-
1
-
-
15444370985
-
Synthesis of new quinoxaline-2-carboxylate 1,4-dioxide derivatives as anti-Mycobacterium tuberculosis agents
-
DOI 10.1021/jm049952w
-
Jaso, A.; Zarranz, B.; Aldana, I.; Monge, A. synthesis of new quinoxaline-2-carboxylate 1,4-dioxide derivatives as anti- mycobacterium tuberculosis agents. J. Med. Chem., 2005, 48, 2019-2025. (Pubitemid 40396329)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.6
, pp. 2019-2025
-
-
Jaso, A.1
Zarranz, B.2
Aldana, I.3
Monge, A.4
-
3
-
-
2942532638
-
Quinoxaline N,N'-dioxide derivatives and related compounds as growth inhibitors of Trypanosoma cruzi. Structure-activity relationships
-
DOI 10.1016/j.bmcl.2004.04.088, PII S0960894X04006055
-
Aguirre, G.; Cerecetto, H.; Di Maio, R.; Gonzales, M.; Alfaro, M. E. M. A.; Jaso, A.; Zarranz, B.; Ortega, M. A.; Aldana, I.; Monge-Vega, A. Quinoxaline N,N'-dioxide derivatives and related compounds as growth inhibitors of Trypanosoma cruzi. Structure-activity relationships. Bioorg. Med. Chem. Lett., 2004, 14, 3835-3839. (Pubitemid 38760089)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.14
, pp. 3835-3839
-
-
Aguirre, G.1
Cerecetto, H.2
Di Maio, R.3
Gonzalez, M.4
Alfaro, M.E.M.5
Jaso, A.6
Zarranz, B.7
Ortega, M.A.8
Aldana, I.9
Monge-Vega, A.10
-
4
-
-
2342632050
-
The significant effect of the carbohydrate structures on the DNA photocleavage of the quinoxaline-carbohydrate hybrids
-
DOI 10.1016/j.bmcl.2004.03.065, PII S0960894X04004378
-
Toshima, K.; Ozawa, T.; Kimura, T.; Matsumara, S. The significant effect of the carbohydrate structures on the DNA photo cleavage of the quinoxaline-carbohydrate hybrids. Bioorg. Med. Chem. Lett., 2004, 14, 2777-2779. (Pubitemid 38569735)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.11
, pp. 2777-2779
-
-
Toshima, K.1
Ozawa, T.2
Kimura, T.3
Matsumura, S.4
-
5
-
-
0037188105
-
Oxidative cleavage of DNA by a dipyridoquinoxaline copper(II) complex in the presence of ascorbic acid
-
DOI 10.1016/S0162-0134(01)00418-4, PII S0162013401004184
-
Santra, B. K.; Reddy, P. A. N.; Neelakanta, G.; Mahadevan, S.; Nethaji, M.; Chakravarty, A. R. Oxidative cleavage of DNA by a dipyridoquinoxaline copper(II) complex in the presence of ascorbic acid. J. Inorg. Biochem., 2002, 89, 191-196. (Pubitemid 34406431)
-
(2002)
Journal of Inorganic Biochemistry
, vol.89
, Issue.3-4
, pp. 191-196
-
-
Santra, B.K.1
Reddy, P.A.N.2
Neelakanta, G.3
Mahadevan, S.4
Nethaji, M.5
Chakravarty, A.R.6
-
6
-
-
0037294869
-
Synthesis, crystal structure, and nuclease activity of planar mono-heterocyclic base copper(II) complexes
-
DOI 10.1016/S0162-0134(02)00613-X
-
Thomas, A. M.; Nethaji, M.; Mahadevan, S.; Chakravarty, A. R. Synthesis, crystal structure, and nuclease activity of planar monoheterocyclic base copper(II) complexes. J. Inorg. Biochem., 2003, 94, 171-178. (Pubitemid 36293429)
-
(2003)
Journal of Inorganic Biochemistry
, vol.94
, Issue.1-2
, pp. 171-178
-
-
Thomas, A.M.1
Nethaji, M.2
Mahadevan, S.3
Chakravarty, A.R.4
-
7
-
-
0036277334
-
Structure and coordination behavior of 2,3-bis(2- furanyl) quinoxaline
-
Wu, J.-Z.; Xu, Z.-G.; Li, Y.; Zhang, W.-G.; Zeng, H.-P.; Xu, X.; Zhou, Z.-Z. Structure and coordination behavior of 2,3-bis(2- furanyl) quinoxaline. J. Chem. Crystallogr., 2002, 32, 75-80.
-
(2002)
J. Chem. Crystallogr.
, vol.32
, pp. 75-80
-
-
Wu, J.-Z.1
Xu, Z.-G.2
Li, Y.3
Zhang, W.-G.4
Zeng, H.-P.5
Xu, X.6
Zhou, Z.-Z.7
-
8
-
-
84944048121
-
-
Katritsky, A. R.; Rees C. W.; Eds.; Pergamon: Oxford
-
Porter, A. E. A. In: Comprehensive Heterocyclic Chemistry; Katritsky, A. R.; Rees, C. W.; Eds.; Pergamon: Oxford, 1984, p. 157.
-
(1984)
Comprehensive Heterocyclic Chemistry
, pp. 157
-
-
Porter, A.E.A.1
-
9
-
-
33845537355
-
Quinoxalines: Supplement II
-
Taylor, E. C.; Wipf, P. Eds.; John Wiley & Sons: New Jersey
-
Brown, D. J. Quinoxalines: Supplement II. In: The Chemistry of Heterocyclic Compounds; Taylor, E. C.; Wipf, P. Eds.; John Wiley & Sons: New Jersey, 2004.
-
(2004)
The Chemistry of Heterocyclic Compounds
-
-
Brown, D.J.1
-
10
-
-
24944446763
-
An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using molecular iodine as the catalyst
-
DOI 10.1016/j.tetlet.2005.08.080, PII S0040403905018290
-
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, 7183-7186. (Pubitemid 41317103)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.42
, pp. 7183-7186
-
-
Bhosale, R.S.1
Sarda, S.R.2
Ardhapure, S.S.3
Jadhav, W.N.4
Bhusare, S.R.5
Pawar, R.P.6
-
11
-
-
23744463590
-
Molecular iodine: A powerful catalyst for the easy and efficient synthesis of quinoxalines
-
DOI 10.1016/j.tetlet.2005.07.026, PII S0040403905015133
-
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, 6345-6348. (Pubitemid 41140194)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.37
, pp. 6345-6348
-
-
More, S.V.1
Sastry, M.N.V.2
Wang, C.-C.3
Yao, C.-F.4
-
12
-
-
33845537940
-
A recyclable and highly effective sulfamic acid/MeOH catalytic system for the synthesis of quinoxalines at room temperature
-
DOI 10.1016/j.catcom.2006.06.033, PII S1566736706002494
-
Darabi, H. R.; Mohandessi, S.; Aghapoor, K.; Mohsenzadeh, F. A recyclable and highly effective sulfamic acid/MeOH catalytic system for the synthesis of quinoxalines at room temperature. Catal. Commun., 2007, 8, 389-392. (Pubitemid 44828641)
-
(2007)
Catalysis Communications
, vol.8
, Issue.3
, pp. 389-392
-
-
Darabi, H.R.1
Mohandessi, S.2
Aghapoor, K.3
Mohsenzadeh, F.4
-
13
-
-
39349108390
-
Montmorillonite K-10: An efficient and reusable catalyst for the synthesis of quinoxaline derivatives in water
-
DOI 10.1016/j.catcom.2007.10.024, PII S1566736707004724
-
Huang, T. K.; Wang, R.; Shi, L.; Lu, X. X. Montmorillonite K-10: An efficient and reusable catalyst for the synthesis of quinoxaline derivatives in water. Catal. Commun., 2008, 9, 1143-1147. (Pubitemid 351264824)
-
(2008)
Catalysis Communications
, vol.9
, Issue.6
, pp. 1143-1147
-
-
Huang, T.-k.1
Wang, R.2
Shi, L.3
Lu, X.-x.4
-
14
-
-
33847687134
-
Efficient, convenient and reusable polyaniline-sulfate salt catalyst for the synthesis of quinoxaline derivatives
-
DOI 10.1016/j.molcata.2006.10.018, PII S1381116906012945
-
Srinivas, C.; Kumar, C. N. S. S. P.; Jayathirtha Rao, V.; Palaniappan, S. Efficient, convenient and reusable polyanilinesulfate salt catalyst for the synthesis of quinoxaline derivatives. J. Mol. Catal. A: Chem., 2007, 265, 227-230. (Pubitemid 46357017)
-
(2007)
Journal of Molecular Catalysis A: Chemical
, vol.265
, Issue.1-2
, pp. 227-230
-
-
Srinivas, C.1
Kumar, C.N.S.S.P.2
Rao, V.J.3
Palaniappan, S.4
-
15
-
-
34248150492
-
Wells-Dawson type heteropolyacid catalyzed synthesis of quinoxaline derivatives at room temperature
-
Heravi, M. M.; Bakhtiari, Kh.; Bamoharram, F. F.; Tehrani, M. H. Wells-Dawson type heteropolyacid catalyzed synthesis of quinoxaline derivatives at room temperature. Monatsh. Chem., 2007, 138, 465-467.
-
(2007)
Monatsh. Chem.
, vol.138
, pp. 465-467
-
-
Heravi, M.M.1
Bakhtiari, Kh.2
Bamoharram, F.F.3
Tehrani, M.H.4
-
16
-
-
35148839611
-
Efficient and green method for the synthesis of 1,5-benzodiazepine and quinoxaline derivatives in water
-
DOI 10.1080/00397910701489388, PII 782881713
-
Hazarika, P.; Gogoi, P.; Konwar, D. Efficient and green method for the synthesis of 1,5-benzodiazepine and quinoxaline derivatives in water. Synth. Commun., 2007, 37, 3447-3454. (Pubitemid 47537128)
-
(2007)
Synthetic Communications
, vol.37
, Issue.19
, pp. 3447-3454
-
-
Hazarika, P.1
Gogoi, P.2
Konwar, D.3
-
17
-
-
40749091661
-
2-promoted synthesis of quinoxaline derivatives at room temperature
-
DOI 10.1002/hc.20401
-
2-promoted synthesis of quinoxaline derivatives at room temperature. Heteroatom. Chem., 2008, 19, 218-220. (Pubitemid 351378720)
-
(2008)
Heteroatom Chemistry
, vol.19
, Issue.2
, pp. 218-220
-
-
Heravi, M.M.1
Bakhtiari, K.2
Oskooie, H.A.3
Taheri, S.4
-
18
-
-
33845996219
-
2O
-
DOI 10.1016/j.catcom.2006.06.013, PII S1566736706002160
-
2O. Catal. Commun., 2007, 8, 211-214. (Pubitemid 46043570)
-
(2007)
Catalysis Communications
, vol.8
, Issue.2
, pp. 211-214
-
-
Heravi, M.M.1
Taheri, S.2
Bakhtiari, K.3
Oskooie, H.A.4
-
19
-
-
34447503639
-
Zn[(l)proline]: A powerful catalyst for the very fast synthesis of quinoxaline derivatives at room temperature
-
DOI 10.1016/j.catcom.2006.11.026, PII S1566736706004584
-
Heravi, M. M.; Tehrani, M. H.; Bakhtiari, Kh.; Oskooie, H. A. Zn[(l)proline]: A powerful catalyst for the very fast synthesis of quinoxaline derivatives at room temperature. Catal. Commun., 2007, 8, 1341-1344. (Pubitemid 47082509)
-
(2007)
Catalysis Communications
, vol.8
, Issue.9
, pp. 1341-1344
-
-
Heravi, M.M.1
Tehrani, M.H.2
Bakhtiari, K.3
Oskooie, H.A.4
-
20
-
-
33645404779
-
Cerium (IV) ammonium nitrate (CAN) as a catalyst in tap water: A simple, proficient and green approach for the synthesis of quinoxalines
-
DOI 10.1039/b510677j
-
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, 91-95. (Pubitemid 43485030)
-
(2006)
Green Chemistry
, vol.8
, Issue.1
, pp. 91-95
-
-
More, S.V.1
Sastry, M.N.V.2
Yao, C.-F.3
-
21
-
-
0037182322
-
Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines
-
DOI 10.1016/S0040-4039(02)00715-3, PII S0040403902007153
-
Antoniotti, S.; Donach, E. Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines. Tetrahedron Lett., 2002, 43, 3971-3973. (Pubitemid 34603206)
-
(2002)
Tetrahedron Letters
, vol.43
, Issue.22
, pp. 3971-3973
-
-
Antoniotti, S.1
Dunach, E.2
-
22
-
-
17144375635
-
Quinoxaline synthesis from α-hydroxy ketones via a tandem oxidation process using catalysed aerobic oxidation
-
DOI 10.1055/s-2005-864830, D01505ST
-
Robinson, R. S.; Taylor, R. J. K. Quinoxaline synthesis from α- hydroxy ketones via a tandem oxidation process using catalyzed aerobic oxidation. Synlett, 2005, 1003-1005, doi:10.1002/chin.200535186. (Pubitemid 40524274)
-
(2005)
Synlett
, Issue.6
, pp. 1003-1005
-
-
Robinson, R.S.1
Taylor, R.J.K.2
-
23
-
-
1642413403
-
Tandem oxidation processes for the preparation of nitrogen-containing heteroaromatic and heterocyclic compounds
-
Raw, S. A.; Wilfred, C. D.; Taylor, R. J. K. Tandem oxidation processes for the preparation of nitrogen-containing heteroaromatic and heterocyclic compounds. Org. Biomol. Chem., 2004, 2, 788-796.
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 788-796
-
-
Raw, S.A.1
Wilfred, C.D.2
Taylor, R.J.K.3
-
24
-
-
0141567587
-
Preparation of quinoxalines, dihydropyrazines, pyrazines and piperazines using tandem oxidation processes
-
Raw, S. A.; Wilfred, C. D.; Taylor, R. J. K. Preparation of quinoxalines, dihydropyrazines, pyrazines and piperazines using tandem oxidation processes. Chem. Commun., 2003, 2286-2287, doi:10.1002/chin.200403147. (Pubitemid 37163941)
-
(2003)
Chemical Communications
, Issue.18
, pp. 2286-2287
-
-
Raw, S.A.1
Wilfred, C.D.2
Taylor, R.J.K.3
-
25
-
-
2942519827
-
General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines
-
DOI 10.1016/j.tetlet.2004.04.144, PII S0040403904009633
-
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, 4873-4876. (Pubitemid 38738838)
-
(2004)
Tetrahedron Letters
, vol.45
, Issue.25
, pp. 4873-4876
-
-
Zhao, Z.1
Wisnoski, D.D.2
Wolkenberg, S.E.3
Leister, W.H.4
Wang, Y.5
Lindsley, C.W.6
-
26
-
-
69249162032
-
Zirconium tetrakis(dodecylsulfate) as an efficient and recyclable lewis acid- surfactant-combined catalyzed C-C and C-N bond forming under mild and environmentally benign conditions
-
Jafarpour, M.; Rezaeifard, A.; Aliabadi, M. Zirconium tetrakis(dodecylsulfate) as an efficient and recyclable lewis acid- surfactant-combined catalyzed C-C and C-N bond forming under mild and environmentally benign conditions. Lett. Org. Chem., 2009, 6, 94-99.
-
(2009)
Lett. Org. Chem.
, vol.6
, pp. 94-99
-
-
Jafarpour, M.1
Rezaeifard, A.2
Aliabadi, M.3
-
27
-
-
66349090169
-
New Catalytic Method for Ecofriendly Synthesis of Bis- and Trisindolylmethanes by Zirconyldodecylsulfate under mild conditions
-
Jafarpour, M.; Rezaeifard, A.; Golshani, T. New Catalytic Method for Ecofriendly Synthesis of Bis- and Trisindolylmethanes by Zirconyldodecylsulfate under mild conditions. J. Heterocyclic Chem., 2009, 46, 535-539.
-
(2009)
J. Heterocyclic Chem.
, vol.46
, pp. 535-539
-
-
Jafarpour, M.1
Rezaeifard, A.2
Golshani, T.3
-
28
-
-
77949518987
-
An environmentally benign catalytic method for efficient and selective nucleophilic ring opening of oxiranes by zirconium tetrakis(dodecyl sulfate)
-
Jafarpour, M.; Rezaeifard, A.; Aliabadi, M. An environmentally benign catalytic method for efficient and selective nucleophilic ring opening of oxiranes by zirconium tetrakis(dodecyl sulfate). Helv. Chem. Acta, 2010, 93, 405-413.
-
(2010)
Helv. Chem. Acta
, vol.93
, pp. 405-413
-
-
Jafarpour, M.1
Rezaeifard, A.2
Aliabadi, M.3
-
29
-
-
78751528734
-
Catalyst-Free Method for the Synthesis of Sulfonamides and Sulfonylazides
-
Jafarpour, M.; Rezaeifard, A.; Golshani, T. A Green, Catalyst-Free Method for the Synthesis of Sulfonamides and Sulfonylazides. Phosphorus Sulfur Silicon, 2011, 186, 140-148.
-
(2011)
Phosphorus Sulfur Silicon
, vol.186
, pp. 140-148
-
-
Jafarpour, M.1
Rezaeifard, A.2
Green, A.G.T.3
-
30
-
-
61849160495
-
Catalytic activity of silica gel in the synthesis of sulfonamides under mild and solventfree conditions
-
Jafarpour, M.; Rezaeifard, A.; Aliabadi, M. Catalytic activity of silica gel in the synthesis of sulfonamides under mild and solventfree conditions. Appl. Catal. A General, 2009, 358, 49-53.
-
(2009)
Appl. Catal. A General
, vol.358
, pp. 49-53
-
-
Jafarpour, M.1
Rezaeifard, A.2
Aliabadi, M.3
-
31
-
-
79951675531
-
Easy access to quinoxaline derivatives using alumina as an effective and reusable catalyst under solvent-free conditions
-
Jafarpour, M.; Rezaeifard, A.; Danehchin, M. Easy access to quinoxaline derivatives using alumina as an effective and reusable catalyst under solvent-free conditions. Appl. Catal. A General, 2011, 394, 48-51.
-
(2011)
Appl. Catal. A General
, vol.394
, pp. 48-51
-
-
Jafarpour, M.1
Rezaeifard, A.2
Danehchin, M.3
-
33
-
-
4444356919
-
4/NaI
-
DOI 10.1016/j.tetlet.2004.08.056, PII S0040403904017496
-
4/NaI. Tetrahedron Lett., 2004, 45, 7451-7454. (Pubitemid 39208385)
-
(2004)
Tetrahedron Letters
, vol.45
, Issue.40
, pp. 7451-7454
-
-
Firouzabadi, H.1
Iranpoor, N.2
Jafarpour, M.3
-
34
-
-
18844426537
-
4/NaI
-
DOI 10.1016/j.tetlet.2005.04.005, PII S0040403905007604
-
4/NaI. Tetrahedron Lett., 2005, 46, 4107-4110. (Pubitemid 40692922)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.23
, pp. 4107-4110
-
-
Firouzabadi, H.1
Iranpoor, N.2
Jafarpour, M.3
-
35
-
-
31144455721
-
2O/NaI as effective systems for reductive coupling of sulfonyl chlorides and chemoselective deoxygenation of sulfoxides
-
2O/NaI as effective systems for reductive coupling of sulfonyl chlorides and chemoselective deoxygenation of sulfoxides. J. Sulf. Chem., 2005, 26, 313-324.
-
(2005)
J. Sulf. Chem.
, vol.26
, pp. 313-324
-
-
Firouzabadi, H.1
Iranpoor, N.2
Jafarpour, M.3
-
36
-
-
28544434156
-
4 dispersed on dry silica gel provides a useful reagent for S-alkylation of thiols with alcohols under solvent-free conditions
-
DOI 10.1016/j.tetlet.2005.10.137, PII S0040403905023932
-
4 dispersed on dry silica gel provides a useful reagent for S-alkylation of thiols with alcohols under solvent-free conditions. Tetrahedron Lett., 2006, 47, 93-97. (Pubitemid 41743783)
-
(2006)
Tetrahedron Letters
, vol.47
, Issue.1
, pp. 93-97
-
-
Firouzabadi, H.1
Iranpoor, N.2
Jafarpour, M.3
-
37
-
-
33646149375
-
2O as a highly efficient and the moisture tolerant Lewis acid catalyst for Michael addition of amines and indoles to α, β- Unsaturated ketones under solvent-free conditions
-
2O as a highly efficient and the moisture tolerant Lewis acid catalyst for Michael addition of amines and indoles to α, β- unsaturated ketones under solvent-free conditions. J. Mol. Catal. A., 2006, 252, 150-155.
-
(2006)
J. Mol. Catal. A.
, vol.252
, pp. 150-155
-
-
Firouzabadi, H.1
Iranpoor, N.2
Jafarpour, M.3
Ghaderi, A.4
-
39
-
-
0003573091
-
-
th ed. Van Nostrand Reinhold, New York
-
ZrOCl2.8H2O with a rather high LD50 [LD50 [Z1OCl28H2O, oral rat] = 2950 mg/Kg]35 and low toxicity should not be that much harmful to mammalians. It is also a highly water tolerant material, therefore, its handling does not need especial precautions. Lewis, R.J.S.R. Dangerous Properties of Industrial Materials, vol. 3, 8th ed., Van Nostrand Reinhold, New York, 1989.
-
(1989)
Dangerous Properties of Industrial Materials
, vol.3
-
-
Lewis, R.J.S.R.1
|