Indexed keywords
(3,4 DIHYDRO 3,3 DIMETHYLQUINOXALIN 6 YL)PHENYLMETHANONE;
1',4' DIHYDRO 7' METHOXY SPIRO[CYCLOHEXANE 1,2'(3'H)QUINOXALIN]3' ONE;
1,10 PHENANTHROLINE;
1,2 DIHYDRO 2,2 DIMETHYL 7 METHOXYQUINOXALINE;
1,2 DIHYDRO 2,2 DIMETHYLQUINOXALINE;
1,2 DIHYDRO 2,2 DIPHENYL 7 METHOXYQUINOXALINE;
1,2 DIHYDRO 2,2,5 TRIMETHYLQUINOXALINE;
1,2 DIHYDRO 2,2,7 TRIMETHYLQUINOXALINE;
1,2 DIHYDRO 2,2,8 TRIMETHYLQUINOXALINE;
2 PENTYLQUINOXALINE;
2 PENTYLQUINOXALINE 1 OXIDE;
2,2 DIMETHYL 1,2 DIHYDROQUINOXALINE;
3,4 DIHYDRO 3,3 DIMETHYL 2 QUINOXALINONE;
3,4 DIHYDRO 3,3 DIMETHYL 6 METHOXY 2 QUINOXALINONE;
3,4 DIHYDRO 3,3,5 TRIMETHYL 2 QUINOXALINONE;
3,4 DIHYDRO 3,3,8 TRIMETHYL 2 QUINOXALINONE;
6 CHLORO 1,2 DIHYDRO 2,2 DIMETHYLQUINOXALINE;
6 CHLORO 3,4 DIHYDRO 3,3 DIMETHYL 2 QUINOXALINONE;
7 CHLORO 1,2 DIHYDRO 2,2 DIMETHYLQUINOXALINE;
7 CHLORO 2 PHENYLQUINOXALINE;
7 CHLORO 2 PHENYLQUINOXALINE 1 N OXIDE;
7 CHLORO 3,4 DIHYDRO 3,3 DIMETHYL 2 QUINOXALINONE;
7' METHOXY SPIRO[CYCLOHEXANE 1,2'(1'H)QUINOXALINE];
CARBON MONOXIDE;
DIHYDRO 3,3,6 TRIMETHYL 2 QUINOXALINONE;
ENAMINE;
PALLADIUM;
QUINOXALINE DERIVATIVE;
UNCLASSIFIED DRUG;
ANNULATION REACTION;
ARTICLE;
CATALYSIS;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CYCLIZATION;
DRUG SYNTHESIS;
ENVIRONMENTAL TEMPERATURE;
POLYMERIZATION;
PRIORITY JOURNAL;
1
49849097687
For reviews, see:
For reviews, see:
2
33747092660
Ragaini F., Cenini S., Gallo E., Caselli A., and Fantauzzi S. Curr. Org. Chem. 10 (2006) 1479-1510
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Ragaini, F.1
Cenini, S.2
Gallo, E.3
Caselli, A.4
Fantauzzi, S.5
4
41349094803
For a recent application and references, see:
For a recent application and references, see:. Söderberg B.C.G., Banini S.R., Turner M.R., Minter A.R., and Arrington A.K. Synthesis (2008) 903-912
(2008)
Synthesis
, pp. 903-912
Söderberg, B.C.G.1
Banini, S.R.2
Turner, M.R.3
Minter, A.R.4
Arrington, A.K.5
7
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Tollari, S.1
Cenini, S.2
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Cassar, L.4
11
0007802333
Watanabe Y., Yamamoto J., Akazome M., Kondo T., and Mitsudo T.-a. J. Org. Chem. 60 (1995) 8328-8329
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Watanabe, Y.1
Yamamoto, J.2
Akazome, M.3
Kondo, T.4
Mitsudo, T.-a.5
18
37049081811
16 catalysts, see:
16 catalysts, see:. Crotti C., Cenini S., Rindone B., Tollari S., and Demartin F. J. Chem. Soc., Chem. Commun. (1986) 784-786
(1986)
J. Chem. Soc., Chem. Commun.
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Cenini, S.2
Rindone, B.3
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Demartin, F.5
19
0033618383
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Nishiyama, Y.1
Maema, R.2
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Hirose, M.4
Sonoda, N.5
20
34547154811
Sanz R., Escribano J., Pedrosa M.R., Aguado R., and Arnaiz F.J. Adv. Synth. Catal. 349 (2007) 713-718
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Escribano, J.2
Pedrosa, M.R.3
Aguado, R.4
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21
0001431068
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Takatsuki, K.2
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Takegami, Y.5
26
0028417338
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Bassoli, A.1
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Farina, F.3
Orlandi, M.4
Rindone, B.5
30
49849095916
For recent reviews, see:
For recent reviews, see:
31
33845292599
Palacios F., Alonso C., Aparicio D., Rubiales G., and de los Santos J.M. Tetrahedron 63 (2006) 523-575
(2006)
Tetrahedron
, vol.63
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Palacios, F.1
Alonso, C.2
Aparicio, D.3
Rubiales, G.4
de los Santos, J.M.5
33
49849096763
note
For a single example of a related selenium-catalyzed reaction under 30 atm of CO forming 2-propylbenzimidazole in 36% yield, see: Ref. 10.
35
20444452906
Davies I.W., Smitrovich J.H., Sidler R., Qu C., Gresham V., and Bazaral C. Tetrahedron 61 (2005) 6425-6437
(2005)
Tetrahedron
, vol.61
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Davies, I.W.1
Smitrovich, J.H.2
Sidler, R.3
Qu, C.4
Gresham, V.5
Bazaral, C.6
36
17744401781
Söderberg B.C.G., Shriver J.A., Cooper S.H., Shrout T.L., Helton E.S., Austin L.R., Odens H.H., Hearn B.M., Jones P.C., Kouadio T.N., Baswell R., Caprara H.J., Meritt M.D., and Mai T.T. Tetrahedron 59 (2003) 8775-8791
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Söderberg, B.C.G.1
Shriver, J.A.2
Cooper, S.H.3
Shrout, T.L.4
Helton, E.S.5
Austin, L.R.6
Odens, H.H.7
Hearn, B.M.8
Jones, P.C.9
Kouadio, T.N.10
Baswell, R.11
Caprara, H.J.12
Meritt, M.D.13
Mai, T.T.14
39
49849091051
note
The enamine rapidly decomposes/hydrolyzes and correct analyses could not be obtained.
42
49849099450
Meichsner, C.; Riess, G.; Kleim, J. P.; Roesner, M.; Paessens, A.; Blunck, M. Eur. Pat. Appl. EP657166, 1995;
Meichsner, C.; Riess, G.; Kleim, J. P.; Roesner, M.; Paessens, A.; Blunck, M. Eur. Pat. Appl. EP657166, 1995;
43
49849101087
Chem. Abstr. 1995, 123, 228218.
Chem. Abstr. 1995, 123, 228218.
44
0030051558
Jacobsen E.J., TenBrink R.E., Stelzer L.S., Belonga K.L., Carter D.B., Im H.K., Im W.B., Sethy V.H., Tang A.H., VonVoigtlander F.P., and Petke J.D. J. Med. Chem. 39 (1996) 158-175
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Belonga, K.L.4
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Im, H.K.6
Im, W.B.7
Sethy, V.H.8
Tang, A.H.9
VonVoigtlander, F.P.10
Petke, J.D.11
45
49849096677
Billhardt, U. M.; Roesner, M.; Riess, G.; Winkler, I.; Bender, R. Eur. Pat. Appl. EP509398, 1992;
Billhardt, U. M.; Roesner, M.; Riess, G.; Winkler, I.; Bender, R. Eur. Pat. Appl. EP509398, 1992;
46
49849092939
Chem. Abstr. 1993, 118, 234088.
Chem. Abstr. 1993, 118, 234088.
47
49849085293
note
The compound decomposes and turns dark purple upon standing and a correct elemental analysis could not be obtained.
49
49849094206
note
Although the mp is significantly different form the literature value, the structure of 43 was confirmed by 2D NMR experiments including gHSQC, gHMBC, NOESY, and gCOSY.
51
49849096054
Suzuki, K.; Komatsu, T.; Ina, S.; Fujii, K.; Kojima, J.; Yamana, K. Jpn. Kokai Tokkyo Koho JP4282314, 1992;
Suzuki, K.; Komatsu, T.; Ina, S.; Fujii, K.; Kojima, J.; Yamana, K. Jpn. Kokai Tokkyo Koho JP4282314, 1992;
52
49849091251
Chem. Abstr. 1993, 118, 73688.
Chem. Abstr. 1993, 118, 73688.
53
49849088228
note
Commercially available.
54
1842418391
Issidorides C.H., Atfah M.A., Sabounji J.J., Sidani A.R., and Haddadin M.J. Tetrahedron 34 (1978) 217-221
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Haddadin, M.J.5
56
0031463691
Roth T., Morningstar M.L., Boyer P.L., Hughes S.H., Buckheit Jr. R.W., and Michejda C.J. J. Med. Chem. 40 (1997) 4199-4207
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Buckheit Jr., R.W.5
Michejda, C.J.6
57
0033594337
Visentin S., Amiel P., Fruttero R., Boschi D., Roussel C., Giusta L., Carbone E., and Gasco A. J. Med. Chem. 42 (1999) 1422-1427
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Carbone, E.7
Gasco, A.8