tetrahydrobenzo[b]pyrans under solvent-free conditions at room temperature
    • Rong, L. C.; Li, X. Y.; Wang, H. Y.; Shi, D. Q.; Tu, S. J.; Zhuang, Q. Y. Efficient synthesis of tetrahydrobenzo[b]pyrans under solvent-free conditions at room temperature. Synth. Commun. 2006, 36, 2363-2369.
    • (2006) Synth. Commun , vol.36 , pp. 2363-2369
    • Rong, L.C.1    Li, X.Y.2    Wang, H.Y.3    Shi, D.Q.4    Tu, S.J.5    Zhuang, Q.Y.6
  • 18
    • 33747611904 scopus 로고    scopus 로고
    • Efficient green procedure for the Knoevenagel condensation under solventfree conditions
    • Rong, L. C.; Li, X. Y.; Wang, H. Y.; Shi, D. Q.; Tu, S. J.; Zhuang, Q. Y. Efficient green procedure for the Knoevenagel condensation under solventfree conditions. Synth. Commun. 2006, 36, 2407-2412.
    • (2006) Synth. Commun , vol.36 , pp. 2407-2412
    • Rong, L.C.1    Li, X.Y.2    Wang, H.Y.3    Shi, D.Q.4    Tu, S.J.5    Zhuang, Q.Y.6
  • 19
    • 33644981692 scopus 로고    scopus 로고
    • 2-[1-(3,4-Dichlorophenyl)-3-oxo-3-phenylpropyl]-3,4-dihydro-2H-naphthalen-1-one
    • Rong, L. C.; Li, X. Y.; Yao, C. S.; Wang, H. Y.; Shi, D. Q. 2-[1-(3,4-Dichlorophenyl)-3-oxo-3-phenylpropyl]-3,4-dihydro-2H-naphthalen-1-one. Acta Crys. 2006, E62, o35-o36.
    • (2006) Acta Crys , vol.E62
    • Rong, L.C.1    Li, X.Y.2    Yao, C.S.3    Wang, H.Y.4    Shi, D.Q.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.