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1
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0037366617
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For the general review on Baylis-Hillman chemistry, see:
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For the general review on Baylis-Hillman chemistry, see:. Basavaiah D., Rao A.J., and Satyanarayana T. Chem. Rev. 103 (2003) 811-891
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Basavaiah, D.1
Rao, A.J.2
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and further references cited therein
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Singh V., and Batra S. Tetrahedron 64 (2008) 4511-4574 and further references cited therein
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Tetrahedron
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Singh, V.1
Batra, S.2
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5
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33845221323
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For the synthesis of quinolone derivatives from Baylis-Hillman adducts by other groups, see:
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For the synthesis of quinolone derivatives from Baylis-Hillman adducts by other groups, see:. Pathak R., Madapa S., and Batra S. Tetrahedron 63 (2007) 451-460
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(2007)
Tetrahedron
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, pp. 451-460
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Pathak, R.1
Madapa, S.2
Batra, S.3
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6
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43449119537
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Benakki H., Colacino E., Andre C., Guenoun F., Martinez J., and Lamaty F. Tetrahedron 64 (2008) 5949-5955
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(2008)
Tetrahedron
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Benakki, H.1
Colacino, E.2
Andre, C.3
Guenoun, F.4
Martinez, J.5
Lamaty, F.6
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7
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33750152486
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Familoni O.B., Klaas P.J., Lobb K.A., Pakade V.E., and Kaye P.T. Org. Biomol. Chem. 4 (2006) 3960-3965
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Org. Biomol. Chem.
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Familoni, O.B.1
Klaas, P.J.2
Lobb, K.A.3
Pakade, V.E.4
Kaye, P.T.5
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12
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12444337517
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For the synthesis of quinolone derivatives from Baylis-Hillman adducts in our group, see:
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For the synthesis of quinolone derivatives from Baylis-Hillman adducts in our group, see:. Lee C.G., Lee K.Y., Lee S., and Kim J.N. Tetrahedron 61 (2005) 1493-1499
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(2005)
Tetrahedron
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Lee, C.G.1
Lee, K.Y.2
Lee, S.3
Kim, J.N.4
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17
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1542268922
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For the synthesis and biological activities of quinolinone and related compounds, see:
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For the synthesis and biological activities of quinolinone and related compounds, see:. Park K.K., and Lee J.J. Tetrahedron 60 (2004) 2993-2999
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(2004)
Tetrahedron
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Park, K.K.1
Lee, J.J.2
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34547172102
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Battistuzzi G., Bernini R., Cacchi S., Salve I.D., and Fabrizi G. Adv. Synth. Catal. 349 (2007) 297-302
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(2007)
Adv. Synth. Catal.
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Battistuzzi, G.1
Bernini, R.2
Cacchi, S.3
Salve, I.D.4
Fabrizi, G.5
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23
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0031726906
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Huang L.-J., Hsieh M.-C., Teng C.-M., Lee K.-H., and Kuo S.-C. Bioorg. Med. Chem. 6 (1998) 1657-1662
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(1998)
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Huang, L.-J.1
Hsieh, M.-C.2
Teng, C.-M.3
Lee, K.-H.4
Kuo, S.-C.5
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25
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40949111806
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For the Friedel-Crafts reaction with modified Baylis-Hillman adducts, see:
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For the Friedel-Crafts reaction with modified Baylis-Hillman adducts, see:. Lim H.N., Ji S.-H., and Lee K.-J. Synthesis (2007) 2454-2460
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(2007)
Synthesis
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Lim, H.N.1
Ji, S.-H.2
Lee, K.-J.3
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30
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58849165843
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note
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15NO: C, 84.19; H, 5.30; N, 4.91. Found: C, 84.28; H, 5.52; N, 4.63.
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31
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0034637571
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For the coupling reaction with EDC, see:
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For the coupling reaction with EDC, see:. Adam W., Groer P., Humpf H.-U., and Saha-Moller C.R. J. Org. Chem. 65 (2000) 4919-4922
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(2000)
J. Org. Chem.
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Adam, W.1
Groer, P.2
Humpf, H.-U.3
Saha-Moller, C.R.4
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