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MnCl2-promoted synthesis of quinoxaline derivatives at room temperature
被引:38
作者
:
Heravi, Majid M.
论文数:
0
引用数:
0
h-index:
0
机构:
Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran
Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran
Heravi, Majid M.
[
1
]
Bakhtiari, Khadijeh
论文数:
0
引用数:
0
h-index:
0
机构:
Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran
Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran
Bakhtiari, Khadijeh
[
1
]
Oskooie, Hossein A.
论文数:
0
引用数:
0
h-index:
0
机构:
Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran
Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran
Oskooie, Hossein A.
[
1
]
Taheri, Shima
论文数:
0
引用数:
0
h-index:
0
机构:
Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran
Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran
Taheri, Shima
[
1
]
机构
:
[1]
Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran
来源
:
HETEROATOM CHEMISTRY
|
2008年
/ 19卷
/ 02期
关键词
:
D O I
:
10.1002/hc.20401
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
MnCl2 efficiently catalyzes the condensation of o-phenylenediamine derivatives with 1,2-diketones at room temperature to afford the corresponding quinoxaline derivatives in high yields. (C) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:218 / 220
页数:3
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Synthesis and antimicrobial activities of some novel quinoxalinone derivatives
Ali, MM
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Al Azhar Univ, Fac Sci, Dept Chem, Cairo 11884, Egypt
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Ammar, YA
[J].
MOLECULES,
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873
[2]
Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines
Antoniotti, S
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0
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0
h-index:
0
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Univ Nice, UMR CNRS 6001, Lab Aromes Synthese & Interact, Fac Sci, F-06108 Nice 2, France
Antoniotti, S
Duñach, E
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Univ Nice, UMR CNRS 6001, Lab Aromes Synthese & Interact, Fac Sci, F-06108 Nice 2, France
Duñach, E
[J].
TETRAHEDRON LETTERS,
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43
(22)
: 3971
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3973
[3]
An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using molecular iodine as the catalyst
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Dnyanopasak Coll, Organ Chem Synth Lab, Parbhani 431401, Maharashtra, India
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Dnyanopasak Coll, Organ Chem Synth Lab, Parbhani 431401, Maharashtra, India
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[J].
TETRAHEDRON LETTERS,
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46
(42)
: 7183
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7186
[4]
Brock E. D., 1999, [No title captured], Patent No. [WO 9951688, 9951688]
[5]
Brown D. J., 2004, CHEM HETEROCYCLIC CO
[6]
Laterally-extended porphyrin systems incorporating a switchable unit
Crossley, MJ
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Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
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0
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Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
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CHEMICAL COMMUNICATIONS,
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(10)
: 1122
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Dailey S, 2001, J MATER CHEM, V11, P2238, DOI 10.1039/b104674h
[8]
Synthesis of new benzo-substituted macrocyclic ligands containing quinoxaline subunits
Elwahy, AHM
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Cairo Univ, Fac Sci, Dept Chem, Giza, Egypt
Cairo Univ, Fac Sci, Dept Chem, Giza, Egypt
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Bohmer, FD
[J].
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Potent quinoxaline-based inhibitors of PDGF receptor tyrosine kinase activity. Part 2: The synthesis and biological activities of RPR127963 an orally bioavailable inhibitor
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Perrone, MH
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Perrone, MH
[J].
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,
2003,
13
(18)
: 3097
-
3100
←
1
2
3
4
→
共 34 条
[1]
Synthesis and antimicrobial activities of some novel quinoxalinone derivatives
Ali, MM
论文数:
0
引用数:
0
h-index:
0
机构:
Al Azhar Univ, Fac Sci, Dept Chem, Cairo 11884, Egypt
Al Azhar Univ, Fac Sci, Dept Chem, Cairo 11884, Egypt
Ali, MM
Ismail, MMF
论文数:
0
引用数:
0
h-index:
0
机构:
Al Azhar Univ, Fac Sci, Dept Chem, Cairo 11884, Egypt
Ismail, MMF
El-Gaby, MSA
论文数:
0
引用数:
0
h-index:
0
机构:
Al Azhar Univ, Fac Sci, Dept Chem, Cairo 11884, Egypt
El-Gaby, MSA
Zahran, MA
论文数:
0
引用数:
0
h-index:
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机构:
Al Azhar Univ, Fac Sci, Dept Chem, Cairo 11884, Egypt
Zahran, MA
Ammar, YA
论文数:
0
引用数:
0
h-index:
0
机构:
Al Azhar Univ, Fac Sci, Dept Chem, Cairo 11884, Egypt
Ammar, YA
[J].
MOLECULES,
2000,
5
(06)
: 864
-
873
[2]
Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines
Antoniotti, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nice, UMR CNRS 6001, Lab Aromes Synthese & Interact, Fac Sci, F-06108 Nice 2, France
Antoniotti, S
Duñach, E
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nice, UMR CNRS 6001, Lab Aromes Synthese & Interact, Fac Sci, F-06108 Nice 2, France
Duñach, E
[J].
TETRAHEDRON LETTERS,
2002,
43
(22)
: 3971
-
3973
[3]
An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using molecular iodine as the catalyst
Bhosale, RS
论文数:
0
引用数:
0
h-index:
0
机构:
Dnyanopasak Coll, Organ Chem Synth Lab, Parbhani 431401, Maharashtra, India
Bhosale, RS
Sarda, SR
论文数:
0
引用数:
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h-index:
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Sarda, SR
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论文数:
0
引用数:
0
h-index:
0
机构:
Dnyanopasak Coll, Organ Chem Synth Lab, Parbhani 431401, Maharashtra, India
Ardhapure, SS
Jadhav, WN
论文数:
0
引用数:
0
h-index:
0
机构:
Dnyanopasak Coll, Organ Chem Synth Lab, Parbhani 431401, Maharashtra, India
Jadhav, WN
Bhusare, SR
论文数:
0
引用数:
0
h-index:
0
机构:
Dnyanopasak Coll, Organ Chem Synth Lab, Parbhani 431401, Maharashtra, India
Bhusare, SR
Pawar, RP
论文数:
0
引用数:
0
h-index:
0
机构:
Dnyanopasak Coll, Organ Chem Synth Lab, Parbhani 431401, Maharashtra, India
Dnyanopasak Coll, Organ Chem Synth Lab, Parbhani 431401, Maharashtra, India
Pawar, RP
[J].
TETRAHEDRON LETTERS,
2005,
46
(42)
: 7183
-
7186
[4]
Brock E. D., 1999, [No title captured], Patent No. [WO 9951688, 9951688]
[5]
Brown D. J., 2004, CHEM HETEROCYCLIC CO
[6]
Laterally-extended porphyrin systems incorporating a switchable unit
Crossley, MJ
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
Crossley, MJ
Johnston, LA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
Johnston, LA
[J].
CHEMICAL COMMUNICATIONS,
2002,
(10)
: 1122
-
1123
[7]
Dailey S, 2001, J MATER CHEM, V11, P2238, DOI 10.1039/b104674h
[8]
Synthesis of new benzo-substituted macrocyclic ligands containing quinoxaline subunits
Elwahy, AHM
论文数:
0
引用数:
0
h-index:
0
机构:
Cairo Univ, Fac Sci, Dept Chem, Giza, Egypt
Cairo Univ, Fac Sci, Dept Chem, Giza, Egypt
Elwahy, AHM
[J].
TETRAHEDRON,
2000,
56
(06)
: 897
-
907
[9]
Tyrphostins .5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: Structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins
Gazit, A
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,ALEXANDER SILBERMAN INST LIFE SCI,DEPT BIOL CHEM,JERUSALEM,ISRAEL
Gazit, A
App, H
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,ALEXANDER SILBERMAN INST LIFE SCI,DEPT BIOL CHEM,JERUSALEM,ISRAEL
App, H
McMahon, G
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,ALEXANDER SILBERMAN INST LIFE SCI,DEPT BIOL CHEM,JERUSALEM,ISRAEL
McMahon, G
Chen, J
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,ALEXANDER SILBERMAN INST LIFE SCI,DEPT BIOL CHEM,JERUSALEM,ISRAEL
Chen, J
Levitzki, A
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,ALEXANDER SILBERMAN INST LIFE SCI,DEPT BIOL CHEM,JERUSALEM,ISRAEL
Levitzki, A
Bohmer, FD
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,ALEXANDER SILBERMAN INST LIFE SCI,DEPT BIOL CHEM,JERUSALEM,ISRAEL
Bohmer, FD
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1996,
39
(11)
: 2170
-
2177
[10]
Potent quinoxaline-based inhibitors of PDGF receptor tyrosine kinase activity. Part 2: The synthesis and biological activities of RPR127963 an orally bioavailable inhibitor
He, W
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
He, W
Myers, MR
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Myers, MR
Hanney, B
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Hanney, B
Spada, AP
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Spada, AP
Bilder, G
论文数:
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引用数:
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h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Bilder, G
Galzcinski, H
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Galzcinski, H
Amin, D
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Amin, D
Needle, S
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Needle, S
Page, K
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Page, K
Jayyosi, Z
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Jayyosi, Z
Perrone, MH
论文数:
0
引用数:
0
h-index:
0
机构:
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Aventis Pharmaceut, Bridgewater, NJ 08807 USA
Perrone, MH
[J].
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,
2003,
13
(18)
: 3097
-
3100
←
1
2
3
4
→