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Volumn 7, Issue 3, 2010, Pages 208-211

Niobium (V) chloride: An efficient catalyst for the synthesis of quinoxalines

Author keywords

Diketones; Niobium chloride; Ortho phenylenediamines; Quinoxalines

Indexed keywords


EID: 77951470153     PISSN: 15701786     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017810791112432     Document Type: Article
Times cited : (10)

References (31)
  • 1
    • 15444370985 scopus 로고    scopus 로고
    • Synthesis of new quinoxalines-2-carbo xylate 1,4-dioxide derivatives as anti- mycobacterium tuberculosis agents
    • Jaso, A.; Zarranz, B.; Aldana, I.; Monge, A. Synthesis of new quinoxalines-2-carbo xylate 1,4-dioxide derivatives as anti- mycobacterium tuberculosis agents. J. Med. Chem., 2005, 48, 2019.
    • (2005) J. Med. Chem. , vol.48 , pp. 2019
    • Jaso, A.1    Zarranz, B.2    Aldana, I.3    Monge, A.4
  • 2
    • 2342632050 scopus 로고    scopus 로고
    • The significant effect of the carbohydrate structures on the DNA photocleavage of the quinoxaline-carbohydrate hybrids
    • Toshima, T.; Ozawa, T.; Kimura, T.; Matsumara, S. The significant effect of the carbohydrate structures on the DNA photocleavage of the quinoxaline-carbohydrate hybrids. Bioorg. Med. Chem. Lett., 2004, 74, 2777.
    • (2004) Bioorg. Med. Chem. Lett. , vol.74 , pp. 2777
    • Toshima, T.1    Ozawa, T.2    Kimura, T.3    Matsumara, S.4
  • 3
    • 0025306964 scopus 로고
    • 4-Amino [1,2,4] triazolo [4,3-a] quinoxalines. A novel class of potent adenosine receptor anta gonists and potential rapid- onset antidepressants
    • Sarges, R.; Howard, H. R.; Browne, R. G.; Lebel, L. A.; Seymour, P. A. 4-Amino [1,2,4] triazolo [4,3-a] quinoxalines. A novel class of potent adenosine receptor anta gonists and potential rapid- onset antidepressants. J. Med. Chem., 1990, 33, 2240.
    • (1990) J. Med. Chem. , vol.33 , pp. 2240
    • Sarges, R.1    Howard, H.R.2    Browne, R.G.3    Lebel, L.A.4    Seymour, P.A.5
  • 4
    • 0034842923 scopus 로고    scopus 로고
    • Synthesis and device characterization of side-chain polymer electron transport materials for organic semiconductor applications
    • Dailey, S.; Feast, J. W.; Peace, R. J.; Sage, I. C.; Till, S.; Wood, E.L. Synthesis and device characterization of side-chain polymer electron transport materials for organic semiconductor applications. J. Mater. Chem., 2001, 11, 2238.
    • (2001) J. Mater. Chem. , vol.11 , pp. 2238
    • Dailey, S.1    Feast, J.W.2    Peace, R.J.3    Sage, I.C.4    Till, S.5    Wood, E.L.6
  • 5
    • 23744463590 scopus 로고    scopus 로고
    • Molecular iodine: A powerful catalyst for the easy and efficient synthesis of quinoxalines
    • More, S. V.; Sastry, M. N. V.; Wang, C. C.; Yao, C. F. Molecular iodine: a powerful catalyst for the easy and efficient synthesis of quinoxalines. Tetrahedron Lett., 2005, 46, 6345.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 6345
    • More, S.V.1    Sastry, M.N.V.2    Wang, C.C.3    Yao, C.F.4
  • 6
    • 55649115122 scopus 로고    scopus 로고
    • Synthesis of 6H-indolo[2,3-b]quinoxaline-N-glycosides and their cytotoxic activity against human ceratinocytes (HaCaT)
    • Driller, K. M.; Libnow, S.; Hein, M.; Harms, M.; Wende, K.; Lalk, M.; Michalik, D.; Reinke, H.; Langer, P. Synthesis of 6H-indolo[2,3-b]quinoxaline-N- glycosides and their cytotoxic activity against human ceratinocytes (HaCaT). Org. Biomol. Chem., 2008, 6, 4218.
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 4218
    • Driller, K.M.1    Libnow, S.2    Hein, M.3    Harms, M.4    Wende, K.5    Lalk, M.6    Michalik, D.7    Reinke, H.8    Langer, P.9
  • 7
    • 33750091068 scopus 로고    scopus 로고
    • Diverse 2- carboxamide-3-amino-sub stituted quinoxalines. Synthesis and reactivity investigation for library generation
    • Kowalski, J. A.; Leonard, S. F.; Jr, Lee, G. E. Diverse 2- carboxamide-3-amino-sub stituted quinoxalines. Synthesis and reactivity investigation for library generation. J. Comb. Chem., 2006, 8, 774.
    • (2006) J. Comb. Chem. , vol.8 , pp. 774
    • Kowalski, J.A.1    Leonard Jr., S.F.2    Lee, G.E.3
  • 8
    • 61549141761 scopus 로고    scopus 로고
    • y (M = Al, Ga, In and La) mixed metal oxides supported on MCM-41 meso porous molecular sieves
    • y (M = Al, Ga, In and La) mixed metal oxides supported on MCM-41 meso porous molecular sieves. Appl. Catal. A., 2009, 357, 184.
    • (2009) Appl. Catal. A. , vol.357 , pp. 184
    • Ajaikumar, S.1    Pandurangan, A.2
  • 9
    • 34247533292 scopus 로고    scopus 로고
    • Benign approaches for the micro wave-assisted synthesis of quinoxalines
    • Mohsenzadeh, F.; Aghapoor, K.; Darabi, H. R. Benign approaches for the micro wave-assisted synthesis of quinoxalines. J. Braz. Chem. Soc., 2007, 78, 297.
    • (2007) J. Braz. Chem. Soc. , vol.78 , pp. 297
    • Mohsenzadeh, F.1    Aghapoor, K.2    Darabi, H.R.3
  • 10
    • 0037182322 scopus 로고    scopus 로고
    • Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines
    • Antoniotti, S.; Dunach, E. Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines. Tetrahedron Lett. 2002, 43(22), 3971-3973.
    • (2002) Tetrahedron Lett. , vol.43 , Issue.22 , pp. 3971-3973
    • Antoniotti, S.1    Dunach, E.2
  • 12
    • 34250864992 scopus 로고    scopus 로고
    • Dipolar cycloaddition of ethyl isocyanoacetate to 3-chloro-2- (methylthio)/2-(methylsulfonyl) quinoxalines: Highly regio and chemoselective synthesis of substituted imidazo[1,5-a] quinoxaline-3-carboxylates
    • Sundaram, G. S. M.; Singh, B.; Venkatesh, C.; Ila, H.; Junjappa, H. Dipolar cycloaddition of ethyl isocyanoacetate to 3-chloro-2- (methylthio)/2-(methylsulfonyl) quinoxalines: highly regio and chemoselective synthesis of substituted imidazo[1,5-a] quinoxaline-3-carboxylates. J. Org. Chem., 2007, 72, 5020.
    • (2007) J. Org. Chem. , vol.72 , pp. 5020
    • Sundaram, G.S.M.1    Singh, B.2    Venkatesh, C.3    Ila, H.4    Junjappa, H.5
  • 13
    • 52949097250 scopus 로고    scopus 로고
    • Manganese octahedral molecular sieves catalyzed tandem process for synthesis of quinoxalines
    • Sithambaram, S.; Ding, Y.; Li, W.; Shen, X.; Gaenzler, F.; Suib, S. L. Manganese octahedral molecular sieves catalyzed tandem process for synthesis of quinoxalines. Green Chem., 2008, 10, 1029.
    • (2008) Green Chem. , vol.10 , pp. 1029
    • Sithambaram, S.1    Ding, Y.2    Li, W.3    Shen, X.4    Gaenzler, F.5    Suib, S.L.6
  • 14
    • 34447501915 scopus 로고    scopus 로고
    • Uncatalyzed condensation between aryl-1,2-diamines and diethyl bromomalonate: A one-pot access to substituted ethyl 3-hydroxy quinoxaline-2-carboxylates
    • Haldar, P.; Dutta, B.; Guin, J.; Ray, J. K. Uncatalyzed condensation between aryl-1,2-diamines and diethyl bromomalonate: a one-pot access to substituted ethyl 3-hydroxy quinoxaline-2-carboxylates. Tetrahedron Lett., 2007, 48, 5855.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 5855
    • Haldar, P.1    Dutta, B.2    Guin, J.3    Ray, J.K.4
  • 15
    • 33846236966 scopus 로고    scopus 로고
    • An efficient synthesis of quinoxaline deri vatives from 4-chloro-a-d-galactose and their cytotoxic activities
    • Yan, L.; Liu, F. W.; Dai, G. F.; Liu, H. M. An efficient synthesis of quinoxaline deri vatives from 4-chloro-a-d-galactose and their cytotoxic activities. Bioorg. Med. Chem. Lett., 2007, 17, 609.
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 609
    • Yan, L.1    Liu, F.W.2    Dai, G.F.3    Liu, H.M.4
  • 16
    • 34548536999 scopus 로고    scopus 로고
    • Copper-catalyzed oxidative cyclization of a- hydroxyketones with o-phenylenediamines leading to quinoxalines
    • Cho, C. S.; Ohb, S. G. Copper-catalyzed oxidative cyclization of a- hydroxyketones with o-phenylenediamines leading to quinoxalines. J. Mol. Catal A., 2007, 276, 205.
    • (2007) J. Mol. Catal A. , vol.276 , pp. 205
    • Cho, C.S.1    Ohb, S.G.2
  • 17
    • 42049100636 scopus 로고    scopus 로고
    • 2-catalyzed synthesis of quinoxalines from a- diazoketones and aryl 1,2-di amines
    • 2-catalyzed synthesis of quinoxalines from a- diazoketones and aryl 1,2-di amines. Chem. Lett., 2008, 37, 348.
    • (2008) Chem. Lett. , vol.37 , pp. 348
    • Yadav, J.S.1    Reddy, B.V.S.2    Rao, Y.G.3    Narsaiah, A.V.4
  • 18
    • 33847009461 scopus 로고    scopus 로고
    • Three-component tandem reactions of (2-arylsulfanyl-3-aryl-2-oxiranyl) (aryl)methanones and o-phenylenediamine: Formation of quinoxalines
    • Nasar, M. K.; Kumar, R. R.; Perumal, S. Three-component tandem reactions of (2-arylsulfanyl-3-aryl-2-oxiranyl)(aryl)methanones and o-phenylenediamine: formation of quinoxalines. Tetrahedron Lett., 2007, 48, 2155.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 2155
    • Nasar, M.K.1    Kumar, R.R.2    Perumal, S.3
  • 19
    • 22144448620 scopus 로고    scopus 로고
    • Direct solid-phase synthesis of quinoxaline-containing peptides
    • Staszewska, A.; Stefanowicz, P.; Szewezuk, Z. Direct solid-phase synthesis of quinoxaline-containing peptides. Tetrahedron Lett., 2005, 46, 5525.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 5525
    • Staszewska, A.1    Stefanowicz, P.2    Szewezuk, Z.3
  • 20
    • 24944446763 scopus 로고    scopus 로고
    • An efficient protocol for the synthesis of quinoxaline derivatives at room tempe rature using molecular iodine as the catalyst
    • Bhosale, R. S.; Sarda, S. R.; Ardhapure, S. S.; Jadhav, W. N.; Bhusare, S. R.; Pawar, R. P. An efficient protocol for the synthesis of quinoxaline derivatives at room tempe rature using molecular iodine as the catalyst. Tetrahedron Lett., 2005, 46, 7183.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 7183
    • Bhosale, R.S.1    Sarda, S.R.2    Ardhapure, S.S.3    Jadhav, W.N.4    Bhusare, S.R.5    Pawar, R.P.6
  • 21
    • 34249893387 scopus 로고    scopus 로고
    • Ketones as a new synthon for quinoxaline synthesis
    • Cho, C. S.; Ren, W. X.; Shim, S. C. Ketones as a new synthon for quinoxaline synthesis. Tetrahedron Lett., 2007, 48, 4665.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 4665
    • Cho, C.S.1    Ren, W.X.2    Shim, S.C.3
  • 22
    • 62349141160 scopus 로고    scopus 로고
    • Heterocyclizations via TosMIC -based multicomponent reactions: A new approach to one-pot facile synthesis of substituted quinoxalines derivatives
    • Neochoritis, C.; Stephanatou, J. S.; Tsoleridis, C. A. Heterocyclizations via TosMIC -based multicomponent reactions: a new approach to one-pot facile synthesis of substituted quinoxalines derivatives. Synlett., 2009, 2, 302.
    • (2009) Synlett. , vol.2 , pp. 302
    • Neochoritis, C.1    Stephanatou, J.S.2    Tsoleridis, C.A.3
  • 23
    • 55549140786 scopus 로고    scopus 로고
    • Gallium (III) triflate- catalyzed synthesis of quinoxaline derivatives
    • Cai, J. J.; Zou, J. P.; Pan, X. Q.; Zhang, W. Gallium (III) triflate- catalyzed synthesis of quinoxaline derivatives. Tetrahedron Lett., 2008, 49, 7386.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 7386
    • Cai, J.J.1    Zou, J.P.2    Pan, X.Q.3    Zhang, W.4
  • 24
    • 33847687134 scopus 로고    scopus 로고
    • Efficient, convenient and reusable polyaniline-sulfate salt catalyst for the synthesis of quinoxaline derivatives
    • Srinivas, C.; Kumar, C. N. S. S. P.; Rao, V. J.; Palaniappan, S. Efficient, convenient and reusable polyaniline-sulfate salt catalyst for the synthesis of quinoxaline derivatives. J. Mol. Catal. A., 2007, 265, 227.
    • (2007) J. Mol. Catal. A. , vol.265 , pp. 227
    • Srinivas, C.1    Kumar, C.N.S.S.P.2    Rao, V.J.3    Palaniappan, S.4
  • 25
    • 2942519827 scopus 로고    scopus 로고
    • General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines
    • Zhao, Z.; Wisnoski, D. D.; Wolkenberg, S. E.; Leister, W. H.; Wang, Y.; Lindsley, C. W. General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines. Tetrahedron Lett., 2004, 45, 4873.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 4873
    • Zhao, Z.1    Wisnoski, D.D.2    Wolkenberg, S.E.3    Leister, W.H.4    Wang, Y.5    Lindsley, C.W.6
  • 26
    • 58149093267 scopus 로고    scopus 로고
    • A novel three- component reaction for the synthesis of N-cyclohexyl-3-aryl- quinoxaline-2-amines
    • Heravi, M. M.; Baghernejad, B.; Oskooie, H. A. A novel three- component reaction for the synthesis of N-cyclohexyl-3-aryl- quinoxaline-2-amines. Tetrahedron Lett., 2009, 50, 767.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 767
    • Heravi, M.M.1    Baghernejad, B.2    Oskooie, H.A.3
  • 27
    • 0037167079 scopus 로고    scopus 로고
    • Synthesis of 6,7-ethylenedioxy quinoxalines and pyrido [2,3-b]pyrazines as intermediates in the preparation of antineoplastic agents
    • Mateu, M.; Capilla, A. S.; Harrak, Y.; Pujol, M. D. Synthesis of 6,7-ethylenedioxy quinoxalines and pyrido [2,3-b]pyrazines as intermediates in the preparation of antineoplastic agents. Tetrahedron., 2002, 58, 5241.
    • (2002) Tetrahedron. , vol.58 , pp. 5241
    • Mateu, M.1    Capilla, A.S.2    Harrak, Y.3    Pujol, M.D.4
  • 28
    • 57549094425 scopus 로고    scopus 로고
    • Bismuth (III)-catalyzed rapid synthesis of 2,3-disubstituted quinoxalines in water
    • Yadav, J. S.; Reddy, B. V. S.; Premalatha, K.; Shankar, K. S. Bismuth (III)-catalyzed rapid synthesis of 2,3-disubstituted quinoxalines in water. Synthesis., 2008, 23, 3787.
    • (2008) Synthesis. , vol.23 , pp. 3787
    • Yadav, J.S.1    Reddy, B.V.S.2    Premalatha, K.3    Shankar, K.S.4
  • 30
    • 33847037381 scopus 로고    scopus 로고
    • Structure-activity relationship (SAR) studies of quinoxalines as novel HCV NS5B RNA-dependent RNA polymerase inhibitors
    • Rong, F.; Chow, S.; Yan, S.; Larson, G.; Hong, Z.; Wu, J. Structure-activity relationship (SAR) studies of quinoxalines as novel HCV NS5B RNA-dependent RNA polymerase inhibitors. Bioorg. Med. Chem. Lett., 2007, 17, 1663.
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 1663
    • Rong, F.1    Chow, S.2    Yan, S.3    Larson, G.4    Hong, Z.5    Wu, J.6
  • 31
    • 17144375635 scopus 로고    scopus 로고
    • Quinoxaline synthesis from a- hydroxy ketones via a tandem oxidation process using catalyzed aerobic oxidation
    • Robinson, R. S.; Taylor, R. J. K. Quinoxaline synthesis from a- hydroxy ketones via a tandem oxidation process using catalyzed aerobic oxidation. Synlett., 2005, 6, 1003.
    • (2005) Synlett. , vol.6 , pp. 1003
    • Robinson, R.S.1    Taylor, R.J.K.2


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