메뉴 건너뛰기




Volumn 8, Issue 6, 2011, Pages 374-379

Efficient syntheses of new chromone- And chromanequinoline hybrids and their aza-analogs

Author keywords

Bis heterocycles; Chalcones; Flavonoid; Quinoline; Quinolinone

Indexed keywords


EID: 79961050759     PISSN: 15701786     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017811796064494     Document Type: Article
Times cited : (5)

References (49)
  • 2
    • 0020626421 scopus 로고
    • Flavonoids, a class of natural products of high pharmacological potency
    • DOI 10.1016/0006-2952(83)90262-9
    • Havsteen, B. Flavonoids, a class of natural products of high pharmacological potency. Biochem. Pharmacol. 1983, 32(7), 1141-1148. (Pubitemid 13135620)
    • (1983) Biochemical Pharmacology , vol.32 , Issue.7 , pp. 1141-1148
    • Havsteen, B.1
  • 3
    • 0028287637 scopus 로고
    • Protective effect of epicatechin, epicatechin gallate, and quercetin on lipid peroxidation in phospholipid bilayers
    • DOI 10.1006/abbi.1994.1039
    • Terao, J.; Piskula, M.; Yao, Q. Protective Effect of Epicatechin, Epicatechin Gallate, and Quercetin on Lipid Peroxidation in Phospholipid Bilayers. Arch. Biochem. Biophys. 1994, 308(1), 278-284. (Pubitemid 24172634)
    • (1994) Archives of Biochemistry and Biophysics , vol.308 , Issue.1 , pp. 278-284
    • Terao, J.1    Piskula, M.2    Yao, Q.3
  • 4
    • 0345148810 scopus 로고    scopus 로고
    • Quercetin may act as a cytotoxic prooxidant after its metabolic activation to semiquinone and quinoidal product
    • DOI 10.1016/S0891-5849(98)00167-1, PII S0891584998001671
    • Metodiewa, D.; Jaiswal, A. K.; Cenas, N.; Dickancait, E.; Segura-Aguilar, J. Quercetin may act as a cytotoxic prooxidant after its metabolic activation to semiquinone and quinoidal product. Free Radical Biol. Med. 1999, 26(1-2), 107-116. (Pubitemid 29001498)
    • (1998) Free Radical Biology and Medicine , vol.26 , Issue.1-2 , pp. 107-116
    • Metodiewa, D.1    Jaiswal, A.K.2    Cenas, N.3    Dickancaite, E.4    Segura-Aguilar, J.5
  • 8
    • 69249229665 scopus 로고    scopus 로고
    • 3-Hydroxy-2-phenyl-4(1H)-quinolinones as promising biologically active compounds
    • Hradil, P.; Hlavac, J.; Soural, M.; Hajduch, M.; Kolar, M.; Vecerova, R. 3-Hydroxy-2-phenyl-4(1H)-quinolinones as Promising Biologically Active Compounds. Mini Rev. Med. Chem. 2009, 9(6), 696-702.
    • (2009) Mini Rev. Med. Chem , vol.9 , Issue.6 , pp. 696-702
    • Hradil, P.1    Hlavac, J.2    Soural, M.3    Hajduch, M.4    Kolar, M.5    Vecerova, R.6
  • 9
    • 33744937125 scopus 로고    scopus 로고
    • Black, D S., Ed.; Thieme: Stuttgart
    • Larsen, R. D. in: Science of Synthesis; Black, D. S., Ed.; Thieme: Stuttgart, 2005; Vol. 15, p 551.
    • (2005) Science of Synthesis , vol.15 , pp. 551
    • Larsen, R.D.1
  • 10
    • 0032568390 scopus 로고    scopus 로고
    • Antitumor agents. 181. Synthesis and biological evaluation of 6,7,2',3',4'-substituted-1,2,3,4-tetrahydro-2-phenyl-4-quinolones as a new class of antimitotic antitumor agents
    • DOI 10.1021/jm9707479
    • Xia, Y.; Yang, Z.-Y.; Xia, P.; Bastow, K. F.; Tachibana, Y.; Kuo, S.-C.; Hamel, E.; Hackl, T.; Lee, K.-H. Antitumor Agents. 181. Synthesis and Biological Evaluation of 6,7,2',3',4'-Substituted-1,2,3,4-tetrahydro-2-phenyl-4-quinolones as a New Class of Antimitotic Antitumor Agents. J. Med. Chem. 1998, 41(7), 1155-1162. (Pubitemid 28207391)
    • (1998) Journal of Medicinal Chemistry , vol.41 , Issue.7 , pp. 1155-1162
    • Xia, Y.1    Yang, Z.-Y.2    Xia, P.3    Bastow, K.F.4    Tachibana, Y.5    Kuo, S.-C.6    Hamel, E.7    Hackl, T.8    Lee, K.-H.9
  • 11
    • 0028101061 scopus 로고
    • Hypervalent iodine oxidation of 2-aryl-1,2,3,4-tetrahydro-4-quinolones : An easy access to 2-aryl-4-quinolones
    • Prakash, O.; Kumar, D.; Saini, R. K.; Singh, S. P. Hypervalent Iodine Oxidation of 2-Aryl-1,2,3,4-tetrahydro-4-quinolones: An Easy Access to 2-Aryl-4-quinolones. Synth. Commun. 1994, 24(15), 2167-2172. (Pubitemid 24244614)
    • (1994) Synthetic Communications , vol.24 , Issue.15 , pp. 2167-2172
    • Prakash, O.1    Kumar, D.2    Saini, R.K.3    Singh, S.P.4
  • 12
    • 0037048763 scopus 로고    scopus 로고
    • Antiproliferative activities of citrus flavonoids against six human cancer cell lines
    • DOI 10.1021/jf020121d
    • Manthey, J. A.; Guthrie, N. Antiproliferative Activities of Citrus Flavonoids against Six Human Cancer Cell Lines. J. Agr. Food Chem. 2002, 50(21), 5837-5843. (Pubitemid 35155302)
    • (2002) Journal of Agricultural and Food Chemistry , vol.50 , Issue.21 , pp. 5837-5843
    • Manthey, J.A.1    Guthrie, N.2
  • 13
    • 4644288455 scopus 로고    scopus 로고
    • An efficient oxidation of 2-aryl-1,2,3,4-tetrahydro-4-quinolones employing ferric chloride hexahydrate-methanol: Synthesis of naturally occurring 4-alkoxy-2-arylquinolines
    • DOI 10.1016/j.tetlet.2004.08.144, PII S0040403904018751
    • Kumar, K. H.; Muralidharan, D.; Perumal, P. T. An efficient oxidation of 2-aryl-1,2,3,4-tetrahydro-4-quinolones employing ferric chloride hexahydrate-methanol: synthesis of naturally occurring 4-alkoxy-2- arylquinolines. Tetrahedron Lett. 2004, 45(42), 7903-7906. (Pubitemid 39296492)
    • (2004) Tetrahedron Letters , vol.45 , Issue.42 , pp. 7903-7906
    • Kumar, K.H.1    Muralidharan, D.2    Perumal, P.T.3
  • 14
    • 33750522019 scopus 로고    scopus 로고
    • Synthesis and Characterization of [1]Benzopyrano[4,3-d][1,3] benzooxazocin-13-one and its Derivatives
    • Wang, J.-F.; Liao, Y.-X.; Kuo, P.-Y.; Gau, Y.-H.; Yang, D.-Y. Synthesis and Characterization of [1]Benzopyrano[4,3-d][1,3]benzooxazocin-13-one and its Derivatives. Synlett 2006, (17), 2791-2795.
    • (2006) Synlett , Issue.17 , pp. 2791-2795
    • Wang, J.-F.1    Liao, Y.-X.2    Kuo, P.-Y.3    Gau, Y.-H.4    Yang, D.-Y.5
  • 15
    • 65249124147 scopus 로고    scopus 로고
    • Preparation of two sets of 5,6,7-trioxygenated dihydroflavonol derivatives as free radical scavengers and neuronal cell protectors to oxidative damage
    • Gong, J.; Huang, K.; Wang, F.; Yang, L.; Feng, Y.; Li, H.; Li, X.; Zeng, S.; Wu, X.; Stoeckigt, J.; Zhao, Y.; Qu, J. Preparation of two sets of 5,6,7-trioxygenated dihydroflavonol derivatives as free radical scavengers and neuronal cell protectors to oxidative damage. Bioorg. Med. Chem. 2009, 17(9), 3414-3425.
    • (2009) Bioorg. Med. Chem , vol.17 , Issue.9 , pp. 3414-3425
    • Gong, J.1    Huang, K.2    Wang, F.3    Yang, L.4    Feng, Y.5    Li, H.6    Li, X.7    Zeng, S.8    Wu, X.9    Stoeckigt, J.10    Zhao, Y.11    Qu, J.12
  • 17
    • 60549083759 scopus 로고    scopus 로고
    • Dual Excited-State Intramolecular Proton Transfer Reaction in 3-Hydroxy-2-(pyridin-2-yl)-4H-chromen-4-one
    • Chen, C.-L.; Lin, C.-W.; Hsieh, C.-C.; Lai, C.-H.; Lee, G.-H.; Wang, C.-C.; Chou, P.-T. Dual Excited-State Intramolecular Proton Transfer Reaction in 3-Hydroxy-2-(pyridin-2-yl)-4H-chromen-4-one. J. Phys. Chem. A 2009, 113(1), 205-214.
    • (2009) J. Phys. Chem. A , vol.113 , Issue.1 , pp. 205-214
    • Chen, C.-L.1    Lin, C.-W.2    Hsieh, C.-C.3    Lai, C.-H.4    Lee, G.-H.5    Wang, C.-C.6    Chou, P.-T.7
  • 18
    • 36249008520 scopus 로고    scopus 로고
    • Diels-Alder adducts from flavonoid
    • DOI 10.1016/j.tetlet.2007.08.137, PII S0040403907020618
    • Laroche, M.-F.; Marchand, A.; Duflos, A.; Massiot, G. Diels-Alder adducts from flavonoid. Tetrahedron Lett. 2007, 48(51), 9056-9058. (Pubitemid 350130266)
    • (2007) Tetrahedron Letters , vol.48 , Issue.51 , pp. 9056-9058
    • Laroche, M.-F.1    Marchand, A.2    Duflos, A.3    Massiot, G.4
  • 20
    • 61349195227 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of some new 2,3-dimethoxy-3-hydroxy- 2-(1-phenyl-3-aryl-4-pyrazolyl)chromanones
    • Prakash, O.; Kumar, R.; Sehrawat, R. Synthesis and antibacterial activity of some new 2,3-dimethoxy-3-hydroxy-2-(1-phenyl-3-aryl-4-pyrazolyl)chromanones. Eur. J. Med. Chem. 2009, 44(4), 1763-1767.
    • (2009) Eur. J. Med. Chem , vol.44 , Issue.4 , pp. 1763-1767
    • Prakash, O.1    Kumar, R.2    Sehrawat, R.3
  • 21
    • 57349148119 scopus 로고    scopus 로고
    • Efficient synthesis of chromone and flavonoid derivatives with diverse heterocyclic units
    • Arai, M. A.; Sato, M.; Sawada, K.; Hosoya, T.; Ishibashi, M. Efficient Synthesis of Chromone and Flavonoid Derivatives with Diverse Heterocyclic Units. Chem. Asian J. 2008, 3(12),2056-2064.
    • (2008) Chem. Asian J , vol.3 , Issue.12 , pp. 2056-2064
    • Arai, M.A.1    Sato, M.2    Sawada, K.3    Hosoya, T.4    Ishibashi, M.5
  • 22
    • 70349689996 scopus 로고    scopus 로고
    • Epothilone Analogues with Benzimidazole and Quinoline Side Chains: Chemical synthesis, antiproliferative activity, and interactions with tubulin
    • Dietrich, S. A.; Lindauer, R.; Stierlin, C.; Gertsch, J.; Matesanz, R.; Notararigo, S.; Diaz, J. F.; Altmann, K.-H. Epothilone Analogues with Benzimidazole and Quinoline Side Chains: Chemical Synthesis, Antiproliferative Activity, and Interactions with Tubulin. Chem. Eur. J. 2009, 15(39), 10144-10157.
    • (2009) Chem. Eur. J , vol.15 , Issue.39 , pp. 10144-10157
    • Dietrich, S.A.1    Lindauer, R.2    Stierlin, C.3    Gertsch, J.4    Matesanz, R.5    Notararigo, S.6    Diaz, J.F.7    Altmann, K.-H.8
  • 24
    • 67650482800 scopus 로고    scopus 로고
    • Synthesis and analysis of potential DNA intercalators containing quinoline-glucose hybrids
    • Wei, L.; Zhang, Z.-W.; Wang, S.-X.; Ren, S.-M.; Jiang, T. Synthesis and Analysis of Potential DNA Intercalators Containing Quinoline-Glucose Hybrids. Chem. Biol. Drug Des. 2009, 74(1), 80-86.
    • (2009) Chem. Biol. Drug Des , vol.74 , Issue.1 , pp. 80-86
    • Wei, L.1    Zhang, Z.-W.2    Wang, S.-X.3    Ren, S.-M.4    Jiang, T.5
  • 26
    • 67349171068 scopus 로고    scopus 로고
    • Recent developments in the design and synthesis of hybrid molecules basedon aminoquinoline ring and their antiplasmodial evaluation
    • Kouznetsov, V. V.; Gomez-Barrio, A. Recent developments in the design and synthesis of hybrid molecules basedon aminoquinoline ring and their antiplasmodial evaluation. Eur. J. Med. Chem. 2009, 44(8), 3091-3113.
    • (2009) Eur. J. Med. Chem , vol.44 , Issue.8 , pp. 3091-3113
    • Kouznetsov, V.V.1    Gomez-Barrio, A.2
  • 27
    • 1242316919 scopus 로고    scopus 로고
    • Novel quinazoline-quinoline alkaloids with cytotoxic and DNA topoisomerase II inhibitory activities
    • DOI 10.1016/j.bmcl.2003.12.048
    • Ma, Z.; Hano, Y.; Nomura, T.; Chen, Y. Novel quinazoline-quinoline alkaloids with cytotoxic and DNA topoisomerase II inhibitory activities. Bioorg. Med. Chem. Lett. 2004, 14(5), 1193-1196. (Pubitemid 38229854)
    • (2004) Bioorganic and Medicinal Chemistry Letters , vol.14 , Issue.5 , pp. 1193-1196
    • Ma, Z.1    Hano, Y.2    Nomura, T.3    Chen, Y.4
  • 28
    • 0025815488 scopus 로고
    • Peptide leukotrienes: Current status of research
    • Shaw, A.; Krell, K. D. Peptide leukotrienes: current status of research. J. Med. Chem. 1991, 34(4), 1235-1242.
    • (1991) J. Med. Chem , vol.34 , Issue.4 , pp. 1235-1242
    • Shaw, A.1    Krell, K.D.2
  • 29
    • 0035981596 scopus 로고    scopus 로고
    • Synthesis and reactions of some 2-Methyl-4-oxo-4 H -1-benzopyrans and 2-Methyl-4-oxo-4H-1-benzo[b]-thiopheno[3,2-b]pyrans
    • Ibrahim, S. S.; El-Shaaer, H. M.; Hassan, A. Synthesis and Reactions of Some 2-Methyl-4-oxo-4 H -1-benzopyrans and 2-Methyl-4-oxo-4H-1-benzo[b]- thiopheno[3,2-b]pyrans. Phosphorus, Sulfur Silicon Relat. Elem. 2002, 177(1), 151-172.
    • (2002) Phosphorus, Sulfur Silicon Relat. Elem , vol.177 , Issue.1 , pp. 151-172
    • Ibrahim, S.S.1    El-Shaaer, H.M.2    Hassan, A.3
  • 30
    • 68549110382 scopus 로고    scopus 로고
    • Design and Synthesis of 2-(3-Benzo[b]thienyl)-6,7-methylenedioxyquinolin- 4-one Analogues as Potent Antitumor Agents that Inhibit Tubulin Assembly Design and Synthesis of 2-(3-Benzo[b]thienyl)-6,7-methylenedioxyquinolin-4-one Analogues as Potent Antitumor Agents that Inhibit Tubulin Assembly
    • Chang, Y. H.; Hsu, M. H.; Wang, S. H.; Huang, L. J.; Qian, K.; Morris-Natschke, S. L.; Hamel, E. ; Kuo, S. C.; Lee, K. H. Design and Synthesis of 2-(3-Benzo[b]thienyl)-6,7-methylenedioxyquinolin-4-one Analogues as Potent Antitumor Agents that Inhibit Tubulin Assembly Design and Synthesis of 2-(3-Benzo[b]thienyl)-6,7-methylenedioxyquinolin-4-one Analogues as Potent Antitumor Agents that Inhibit Tubulin Assembly. J. Med. Chem. 2009, 52(15), 4883-4891.
    • (2009) J. Med. Chem , vol.52 , Issue.15 , pp. 4883-4891
    • Chang, Y.H.1    Hsu, M.H.2    Wang, S.H.3    Huang, L.J.4    Qian, K.5    Morris-Natschke, S.L.6    Hamel, E.7    Kuo, S.C.8    Lee, K.H.9
  • 31
    • 29144439841 scopus 로고    scopus 로고
    • Efficient synthesis of 3-pyrrolylquinolines via an 1,3-dipolar cycloaddition/oxidation sequence
    • DOI 10.1080/00397910500290425
    • Menasra, H.; Kedjadja, A.; Rhouati, S.; Carboni, B.; Belfaitah, A. Efficient Synthesis of 3-Pyrrolylquinolines via an 1,3-Dipolar Cycloaddition/Oxidation Sequence. Synth. Commun. 2005, 35(21), 2779-2788. (Pubitemid 41800889)
    • (2005) Synthetic Communications , vol.35 , Issue.21 , pp. 2779-2788
    • Menasra, H.1    Kedjadja, A.2    Debache, A.3    Rhouati, S.4    Belfaitah, A.5    Carboni, B.6
  • 33
    • 34147214190 scopus 로고    scopus 로고
    • Ethyl trans-3-(2-chloro-6,7-dimethylquinolin-3-yl)-1-cyclohexylaziridine- 2-carboxylate
    • Bouraiou, A.; Belfaitah, A.; Bouacida, S.; Benard-Rocherulle, P.; Carboni, B. Ethyl trans-3-(2-chloro-6,7-dimethylquinolin-3-yl)-1- cyclohexylaziridine-2-carboxylate. Acta Cryst. 2007, E63, o1626-1628.
    • (2007) Acta Cryst , vol.E63
    • Bouraiou, A.1    Belfaitah, A.2    Bouacida, S.3    Benard-Rocherulle, P.4    Carboni, B.5
  • 34
    • 40949150332 scopus 로고    scopus 로고
    • 1,3-Dipolar cycloaddition of stabilized azomethine ylides to alkenyl quinolines: An efficient route to polyfunctionalized 3-pyrrolidinylquinoline derivatives
    • Bouraiou, A.; Debbache, A.; Rhouati, S.; Carboni, B.; Belfaitah, A. 1,3-Dipolar cycloaddition of stabilized azomethine ylides to alkenyl quinolines: An efficient route to polyfunctionalized 3-pyrrolidinylquinoline derivatives. J. Heterocyclic Chem. 2008, 45(2), 329-333. (Pubitemid 351415374)
    • (2008) Journal of Heterocyclic Chemistry , vol.45 , Issue.2 , pp. 329-333
    • Bouraiou, A.1    Debache, A.2    Rhouati, S.3    Carboni, B.4    Belfaitah, A.5
  • 35
    • 0023764494 scopus 로고
    • 2(1H)-Quinolinones with cardiac stimulant activity.1. Synthesis and biological activities of (six-membered heteroaryl)-substituted derivatives
    • Alabaster, C. T.; Bell, A. S.; Campbell, S. F.; Ellis, P.; Henderson, C. G.; Roberts, D. A.; Ruddock, K. S.; Samuels, G. M. R.; Stefaniak, M. H. 2(1H)-Quinolinones with cardiac stimulant activity. 1. Synthesis and biological activities of (six-membered heteroaryl)-substituted derivatives. J. Med. Chem. 1988, 31(10), 2048-2056.
    • (1988) J. Med. Chem , vol.31 , Issue.10 , pp. 2048-2056
    • Alabaster, C.T.1    Bell, A.S.2    Campbell, S.F.3    Ellis, P.4    Henderson, C.G.5    Roberts, D.A.6    Ruddock, K.S.7    Samuels, G.M.R.8    Stefaniak, M.H.9
  • 37
    • 44549083008 scopus 로고    scopus 로고
    • First total synthesis of (±)-abyssinoflavanone V
    • Yang, J. H.; Zhao, Y. M.; Ji, C. B. First total synthesis of (±)-abyssinoflavanone V. Chin. Chem. Lett. 2008, 19(6), 658-660.
    • (2008) Chin. Chem. Lett , vol.19 , Issue.6 , pp. 658-660
    • Yang, J.H.1    Zhao, Y.M.2    Ji, C.B.3
  • 38
    • 58549104105 scopus 로고    scopus 로고
    • Synthesis biological evaluation and quantitative structure-activities relationship of flavonoids as vasorelaxant agents
    • Dong, X.; Liu, T.; Yan, J.; Wu, P.; Chen, J.; Hu, Y. Synthesis, biological evaluation and quantitative structure-activities relationship of flavonoids as vasorelaxant agents. Bioorg. Med. Chem. 2009, 17(2), 716-726.
    • (2009) Bioorg. Med. Chem , vol.17 , Issue.2 , pp. 716-726
    • Dong, X.1    Liu, T.2    Yan, J.3    Wu, P.4    Chen, J.5    Hu, Y.6
  • 39
    • 0025425581 scopus 로고
    • Microbiological Transformation of (±)-Flavanone and (±)-Isoflavanone
    • Ibrahim, A. S.; Abul-Hajj, Y. J. Microbiological Transformation of (±)-Flavanone and (±)-Isoflavanone. J. Nat. Prod. 1990, 53(3), 644-656.
    • (1990) J. Nat. Prod , vol.53 , Issue.3 , pp. 644-656
    • Ibrahim, A.S.1    Abul-Hajj, Y.J.2
  • 40
    • 71849111943 scopus 로고    scopus 로고
    • Natural and synthetic 2'-hydroxy-chalcones and aurones: Synthesis, characterization and evaluation of the antioxidant and soybean lipoxygenase inhibitory activity
    • Detsi, A.; Majdalani, M.; Kontogiorgis, C.; Hadjipavlou-Litina, D.; Kefalas, P. Natural and synthetic 2'-hydroxy-chalcones and aurones: Synthesis, characterization and evaluation of the antioxidant and soybean lipoxygenase inhibitory activity. Bioorg. Med. Chem. 2009, 17(23), 8073-8085.
    • (2009) Bioorg. Med. Chem , vol.17 , Issue.23 , pp. 8073-8085
    • Detsi, A.1    Majdalani, M.2    Kontogiorgis, C.3    Hadjipavlou-Litina, D.4    Kefalas, P.5
  • 41
    • 0025735909 scopus 로고
    • Cyclisation and subsequent reactions of 2'-hydroxy-6'-methoxychalcone epoxide and related compounds
    • Adams, C. J.; Main, L. Cyclisation and subsequent reactions of 2'-hydroxy-6'-methoxychalcone epoxide and related compounds. Tetrahedon 1991, 47(27), 4979-4990.
    • (1991) Tetrahedon , vol.47 , Issue.27 , pp. 4979-4990
    • Adams, C.J.1    Main, L.2
  • 42
    • 0000647729 scopus 로고    scopus 로고
    • Ring closing and photooxidation in nitrogen analogues of 3-hydroxyflavone
    • Gao, F.; Johnson, K. F.; Schlenoff, J. B. Ring closing and photooxidation in nitrogen analogues of 3-hydroxyflavone. J. Chem. Soc. Perkin Trans. 2 1996, (2), 269-273.
    • (1996) J. Chem. Soc. Perkin Trans. , vol.2 , Issue.2 , pp. 269-273
    • Gao, F.1    Johnson, K.F.2    Schlenoff, J.B.3
  • 43
    • 79961040062 scopus 로고    scopus 로고
    • Crystallographic data (excluding structure factors) for compounds 9b, 10b and 11b have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC786116, CCDC786117, CCDC786115 These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • Crystallographic data (excluding structure factors) for compounds 9b, 10b and 11b have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC786116, CCDC786117, CCDC786115. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 44
    • 0032512029 scopus 로고    scopus 로고
    • Synthesis of optically active 2,3-substituted-1,2,3,4-tetrahydro-4- quinolones using polyleucine
    • DOI 10.1016/S0040-4039(98)01249-0, PII S0040403998012490
    • Chen, W. P.; Egar, A. L.; Hursthouse, M. B.; Abdul Malik, K.M.; Mathews J. E.; Roberts S. M. Synthesis of optically active 2,3-substituted-1,2,3,4- tetrahydro-4-quinolones using polyleucine. Tetrahedron Lett. 1998, 39(46), 8495-8498. (Pubitemid 28505549)
    • (1998) Tetrahedron Letters , vol.39 , Issue.46 , pp. 8495-8498
    • Chen, W.-P.1    Egar, A.L.2    Hursthouse, M.B.3    Malik, K.M.A.4    Mathews, J.E.5    Roberts, S.M.6
  • 45
    • 0345925415 scopus 로고
    • The chemistry of 2'-amino analogs of 2'-hydroxychalcone and its derivatives
    • Donnelly, J. A.; Farrell D. F. The chemistry of 2'-amino analogs of 2'-hydroxychalcone and its derivatives. J. Org. Chem. 1990, 55(6), 1757-1761.
    • (1990) J. Org. Chem , vol.55 , Issue.6 , pp. 1757-1761
    • Donnelly, J.A.1    Farrell, D.F.2
  • 46
    • 0025253724 scopus 로고
    • Chalcone derivatives as precursors of 1,2,3,4-tetrahydro-4-quinolones
    • Donnelly, J. A.; Farrell, D. F. Chalcone derivatives as precursors of 1,2,3,4-tetrahydro-4-quinolones. Tetrahedron 1990, 46(3), 885.
    • (1990) Tetrahedron , vol.46 , Issue.3 , pp. 885
    • Donnelly, J.A.1    Farrell, D.F.2
  • 47
    • 0027322831 scopus 로고
    • Schmidt reaction on 2-aryl-1,2,3,4-tetrahydro-4-quinolone
    • Tokes, A. L.; Litkei, G. Schmidt Reaction on 2-Aryl-1,2,3,4-tetrahydro-4- quinolone. Synth. Commun. 1993, 23(7), 895-902 and references cited therein. (Pubitemid 23137469)
    • (1993) Synthetic Communications , vol.23 , Issue.7 , pp. 895-902
    • Tokes, A.L.1    Litkei, G.2
  • 48
    • 0346057824 scopus 로고    scopus 로고
    • Indium (III) chloride/silica gel-promoted facile and rapid cyclization of 2-aminochalcones to 2-aryl-2,3-dihydroquinolin-4(1H)-ones under solvent-free conditions
    • Hemanth Kumar, K.; Muralidharan, D.; Perumal, P. T. Indium (III) Chloride/Silica Gel-Promoted Facile and Rapid Cyclization of 2-Aminochalcones to 2-Aryl-2,3-dihydroquinolin-4(1H)-ones under Solvent-Free Conditions. Synthesis 2004, (1), 1, 63-69.
    • (2004) Synthesis , vol.1 , Issue.1 , pp. 63-69
    • Hemanth, K.K.1    Muralidharan, D.2    Perumal, P.T.3
  • 49
    • 79961045389 scopus 로고    scopus 로고
    • 2O: 322.0872; found: 322.0864.
    • Note


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.