메뉴 건너뛰기




Volumn 41, Issue 14, 2011, Pages 2103-2114

1-butyl-3-methylimidazolium hydrogen sulfate ([bmim]-HSO 4)-mediated synthesis of polysubstituted quinolines

Author keywords

1 butyl 3 methylimidazolium hydrogen sulfate; 2 aminobenzophenones; bmim HSO4; Ketones; Polysubstituted quinolines

Indexed keywords

1 BUTYL 3 METHYLIMIDAZOLIUM HYDROGEN SULFATE; 2 TERT BUTYL 7 CHLORO 1,2,3,4 TETRAHYDRO 9 PHENYLACRIDINE; ACETIC ACID ETHYL ESTER; ACETONITRILE; ALCOHOL; AMINOACETONITRILE; BENZOPHENONE; IMIDAZOLE DERIVATIVE; IONIC LIQUID; QUINOLINE DERIVATIVE; SOLVENT; TERT BUTYL 2 METHYL 4 PHENYLQUINOLIN 3 CARBOXYLATE; UNCLASSIFIED DRUG; WATER;

EID: 79957637664     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397911.2010.497596     Document Type: Article
Times cited : (19)

References (43)
  • 1
    • 0347417134 scopus 로고    scopus 로고
    • Room-temperature ionic liquids: Solvents for synthesis and catalysis
    • Welton, T. Room-temperature ionic liquids: Solvents for synthesis and catalysis. Chem. Rev. 1999, 99, 2071-2084.
    • (1999) Chem. Rev. , vol.99 , pp. 2071-2084
    • Welton, T.1
  • 2
    • 1342268959 scopus 로고    scopus 로고
    • Mannich reaction using acidic ionic liquids as catalysts and solvents
    • Zhao, G.-Y.; Jiang, T.; Gao, H.-X.; Han, B.-X.; Huang, J.; Sun, D.-H. Mannich reaction using acidic ionic liquids as catalysts and solvents. Green Chem. 2004, 6, 75-77. (Pubitemid 38253311)
    • (2004) Green Chemistry , vol.6 , Issue.2 , pp. 75-77
    • Zhao, G.1    Jiang, T.2    Gao, H.3    Han, B.4    Huang, J.5    Sun, D.6
  • 3
    • 8844277654 scopus 로고    scopus 로고
    • Design and synthesis of novel imidazolium-based ionic liquids with a pseudo crown-ether moiety: Diastereomeric interaction of a racemic ionic liquid with enantiopure europium complexes
    • DOI 10.1016/j.tetlet.2004.10.073, PII S0040403904023044
    • Ishida, Y.; Sasaki, D.; Miyauchi, M.; Saigo, K. Design and synthesis of novel imidazolium-based ionic liquids with a pseudo crown-ether moiety: Diastereomeric interaction of a racemic ionic liquid with enantiopure europium complexes. Tetrahedron Lett. 2004, 45, 9455-9459. (Pubitemid 39535499)
    • (2004) Tetrahedron Letters , vol.45 , Issue.51 , pp. 9455-9459
    • Ishida, Y.1    Sasaki, D.2    Miyauchi, H.3    Saigo, K.4
  • 4
    • 0013188175 scopus 로고    scopus 로고
    • Catalysed esterifications in room temperature ionic liquids with acidic counteranion as recyclable reaction media
    • DOI 10.1016/S1566-7367(02)00087-0
    • Fraga-Dubreuil, J.; Bourahla, K.; Rahmouni, M.; Bazureau, J. P.; Hamelin, J. Catalysed esterifications in room temperature ionic liquids with acidic counteranion as recyclable reaction media. Catal. Commun. 2002, 3, 185-190. (Pubitemid 41087726)
    • (2002) Catalysis Communications , vol.3 , Issue.5 , pp. 185-190
    • Fraga-Dubreuil, J.1    Bourahla, K.2    Rahmouni, M.3    Bazureau, J.P.4    Hamelin, J.5
  • 5
    • 10944258867 scopus 로고    scopus 로고
    • 4] ionic liquid: An acid catalyst for improved synthesis of coumarins
    • DOI 10.1016/j.catcom.2004.10.011, PII S1566736704002158
    • 4] ionic liquid: An acid catalyst for improved synthesis of coumarins. Catal. Commun. 2005, 6, 57-60. (Pubitemid 40009313)
    • (2005) Catalysis Communications , vol.6 , Issue.1 , pp. 57-60
    • Singh, V.1    Kaur, S.2    Sapehiyia, V.3    Singh, J.4    Kad, G.L.5
  • 6
    • 34447573702 scopus 로고    scopus 로고
    • 4: An efficient catalyst for acetalization and thioacetalization of carbonyl compounds and their subsequent deprotection
    • DOI 10.1016/j.catcom.2006.11.030, PII S1566736706004626
    • 4: An efficient catalyst for acetalization and thioacetalization of carbonyl compounds and their subsequent deprotection. Catal. Commun. 2007, 8, 1323-1328. (Pubitemid 47077932)
    • (2007) Catalysis Communications , vol.8 , Issue.9 , pp. 1323-1328
    • Gupta, N.1    Sonu2    Kad, G.L.3    Singh, J.4
  • 7
    • 35848952952 scopus 로고    scopus 로고
    • Brönsted acidic ionic liquid as an efficient catalyst for chemoselective synthesis of 1,1-diacetates under solvent-free conditions
    • DOI 10.1016/j.catcom.2007.05.003, PII S1566736707001860
    • Hajipour, A. R.; Khazdooz, L.; Ruoho, A. E. Brønsted acidic ionic liquid as an efficient catalyst for chemoselective synthesis of 1,1-diacetates under solvent-free conditions. Catal. Commun. 2008, 9, 89-96. (Pubitemid 350061200)
    • (2008) Catalysis Communications , vol.9 , Issue.1 , pp. 89-96
    • Hajipour, A.R.1    Khazdooz, L.2    Ruoho, A.E.3
  • 8
    • 36549010105 scopus 로고    scopus 로고
    • Efficient and eco-friendly synthesis of dihydropyrimidinones, bis(indolyl)methanes, and N-alkyl and N-arylimides in ionic liquids
    • Dabiri, M.; Salehi, P.; Baghbanzadeh, M.; Shakouri, M.; Otokesh, S.; Ekrami, T.; Doosti, R. Efficient and eco-friendly synthesis of dihydropyrimidinones, bis(indolyl)methanes, and N-alkyl and N-arylimides in ionic liquids. J. Iran. Chem. Soc. 2007, 4, 393-401.
    • (2007) J. Iran. Chem. Soc. , vol.4 , pp. 393-401
    • Dabiri, M.1    Salehi, P.2    Baghbanzadeh, M.3    Shakouri, M.4    Otokesh, S.5    Ekrami, T.6    Doosti, R.7
  • 9
    • 65449183418 scopus 로고    scopus 로고
    • Using acidic ionic liquid 1-butyl-3-methylimidazolium hydrogen sulfate in selective nitration of phenols under mild conditions
    • Tajik, H.; Niknam, K.; Parsa, F. Using acidic ionic liquid 1-butyl-3-methylimidazolium hydrogen sulfate in selective nitration of phenols under mild conditions. J. Iran. Chem. Soc. 2009, 6, 159-164;
    • (2009) J. Iran. Chem. Soc. , vol.6 , pp. 159-164
    • Tajik, H.1    Niknam, K.2    Parsa, F.3
  • 11
    • 69549095915 scopus 로고    scopus 로고
    • 4: An efficient reusable acidic ionic liquid for the synthesis of 1,8-dioxo- octahydroxanthenes
    • 4: An efficient reusable acidic ionic liquid for the synthesis of 1,8-dioxo-octahydroxanthenes. J. Chin. Chem. Soc. 2009, 56, 659-665.
    • (2009) J. Chin. Chem. Soc. , vol.56 , pp. 659-665
    • Niknam, K.1    Damya, M.2
  • 12
    • 84944031181 scopus 로고    scopus 로고
    • A. R. Katritzky, C. W. Rees, and E. F. V. Scriven (Eds.); Pergamon: New York
    • Balausubramanian, M.; Keay, J. G. In Comprehensive Heterocyclic Chemistry II; A. R. Katritzky, C. W. Rees, and E. F. V. Scriven (Eds.); Pergamon: New York, 1996; Vol. 5, p. 245.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.5 , pp. 245
    • Balausubramanian, M.1    Keay, J.G.2
  • 13
    • 0034921225 scopus 로고    scopus 로고
    • A novel trifluoromethanesulfonamidophenyl-substituted quinoline derivative GA 0113: Synthesis and pharmacological profiles
    • Morizawa, Y.; Okazoc, T.; Wang, S. Z.; Sasaki, J.; Ebisu, H.; Nishikawa, M.; Shinyyama, H. A novel trifluoromethanesulfonamidophenyl-substituted quinoline derivative, GA 0113: Synthesis and pharmacological profiles. J. Fluorine Chem. 2001, 109, 83.
    • (2001) J. Fluorine Chem. , vol.109 , pp. 83
    • Morizawa, Y.1    Okazoc, T.2    Wang, S.Z.3    Sasaki, J.4    Ebisu, H.5    Nishikawa, M.6    Shinyyama, H.7
  • 14
    • 0033694467 scopus 로고    scopus 로고
    • 1,8-Naphthyridines IV: 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a] [1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities
    • Roma, G.; Braccio, M. D.; Grossi, G.; Mattioli, F.; Ghia, M. 1,8-Naphthyridines IV: 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a] [1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities. Eur. J. Med. Chem. 2000, 35, 1021-1035.
    • (2000) Eur. J. Med. Chem. , vol.35 , pp. 1021-1035
    • Roma, G.1    Braccio, M.D.2    Grossi, G.3    Mattioli, F.4    Ghia, M.5
  • 15
    • 0035811449 scopus 로고    scopus 로고
    • Synthesis and antibacterial evaluation of certain quinolone derivatives
    • Chen, Y. L.; Fang, K. C.; Sheu, J. Y.; Hsu, S. L.; Tzeng, C. C. Synthesis and antibacterial evaluation of certain quinolone derivatives. J. Med. Chem. 2001, 44, 2374-2376.
    • (2001) J. Med. Chem. , vol.44 , pp. 2374-2376
    • Chen, Y.L.1    Fang, K.C.2    Sheu, J.Y.3    Hsu, S.L.4    Tzeng, C.C.5
  • 19
    • 0000226894 scopus 로고    scopus 로고
    • Electrochemical properties and electronic structures of conjugated polyquinolines and polyanthrazolines
    • Agrawal, A. K.; Jenekhe, S. A. Electrochemical properties and electronic structures of conjugated polyquinolines and polyanthrazolines. Chem. Mater. 1996, 8, 579-589; (Pubitemid 126468886)
    • (1996) Chemistry of Materials , vol.8 , Issue.2 , pp. 579-589
    • Agrawal, A.K.1    Jenekhe, S.A.2
  • 20
    • 0035833878 scopus 로고    scopus 로고
    • New conjugated polymers with donor-acceptor architectures: Synthesis and photophysics of carbazole-quinoline and phenothiazine-quinoline copolymers and oligomers exhibiting large intramolecular charge transfer
    • DOI 10.1021/ma0100448
    • Jenekhe, S. A.; Lu, L.; Alam, M. M. M. New conjugated polymers with donor-acceptor architectures: Synthesis and photophysics of carbazole-quinoline and phenothiazinequinoline copolymers and oligomers exhibiting large intramolecular charge transfer. Macromolecules 2001, 34, 7315-7324; (Pubitemid 33025854)
    • (2001) Macromolecules , vol.34 , Issue.21 , pp. 7315-7324
    • Jenekhe, S.A.1    Lu, L.2    Alam, M.M.3
  • 21
    • 0035818622 scopus 로고    scopus 로고
    • Highly fluorescent poly(arylene ethynylene)s containing quinoline and 3-alkylthiophene
    • DOI 10.1021/ma0111562
    • Jégou, G.; Jenekhe, S. A. Highly fluorescent poly(arylene ethynylene)s containing quinoline and 3-alkylthiophene. Macromolecules 2001, 34, 7926-7928. (Pubitemid 33073981)
    • (2001) Macromolecules , vol.34 , Issue.23 , pp. 7926-7928
    • Jegou, G.1    Jenekhe, S.A.2
  • 22
    • 30544453780 scopus 로고    scopus 로고
    • Fused quinolines: Recent synthetic approaches to azoloquinolines: A review
    • Abass, M. Fused quinolines: Recent synthetic approaches to azoloquinolines: A review. Heterocycles 2005, 65, 901-965;
    • (2005) Heterocycles , vol.65 , pp. 901-965
    • Abass, M.1
  • 24
    • 33644539496 scopus 로고    scopus 로고
    • On the mechanism of the Skraup-Doebner-Von Miller quinoline synthesis
    • Denmark, S. E.; Venkatraman, S. On the mechanism of the Skraup-Doebner-Von Miller quinoline synthesis. J. Org. Chem. 2006, 71, 1668-1676.
    • (2006) J. Org. Chem. , vol.71 , pp. 1668-1676
    • Denmark, S.E.1    Venkatraman, S.2
  • 25
    • 0013953457 scopus 로고
    • Friedländer syntheses with o-aminoaryl ketones, I: Acid-catalyzed condensations of o-aminobenzophenone with ketones
    • Fehnel, E. A. Friedländer syntheses with o-aminoaryl ketones, I: Acid-catalyzed condensations of o-aminobenzophenone with ketones. J. Org. Chem. 1966, 31, 2899;
    • (1966) J. Org. Chem. , vol.31 , pp. 2899
    • Fehnel, E.A.1
  • 26
    • 0037462413 scopus 로고    scopus 로고
    • Highly regioselective Friedlä nder annulations with unmodified ketones employing novel amine catalysts: Syntheses of 2-substituted quinolines, 1,8-naphthyridines, and related heterocycles
    • Dormer, P. G.; Eng, K. K.; Farr, R. N.; Hamphrey, G. R.; McWilliams, J. C.; Reider, P. J.; Sager, J. W.; Volante, R. P. Highly regioselective Friedlä nder annulations with unmodified ketones employing novel amine catalysts: Syntheses of 2-substituted quinolines, 1,8-naphthyridines, and related heterocycles. J. Org. Chem. 2003, 68, 467.
    • (2003) J. Org. Chem. , vol.68 , pp. 467
    • Dormer, P.G.1    Eng, K.K.2    Farr, R.N.3    Hamphrey, G.R.4    McWilliams, J.C.5    Reider, P.J.6    Sager, J.W.7    Volante, R.P.8
  • 27
    • 24944461938 scopus 로고    scopus 로고
    • Sulfamic acid: An efficient, cost-effective and recyclable solid acid catalyst for the Friedlander quinoline synthesis
    • DOI 10.1016/j.tetlet.2005.08.042, PII S0040403905017776
    • Yadav, J. S.; Rao, P. P.; Sreenu, D.; Rao, R. S.; Kumar, V. N.; Nagaiah, K.; Prasad, A. R. Sulfamic acid: An efficient, cost-effective, and recyclable solid acid catalyst for the Friedlander quinoline synthesis. Tetrahedron Lett. 2005, 46, 7249-7253. (Pubitemid 41317118)
    • (2005) Tetrahedron Letters , vol.46 , Issue.42 , pp. 7249-7253
    • Yadav, J.S.1    Purushothama Rao, P.2    Sreenu, D.3    Srinivasa Rao, R.4    Naveen Kumar, V.5    Nagaiah, K.6    Prasad, A.R.7
  • 28
    • 0037287085 scopus 로고    scopus 로고
    • A new green approach to the Friedländer synthesis of quinolines
    • Arcadi, A.; Chiarini, M.; Di Giuseppe, S.; Marinelli, F. A new green approach to the Friedländer synthesis of quinolines. Synlett 2003, 203-206; (Pubitemid 36249937)
    • (2003) Synlett , Issue.2 , pp. 203-206
    • Arcadi, A.1    Chiarini, M.2    Di Giuseppe, S.3    Marinelli, F.4
  • 29
    • 13744257781 scopus 로고    scopus 로고
    • A mild and efficient one-step synthesis of quinolines
    • DOI 10.1016/j.tetlet.2005.01.075
    • De, S. K.; Gibbs, R. A. A mild and efficient one-step synthesis of quinolines. Tetrahedron Lett. 2005, 46, 1647-1649; (Pubitemid 40238681)
    • (2005) Tetrahedron Letters , vol.46 , Issue.10 , pp. 1647-1649
    • De, S.K.1    Gibbs, R.A.2
  • 30
    • 27444436217 scopus 로고    scopus 로고
    • 2
    • DOI 10.1055/s-2005-917111, W01605ST
    • 2. Synlett 2005, 2653-2657; (Pubitemid 41532189)
    • (2005) Synlett , Issue.17 , pp. 2653-2657
    • Wu, J.1    Zhang, L.2    Diao, T.-N.3
  • 31
    • 29544442040 scopus 로고    scopus 로고
    • An efficient, high yielding protocol for the synthesis of functionalized quinolines via the tandem addition/annulation reaction of o-aminoaryl ketones with α-methylene ketones
    • DOI 10.1016/j.tetlet.2005.11.075, PII S0040403905025426
    • Bose, D. S.; Kumar, R. K. An efficient, high-yielding protocol for the synthesis of functionalized quinolines via the tandem addition/annulation reaction of o-aminoaryl ketone with a-methylene ketones. Tetrahedron Lett. 2006, 47, 813-816. (Pubitemid 43014817)
    • (2006) Tetrahedron Letters , vol.47 , Issue.5 , pp. 813-816
    • Bose, D.S.1    Kumar, R.K.2
  • 32
    • 5644263760 scopus 로고    scopus 로고
    • Silver phosphotungstate: A novel and recyclable heteropoly acid for Friedländer quinoline synthesis
    • DOI 10.1055/s-2004-831185
    • Yadav, J. S.; Reddy, B. V. S.; Premlatha, P.; Rao, R. S.; Nagaiah, K. Silver phosphotungstate: A novel and recyclable heteropoly acid for Friedländer quinoline synthesis. Synthesis 2004, 2381-2385. (Pubitemid 39371668)
    • (2004) Synthesis , Issue.14 , pp. 2381-2385
    • Yadav, J.S.1    Reddy, B.V.S.2    Sreedhar, P.3    Rao, R.S.4    Nagaiah, K.5
  • 33
    • 34548615698 scopus 로고    scopus 로고
    • Iodine-catalyzed Friedländer quinoline synthesis under solvent-free conditions
    • Zolfigol, M. A.; Salehi, P.; Ghaderia, A.; Shiria, M. Iodine-catalyzed Friedländer quinoline synthesis under solvent-free conditions. J. Chin. Chem. Soc. 2007, 54, 267-271.
    • (2007) J. Chin. Chem. Soc. , vol.54 , pp. 267-271
    • Zolfigol, M.A.1    Salehi, P.2    Ghaderia, A.3    Shiria, M.4
  • 34
    • 34547397908 scopus 로고    scopus 로고
    • Application of heterogeneous solid acid catalysts for Friedlander synthesis of quinolines
    • DOI 10.1016/j.molcata.2007.04.034, PII S1381116907003135
    • Das, B.; Damodar, K.; Chowdhury, N.; Kumar, R. A. Application of heterogeneous solid acid catalysts for Friedländer synthesis of quinolines. J. Mol. Catal. A: Chem. 2007, 274, 148-152. (Pubitemid 47176454)
    • (2007) Journal of Molecular Catalysis A: Chemical , vol.274 , Issue.1-2 , pp. 148-152
    • Das, B.1    Damodar, K.2    Chowdhury, N.3    Kumar, R.A.4
  • 35
    • 34547775111 scopus 로고    scopus 로고
    • A recyclable palladium-catalyzed modified Friedländer quinoline synthesis
    • Cho, C. S.; Ren, W. X. A recyclable palladium-catalyzed modified Friedländer quinoline synthesis. J. Organometal. Chem. 2007, 692, 4182.
    • (2007) J. Organometal. Chem. , vol.692 , pp. 4182
    • Cho, C.S.1    Ren, W.X.2
  • 37
    • 84882754417 scopus 로고    scopus 로고
    • A highly efficient synthesis of trisubstituted quinolines using sodium hydrogensulfate on silica as a reusable catalyst
    • Desai, U. V.; Mitragotri, S. D.; Thopate, T. S.; Pore, D. M.; Wadgaonkar, P. P. A highly efficient synthesis of trisubstituted quinolines using sodium hydrogensulfate on silica as a reusable catalyst. Arkivoc 2006, 15, 198-204.
    • (2006) Arkivoc , vol.15 , pp. 198-204
    • Desai, U.V.1    Mitragotri, S.D.2    Thopate, T.S.3    Pore, D.M.4    Wadgaonkar, P.P.5
  • 38
    • 63449111648 scopus 로고    scopus 로고
    • Phosphotungstic acid: An efficient, cost-effective, and recyclable catalyst for the synthesis of polysubstituted quinolines
    • Dabiri, M.; Bashiribod, S. Phosphotungstic acid: An efficient, cost-effective, and recyclable catalyst for the synthesis of polysubstituted quinolines. Molecules 2009, 14, 1126-1133.
    • (2009) Molecules , vol.14 , pp. 1126-1133
    • Dabiri, M.1    Bashiribod, S.2
  • 39
    • 10644236353 scopus 로고    scopus 로고
    • 2O Friedlander reaction in ionic liquids
    • DOI 10.1139/v04-066
    • Wang, J.; Fan, X.; Zhang, X.; Han Can, L. Green preparation of quinoline derivatives through FeCl3-6H2O-catalyzed Friedländer reaction in ionic liquids. Can. J. Chem. 2004, 82, 1192-1196; (Pubitemid 39647954)
    • (2004) Canadian Journal of Chemistry , vol.82 , Issue.7 , pp. 1192-1196
    • Wang, J.1    Fan, X.2    Zhang, X.3    Han, L.4
  • 40
    • 0344391969 scopus 로고    scopus 로고
    • Ionic liquid-promoted regiospecific Friedlä nder annulation: Novel synthesis of quinolines and fused polycyclic quinolines
    • Palimkar, S. S.; Siddiqui, S. A.; Daniel, T.; Lahoti, R. J.; Srinivasan, J. V. Ionic liquid-promoted regiospecific Friedlä nder annulation: Novel synthesis of quinolines and fused polycyclic quinolines. J. Org. Chem. 2003, 68, 9371-9376;
    • (2003) J. Org. Chem. , vol.68 , pp. 9371-9376
    • Palimkar, S.S.1    Siddiqui, S.A.2    Daniel, T.3    Lahoti, R.J.4    Srinivasan, J.V.5
  • 41
    • 12144260538 scopus 로고    scopus 로고
    • A mild, efficient, and improved protocol for the Friedlä nder synthesis of quinolines using Lewis acidic ionic liquid
    • Karthikeyan, G.; Perumal, P. T. A mild, efficient, and improved protocol for the Friedlä nder synthesis of quinolines using Lewis acidic ionic liquid. J. Heterocycl. Chem. 2004, 41, 1039-1042.
    • (2004) J. Heterocycl. Chem. , vol.41 , pp. 1039-1042
    • Karthikeyan, G.1    Perumal, P.T.2
  • 42
    • 68949097633 scopus 로고    scopus 로고
    • Efficient Friedlander synthesis of quinoline derivatives from 2-aminoarylketones and carbonyl compounds mediated by recyclable PEG-supported sulfonic acid
    • Zhang, X. L.; Wang, Q. Y.; Sheng, S. R.; Wang, Q.; Liu, X. L. Efficient Friedlander synthesis of quinoline derivatives from 2-aminoarylketones and carbonyl compounds mediated by recyclable PEG-supported sulfonic acid. Synth. Commun. 2009, 39, 3293-3304.
    • (2009) Synth. Commun. , vol.39 , pp. 3293-3304
    • Zhang, X.L.1    Wang, Q.Y.2    Sheng, S.R.3    Wang, Q.4    Liu, X.L.5
  • 43
    • 57549083783 scopus 로고    scopus 로고
    • Friedlander synthesis of poly-substituted quinolines in the presence of dodecylphosphonic acid (DPA) as a highly efficient, recyclable, and novel catalyst in aqueous media and solvent-free conditions
    • Ghassamipour, S.; Sardarian, A. R. Friedlander synthesis of poly-substituted quinolines in the presence of dodecylphosphonic acid (DPA) as a highly efficient, recyclable, and novel catalyst in aqueous media and solvent-free conditions. Tetrahedron Lett. 2009, 50, 514-519.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 514-519
    • Ghassamipour, S.1    Sardarian, A.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.