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Volumn 7, Issue 1, 2010, Pages 32-38

Synthesis of 2,3 and 4,5-dihydro-hydroxy-isoxazoles and isoxazoles under different pH conditions

Author keywords

3 diketoesters; Aryl 1; Dihydro hydroxy isoxazoles; Hydroxylamine; Isoxazoles

Indexed keywords


EID: 77951087903     PISSN: 15701786     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017810790533922     Document Type: Article
Times cited : (9)

References (21)
  • 2
    • 8844285335 scopus 로고    scopus 로고
    • Isoxazole-3-hydroxamic acid derivatives as peptide deformylase inhibitors and potential antibacterial agents
    • DOI 10.1016/j.bmcl.2004.09.087, PII S0960894X04012119
    • Cali, P.; Naerum, L.; Mukhija, S.; Hjelmencrantz, A. Isoxazole-3- hydroxamic acid derivatives as peptide deformylase inhibitors and potential antibacterial agents. Bioorg. Med. Chem. Lett., 2004, 14, 5997. (Pubitemid 39531259)
    • (2004) Bioorganic and Medicinal Chemistry Letters , vol.14 , Issue.24 , pp. 5997-6000
    • Cali, P.1    Naerum, L.2    Mukhija, S.3    Hjelmencrantz, A.4
  • 3
    • 0033618528 scopus 로고    scopus 로고
    • N,N-Dialkylaminosubstituted chromones and isoxazoles as potential anti-inflammatory agents
    • DOI 10.1016/S0014-827X(99)00051-8, PII S0014827X99000518
    • Mazzei, M.; Sottofattori, E.; Dondero, R.; Ibrahim, M.; Melloni, E.; Michetti, M. N, N-Dialkylaminosubstituted chromones and isoxazoles as potential anti-inflammatory agents. Il Farmaco, 1999, 54, 452. (Pubitemid 29405638)
    • (1999) Farmaco , vol.54 , Issue.7 , pp. 452-460
    • Mazzei, M.1    Sottofattori, E.2    Dondero, R.3    Ibrahim, M.4    Melloni, E.5    Michetti, M.6
  • 8
    • 0034609667 scopus 로고    scopus 로고
    • Dipolar cycloaddition of novel 6- (nitrileoxidomethyl) penam sulfone: an efficient route to a new class of p-lactamase inhibitors
    • Sandanayaka, V.P.; Youjun, Y. Dipolar cycloaddition of novel 6- (nitrileoxidomethyl) penam sulfone: an efficient route to a new class of p-lactamase inhibitors. Org. Lett., 2000, 2, 3087.
    • (2000) Org. Lett. , vol.2 , pp. 3087
    • Sandanayaka, V.P.1    Youjun, Y.2
  • 9
    • 34347261691 scopus 로고    scopus 로고
    • Oxidative aromatization of 3,5-disubstituted 2-isoxazolines by nitric oxide
    • Li, R.; Wu, W.T.; Wu, G.L.; Fan, Y.; Wu, L.M. Oxidative aromatization of 3,5-disubstituted 2-isoxazolines by nitric oxide. Chin. Chem. Lett., 2007, 18, 788.
    • (2007) Chin. Chem. Lett. , vol.18 , pp. 788
    • Li, R.1    Wu, W.T.2    Wu, G.L.3    Fan, Y.4    Wu, L.M.5
  • 10
    • 0003025485 scopus 로고    scopus 로고
    • Synthetic Studies of the formation of oxazoles and isoxazoles from N-acetoacetyl derivatives: scope and limitations
    • Lautens, M.; Roy, A. Synthetic Studies of the formation of oxazoles and isoxazoles from N-acetoacetyl derivatives: scope and limitations. Org. Lett., 2000, 2, 555.
    • (2000) Org. Lett. , vol.2 , pp. 555
    • Lautens, M.1    Roy, A.2
  • 11
    • 33846242658 scopus 로고    scopus 로고
    • Isoxazoles from 1,1- disubstituted bromoalkenes
    • Dadiboyena, S.; Xu J.; Hamme, A.T. Isoxazoles from 1,1- disubstituted bromoalkenes. Tetrahedron Lett., 2007, 48, 1295.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 1295
    • Dadiboyena, S.1    Xu, J.2    Hamme, A.T.3
  • 14
    • 0006348882 scopus 로고
    • Asymmetric synthesis of a β-ketol moiety via 3,5- disubstituted isoxazoles: Application to (+)-(S)-[6]-gingerol
    • Baraldi, P.G.; Moroder, F.; Pollini, G.P.; Simoni, D.; Barco, A.; Benetti, S. Asymmetric synthesis of a β-ketol moiety via 3,5- disubstituted isoxazoles: application to (+)-(S)-[6]-gingerol. J. Chem. Soc. Perkin Trans. 1, 1982, 2983.
    • (1982) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 2983
    • Baraldi, P.G.1    Moroder, F.2    Pollini, G.P.3    Simoni, D.4    Barco, A.5    Benetti, S.6
  • 15
    • 0027363856 scopus 로고
    • Regioselective syntheses of 3-aminomethyl-5-substituted isoxazoles: A facile and chemoselective reduction of azide to amino by sodium borohydride using 1,3-propanedithiol as a catalyst
    • DOI 10.1016/S0040-4039(00)60386-6
    • Pei, Y.; Wickham B.O.S. Regioselective syntheses of 3- aminomethyl-5-substituted isoxazoles: a facile and chemoselective reduction of azide to amine by sodium borohydride using 1,3- propanedithiol as a catalyst. Tetrahedron Lett., 1993, 34, 7509. (Pubitemid 23356227)
    • (1993) Tetrahedron Letters , vol.34 , Issue.47 , pp. 7509-7512
    • Pei, Y.1    Wickhan, B.O.S.2
  • 16
    • 0039851319 scopus 로고
    • Synthesis of optically active oxazolines from optically active epoxides
    • Manning, D.T.; Coleman, H.A. Synthesis of optically active oxazolines from optically active epoxides. J. Org. Chem., 1969, 34, 3248.
    • (1969) J. Org. Chem. , vol.34 , pp. 3248
    • Manning, D.T.1    Coleman, H.A.2
  • 17
    • 77951045532 scopus 로고    scopus 로고
    • Cristallographic data for compound 6 have been deposited with the Cambridge Crystallographic Data Centre, No CCDC 718416. Copies of the data can be obtained, free of charge, on application to CCDC (e-mail: deposit@ccdc.cam.ac.uk)
    • Cristallographic data for compound 6 have been deposited with the Cambridge Crystallographic Data Centre, No CCDC 718416. Copies of the data can be obtained, free of charge, on application to CCDC (e-mail: deposit@ccdc.cam.ac.uk).
  • 18
    • 0035847277 scopus 로고    scopus 로고
    • Polysaccharide-based chiral stationary phases for high-performance liquid chromatographic enantioseparation
    • DOI 10.1016/S0021-9673(00)00501-X, PII S002196730000501X
    • Yashima, E. Polysaccharide-based chiral stationary phases for high-performance liquid chromatographic enantioseparation. J. Chromatogr. A., 2001, 906, 105. (Pubitemid 32056199)
    • (2001) Journal of Chromatography A , vol.906 , Issue.1-2 , pp. 105-125
    • Yashima, E.1
  • 19
    • 57349102450 scopus 로고    scopus 로고
    • LC using two different cellulose chiral stationary phases for direct enantioseparation of benzoxazolinone aminoalcohols and aminoketones
    • Lipka, E.; Bonte, J.P.; Vaccher, C. LC using two different cellulose chiral stationary phases for direct enantioseparation of benzoxazolinone aminoalcohols and aminoketones. Chromatographia, 2008, 68, 1053.
    • (2008) Chromatographia , vol.68 , pp. 1053
    • Lipka, E.1    Bonte, J.P.2    Vaccher, C.3
  • 20
    • 36348988451 scopus 로고    scopus 로고
    • Chiral resolution of six melatoninergic ligands, by electrokinetic chromatography using highly sulfated cyclodextrins
    • Lipka, E.; Danel, C.; Orhan, H.; Bonte, J.P.; Vaccher, C. Chiral resolution of six melatoninergic ligands, by electrokinetic chromatography using highly sulfated cyclodextrins. Electrophoresis, 2007, 28, 3915.
    • (2007) Electrophoresis , vol.28 , pp. 3915
    • Lipka, E.1    Danel, C.2    Orhan, H.3    Bonte, J.P.4    Vaccher, C.5
  • 21
    • 27644539385 scopus 로고    scopus 로고
    • Chiral capillary electrophoretic determination of the enantiomeric purity of tetrahydronaphthalenic derivatives, melatoninergic ligands, using highly sulfated β-cyclodextrins
    • Danel, C.; Lipka, E.; Bonte, J.P.; Goossens, J.F.; Vaccher, C.; Foulon, C. Chiral capillary electrophoretic determination of the enantiomeric purity of tetrahydronaphthalenic derivatives, melatoninergic ligands, using highly sulfated β-cyclodextrins. Electrophoresis, 2005, 28, 3824.
    • (2005) Electrophoresis , vol.28 , pp. 3824
    • Danel, C.1    Lipka, E.2    Bonte, J.P.3    Goossens, J.F.4    Vaccher, C.5    Foulon, C.6


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