-
1
-
-
15444370985
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
29
-
-
30344481105
-
Synthesis and antiprotozoal activity of some new synthetic substituted quinoxalines
-
Hui, X.; Desrivot, J.; Bories, C.; Loiseau, P. M.; Franck, X.; Hocquemiller, R.; Figade're, B. Synthesis and antiprotozoal activity of some new synthetic substituted quinoxalines. Bioorg. Med. Chem. Lett., 2006, 16, 815.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 815
-
-
Hui, X.1
Desrivot, J.2
Bories, C.3
Loiseau, P.M.4
Franck, X.5
Hocquemiller, R.6
Figade're, B.7
-
30
-
-
33847037381
-
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
-
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
|