-
1
-
-
0037028002
-
Synthesis and antimycobacterial activity of pyrazine and quinoxaline derivatives
-
Seitz, L. E.; Suling, W. J.; Reynolds, R. C. Synthesis and antimycobacterial activity of pyrazine and quinoxaline derivatives. J. Med. Chem. 2002, 45, 5604.
-
(2002)
J. Med. Chem
, vol.45
, pp. 5604
-
-
Seitz, L.E.1
Suling, W.J.2
Reynolds, R.C.3
-
2
-
-
0035942520
-
Design, synthesis, and biological evaluation of analogues of the antitumor agent, 2-{4-[(7-chloro-2-quinoxalinyl) oxy]phenoxy}propionic acid (XK469)
-
(a) Hazeldine, S. T.; Polin, L.; Kushner, J.; Paluch, J.; White, K.; Edelstein, M.; Palomino, E.; Corbett, T. H.; Horwitz, J. P. Design, synthesis, and biological evaluation of analogues of the antitumor agent, 2-{4-[(7-chloro-2-quinoxalinyl) oxy]phenoxy}propionic acid (XK469). J. Med. Chem. 2001, 44, 1758;
-
(2001)
J. Med. Chem
, vol.44
, pp. 1758
-
-
Hazeldine, S.T.1
Polin, L.2
Kushner, J.3
Paluch, J.4
White, K.5
Edelstein, M.6
Palomino, E.7
Corbett, T.H.8
Horwitz, J.P.9
-
3
-
-
0037019262
-
Synthesis and biological evaluation of some bioisosteres and congeners of the antitumor agent, 2-{4-[(7-Chloro-2-quinoxalinyl)oxy]phenoxy}propionic acid (XK469)
-
(b) Hazeldine, S. T.; Polin, L.; Kushner, J.; White, K.; Bouregeois, N. M.; Crantz, B.; Palomino, E.; Corbett, T. H.; Horwitz, J. P. Synthesis and biological evaluation of some bioisosteres and congeners of the antitumor agent, 2-{4-[(7-Chloro-2-quinoxalinyl)oxy]phenoxy}propionic acid (XK469). J. Med. Chem. 2002, 45, 3130.
-
(2002)
J. Med. Chem
, vol.45
, pp. 3130
-
-
Hazeldine, S.T.1
Polin, L.2
Kushner, J.3
White, K.4
Bouregeois, N.M.5
Crantz, B.6
Palomino, E.7
Corbett, T.H.8
Horwitz, J.P.9
-
4
-
-
0016833102
-
Structure revision of the antibiotic echinomycin
-
Dell, A.; William, D. H.; Morris, H. R.; Smith, G. A.; Feeney, J.; Roberts, G. C. K. Structure revision of the antibiotic echinomycin. J. Am. Chem. Soc. 1975, 97, 2497.
-
(1975)
J. Am. Chem. Soc
, vol.97
, pp. 2497
-
-
Dell, A.1
William, D.H.2
Morris, H.R.3
Smith, G.A.4
Feeney, J.5
Roberts, G.C.K.6
-
5
-
-
0029899585
-
Tyrphostins 5: Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: Structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins
-
Gazit, A.; App, H.; McMahon, G.; Chen, J.; Levitzki, A.; Bohmer, F. D. Tyrphostins 5: Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: Structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins. J. Med. Chem. 1996, 39, 2170.
-
(1996)
J. Med. Chem
, vol.39
, pp. 2170
-
-
Gazit, A.1
App, H.2
McMahon, G.3
Chen, J.4
Levitzki, A.5
Bohmer, F.D.6
-
6
-
-
0032562748
-
Interactions of the antiviral quinoxaline derivative 9-OH-B220 {2,3-dimethyl-6-(dimethylaminoethyl)-9-hydroxy-6H-indolo-[2,3-b]quinoxaline} with duplex and triplex forms of synthetic DNA and RNA
-
Sehlstedt, U.; Aich, P.; Bergman, J.; Vallberg, H.; Norden, B.; Graslund, A. Interactions of the antiviral quinoxaline derivative 9-OH-B220 {2,3-dimethyl-6-(dimethylaminoethyl)-9-hydroxy-6H-indolo-[2,3-b]quinoxaline} with duplex and triplex forms of synthetic DNA and RNA. J. Mol. Biol. 1998, 278, 31.
-
(1998)
J. Mol. Biol
, vol.278
, pp. 31
-
-
Sehlstedt, U.1
Aich, P.2
Bergman, J.3
Vallberg, H.4
Norden, B.5
Graslund, A.6
-
7
-
-
0034842923
-
Synthesis and device characterisation of side-chain polymer electron transport materials for organic semiconductor applications
-
Dailey, S.; Feast, J. W.; Peace, R. J.; Till, S.; Sage, I. C.; Wood, E. L. Synthesis and device characterisation of side-chain polymer electron transport materials for organic semiconductor applications. J. Mat. Chem. 2001, 11, 2238.
-
(2001)
J. Mat. Chem
, vol.11
, pp. 2238
-
-
Dailey, S.1
Feast, J.W.2
Peace, R.J.3
Till, S.4
Sage, I.C.5
Wood, E.L.6
-
8
-
-
0030213929
-
Use of poly(phenyl quinoxaline) as an electron transport material in polymer light-emitting diodes
-
O'Brien, D.; Weaver, M. S.; Lidzey, D. G.; Bradley, D. D. C. Use of poly(phenyl quinoxaline) as an electron transport material in polymer light-emitting diodes. Appl. Phys. Lett. 1996, 69, 881.
-
(1996)
Appl. Phys. Lett
, vol.69
, pp. 881
-
-
O'Brien, D.1
Weaver, M.S.2
Lidzey, D.G.3
Bradley, D.D.C.4
-
9
-
-
18144408330
-
Chromophore-labeled quinoxaline derivatives as efficient electroluminescent materials
-
Justin Thomas, K. R.; Marappan, V.; Jiann, T. L.; Chang-Hao, C.; Yu-ai, T. Chromophore-labeled quinoxaline derivatives as efficient electroluminescent materials. Chem. Mater. 2005, 17, 1860.
-
(2005)
Chem. Mater
, vol.17
, pp. 1860
-
-
Justin Thomas, K.R.1
Marappan, V.2
Jiann, T.L.3
Chang-Hao, C.4
Yu-ai, T.5
-
10
-
-
0037149976
-
Quinoxaline-oligopyrroles: Improved pyrrole-based anion receptors
-
Jonathan, L. S.; Hiromitsu, M.; Toshihisa, M.; Vincent, M. L.; Hiroyuki, F. Quinoxaline-oligopyrroles: Improved pyrrole-based anion receptors. Chem. Commun. 2002, 862.
-
(2002)
Chem. Commun
, pp. 862
-
-
Jonathan, L.S.1
Hiromitsu, M.2
Toshihisa, M.3
Vincent, M.L.4
Hiroyuki, F.5
-
11
-
-
0037073214
-
Quinoxaline-bridged porphyrinoids
-
(a) Jonathan, L. S.; Hiromitsu, M.; Toshihisa, M.; Vincent, M. L.; Hiroyuki, F. Quinoxaline-bridged porphyrinoids. J. Am. Chem. Soc. 2002, 124, 13474;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 13474
-
-
Jonathan, L.S.1
Hiromitsu, M.2
Toshihisa, M.3
Vincent, M.L.4
Hiroyuki, F.5
-
12
-
-
1342306675
-
Quinoxaline excision: A novel approach to tri- and diquinoxaline cavitands
-
(b) Peter, P. C.; Gang, Z.; Grace, A. M.; Carlos, H.; Linda, M. G. T. Quinoxaline excision: A novel approach to tri- and diquinoxaline cavitands. Org. Lett. 2004, 6, 333.
-
(2004)
Org. Lett
, vol.6
, pp. 333
-
-
Peter, P.C.1
Gang, Z.2
Grace, A.M.3
Carlos, H.4
Linda, M.G.T.5
-
13
-
-
3943058154
-
-
Sascha, O.; Rudiger, F. Quinoxalinodehydroannulenes: A novel class of carbon-rich materials. Synlett 2004, 1509.
-
Sascha, O.; Rudiger, F. Quinoxalinodehydroannulenes: A novel class of carbon-rich materials. Synlett 2004, 1509.
-
-
-
-
14
-
-
0037034055
-
Molecular design and evaluation of quinoxaline-carbohydrate hybrids as novel and efficient photo-induced GG-selective DNA cleaving agents
-
(a) Kazunobu, T.; Ryusuke, T.; Tomohiro, O.; Shuichi, M. Molecular design and evaluation of quinoxaline-carbohydrate hybrids as novel and efficient photo-induced GG-selective DNA cleaving agents. Chem. Commun. 2002, 212;
-
(2002)
Chem. Commun
, pp. 212
-
-
Kazunobu, T.1
Ryusuke, T.2
Tomohiro, O.3
Shuichi, M.4
-
15
-
-
0038441601
-
Synthesis of 5,12-dioxocyclam nickel(II) complexes having quinoxaline substituents at the 6 and 13 positions as potential DNA bis-intercalating and cleaving agents
-
(b) Hegedus, L. S.; Marc, M. G.; Jory, J. W.; Joseph, P. B. Synthesis of 5,12-dioxocyclam nickel(II) complexes having quinoxaline substituents at the 6 and 13 positions as potential DNA bis-intercalating and cleaving agents. J. Org. Chem. 2003, 68, 4179.
-
(2003)
J. Org. Chem
, vol.68
, pp. 4179
-
-
Hegedus, L.S.1
Marc, M.G.2
Jory, J.W.3
Joseph, P.B.4
-
16
-
-
51849094345
-
Supplement II
-
E. C. Taylor, P. Wipf Eds, John Wiley & Sons: NJ
-
Brown, D. J. Quinoxalines: Supplement II. In The Chemistry of Heterocyclic Compounds; E. C. Taylor, P. Wipf (Eds.); John Wiley & Sons: NJ, 2004.
-
(2004)
The Chemistry of Heterocyclic Compounds
-
-
Brown, D.J.Q.1
-
17
-
-
0037182322
-
Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines
-
Antoniotti, S.; Donach, E. Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines. Tetrahedron Lett. 2002, 43, 3971.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 3971
-
-
Antoniotti, S.1
Donach, E.2
-
18
-
-
0035813415
-
Solid-phase synthesis of quinoxalines on SynPhase lanterns
-
Wu, Z.; Ede, N. J. Solid-phase synthesis of quinoxalines on SynPhase lanterns. Tetrahedron Lett. 2001, 42, 8115.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 8115
-
-
Wu, Z.1
Ede, N.J.2
-
19
-
-
0034707362
-
Synthesis of quinoxalines by cyclization of α-arylimino oximes of α-dicarbonyl compounds
-
Xekoukoulotakis, N. P.; Hadjiantonious, M. C. P.; Maroulis, A. J. Synthesis of quinoxalines by cyclization of α-arylimino oximes of α-dicarbonyl compounds. Tetrahedron Lett. 2000, 41, 10299.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 10299
-
-
Xekoukoulotakis, N.P.1
Hadjiantonious, M.C.P.2
Maroulis, A.J.3
-
20
-
-
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
-
21
-
-
24944446763
-
An efficient protocol for the synthesis of quinoxaline derivatives at room temperature 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 temperature 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
-
22
-
-
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
-
23
-
-
33645404779
-
Cerium(IV) ammonium nitrate (CAN) as a catalyst in tap water: A simple, proficient, and green approach for the synthesis of quinoxalines
-
More, S. V.; Sastry, M. N. V.; Yao, C.-F. Cerium(IV) ammonium nitrate (CAN) as a catalyst in tap water: A simple, proficient, and green approach for the synthesis of quinoxalines. Green Chem. 2006, 8, 91.
-
(2006)
Green Chem
, vol.8
, pp. 91
-
-
More, S.V.1
Sastry, M.N.V.2
Yao, C.-F.3
-
24
-
-
33845996219
-
-
2O. Catal. Commun. 2007, 8, 211;
-
2O. Catal. Commun. 2007, 8, 211;
-
-
-
-
25
-
-
34447503639
-
Zn[(L)proline]: A powerful catalyst for the very fast synthesis of quinoxaline derivatives at room temperature
-
(b) Heravi, M. M.; Tehrani, M. H.; Bakhtiari, K.; Oskooie, H. A. Zn[(L)proline]: A powerful catalyst for the very fast synthesis of quinoxaline derivatives at room temperature. Catal. Commun. 2007, 8, 1341.
-
(2007)
Catal. Commun
, vol.8
, pp. 1341
-
-
Heravi, M.M.1
Tehrani, M.H.2
Bakhtiari, K.3
Oskooie, H.A.4
-
26
-
-
0347417134
-
Solvents for synthesis and catalysis
-
(a) Welton, T. Solvents for synthesis and catalysis. Chem. Rev. 1999, 99, 2071;
-
(1999)
Chem. Rev
, vol.99
, pp. 2071
-
-
Welton, T.1
-
27
-
-
0000034575
-
Ionic liquids - New solutions for transition metal catalysis
-
(b) Wasserscheid, P.; Keim, W. Ionic liquids - New solutions for transition metal catalysis. Angew. Chem., Int. Ed. Eng. 2000, 39, 3772;
-
(2000)
Angew. Chem., Int. Ed. Eng
, vol.39
, pp. 3772
-
-
Wasserscheid, P.1
Keim, W.2
-
28
-
-
0035824303
-
Catalytic reactions in ionic liquids
-
(c) Sheldon, R. Catalytic reactions in ionic liquids. Chem. Commun. 2001, 2399;
-
(2001)
Chem. Commun
, pp. 2399
-
-
Sheldon, R.1
-
29
-
-
57249093659
-
A short history of ionic liquids-From molten salts to neoteric solvents
-
(d) Wilkes, J. S. A short history of ionic liquids-From molten salts to neoteric solvents. Green Chem. 2002, 4, 73;
-
(2002)
Green Chem
, vol.4
, pp. 73
-
-
Wilkes, J.S.1
-
30
-
-
12344296667
-
Chemical and biochemical transformations in ionic liquids
-
(e) Jain, N.; Kumar, A.; Chauhan, S.; Chauhan, S. M. S. Chemical and biochemical transformations in ionic liquids. Tetrahedron 2005, 61, 1015.
-
(2005)
Tetrahedron
, vol.61
, pp. 1015
-
-
Jain, N.1
Kumar, A.2
Chauhan, S.3
Chauhan, S.M.S.4
-
31
-
-
0344391969
-
Ionic liquid-promoted regiospecific friedlander annulation: Novel synthesis of quinolines and fused polycyclic quinolines
-
(a) Palimkar, S. S.; Siddiqui, S. A.; Daniel, T.; Lahoti, R. J.; Srinivasan, K. V. Ionic liquid-promoted regiospecific friedlander annulation: Novel synthesis of quinolines and fused polycyclic quinolines. J. Org. Chem. 2003, 68, 9371;
-
(2003)
J. Org. Chem
, vol.68
, pp. 9371
-
-
Palimkar, S.S.1
Siddiqui, S.A.2
Daniel, T.3
Lahoti, R.J.4
Srinivasan, K.V.5
-
32
-
-
33846984926
-
Efficient synthesis of 3,5,6-trisubstituted-1,2,4-triazines in the Brønsted acidic ionic liquid, 1-n-butylimidazolium tetrafluoroborate ([Hbim]BF4)
-
(b) Potewar, T. M.; Daniel, T.; Lahoti, R. J.; Srinivasan, K. V. Efficient synthesis of 3,5,6-trisubstituted-1,2,4-triazines in the Brønsted acidic ionic liquid, 1-n-butylimidazolium tetrafluoroborate ([Hbim]BF4). Synth. Commun. 2007, 37, 261;
-
(2007)
Synth. Commun
, vol.37
, pp. 261
-
-
Potewar, T.M.1
Daniel, T.2
Lahoti, R.J.3
Srinivasan, K.V.4
-
33
-
-
33846781421
-
-
Potewar, T. M.; Siddiqui, S. A.; Lahoti, R. J.; Srinivasan, K. V. Efficient and rapid synthesis of 1-substituted-1H-1,2,3,4-tetrazoles in the acidic ionic liquid 1-n-butylimidazolium tetrafluoroborate. Tetrahedron Lett. 2007, 48, 1721;
-
(c) Potewar, T. M.; Siddiqui, S. A.; Lahoti, R. J.; Srinivasan, K. V. Efficient and rapid synthesis of 1-substituted-1H-1,2,3,4-tetrazoles in the acidic ionic liquid 1-n-butylimidazolium tetrafluoroborate. Tetrahedron Lett. 2007, 48, 1721;
-
-
-
-
34
-
-
34648823732
-
Efficient synthesis of 2,4-disubstituted thiazoles using ionic liquid under ambient conditions: A practical approach towards the synthesis of fanetizole
-
(d) Potewar, T. M.; Ingale, S. A.; Srinivasan, K. V. Efficient synthesis of 2,4-disubstituted thiazoles using ionic liquid under ambient conditions: A practical approach towards the synthesis of fanetizole. Tetrahedron 2007, 63, 11066.
-
(2007)
Tetrahedron
, vol.63
, pp. 11066
-
-
Potewar, T.M.1
Ingale, S.A.2
Srinivasan, K.V.3
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