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Volumn 18, Issue 5, 2014, Pages 502-506

Ultrasound-promoted, rapid, green, one-pot synthesis of 2'-aminobenzothiazolomethylnaphthols via a multi-component reaction, catalyzed by heteropolyacid in aqueous media

Author keywords

2 Aminobenzothiazole; Green chemistry; Heteropolyacids; Multi component reaction; Ultrasonic irradiation

Indexed keywords


EID: 84908620469     PISSN: 13196103     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jscs.2011.10.013     Document Type: Article
Times cited : (32)

References (36)
  • 2
    • 72249123528 scopus 로고    scopus 로고
    • PTSA catalyzed simple and green synthesis of benzothiazole derivatives in water
    • Azizi N., Amiri A.K., Baghi R., Bolourtchian M., Hashemi M.M. PTSA catalyzed simple and green synthesis of benzothiazole derivatives in water. Monatsh Chem. 2009, 140:1471-1473.
    • (2009) Monatsh Chem. , vol.140 , pp. 1471-1473
    • Azizi, N.1    Amiri, A.K.2    Baghi, R.3    Bolourtchian, M.4    Hashemi, M.M.5
  • 3
    • 61649107650 scopus 로고    scopus 로고
    • Recent trends in the chemistry of 2-aminobenzothiazoles
    • Bondock S., Fadaly W., Metwally M.A. Recent trends in the chemistry of 2-aminobenzothiazoles. J. Sul. Chem. 2009, 30:74-107.
    • (2009) J. Sul. Chem. , vol.30 , pp. 74-107
    • Bondock, S.1    Fadaly, W.2    Metwally, M.A.3
  • 5
    • 34248150492 scopus 로고    scopus 로고
    • Wells-Dawson type heteropolyacid catalyzed synthesis of quinoxaline derivatives at room temperature
    • Heravi M.M., Bakhtiari K., Bamoharram F.F., Tehrani M.H. Wells-Dawson type heteropolyacid catalyzed synthesis of quinoxaline derivatives at room temperature. Monatsh Chem. 2007, 138:465-467.
    • (2007) Monatsh Chem. , vol.138 , pp. 465-467
    • Heravi, M.M.1    Bakhtiari, K.2    Bamoharram, F.F.3    Tehrani, M.H.4
  • 6
    • 65449165027 scopus 로고    scopus 로고
    • Recent developments in use of heteropolyacids, their salts and polyoxometalates in organic synthesis
    • Heravi M.M., Sadjadi S. Recent developments in use of heteropolyacids, their salts and polyoxometalates in organic synthesis. J. Iran. Chem. Soc. 2009, 6:1-54.
    • (2009) J. Iran. Chem. Soc. , vol.6 , pp. 1-54
    • Heravi, M.M.1    Sadjadi, S.2
  • 8
    • 0000677232 scopus 로고
    • Organic reactions in aqueous media-with a focus on carbon-carbon bond formation
    • Li C.J. Organic reactions in aqueous media-with a focus on carbon-carbon bond formation. Chem. Rev. 1993, 93:2023-2035.
    • (1993) Chem. Rev. , vol.93 , pp. 2023-2035
    • Li, C.J.1
  • 9
    • 24044470646 scopus 로고    scopus 로고
    • Organic reactions in aqueous media with a focus on carbon-carbon bond formations: a decade update
    • Li C.J. Organic reactions in aqueous media with a focus on carbon-carbon bond formations: a decade update. Chem. Rev. 2005, 105:3095-3166.
    • (2005) Chem. Rev. , vol.105 , pp. 3095-3166
    • Li, C.J.1
  • 10
    • 0037405276 scopus 로고    scopus 로고
    • Ultrasound promoted synthesis of 2-aroyl-1,3,5-triaryl-4-carbethoxy-4-cyanocyclohexanols
    • Li J.T., Chen G.F., Yang W.Z., Li T.S. Ultrasound promoted synthesis of 2-aroyl-1,3,5-triaryl-4-carbethoxy-4-cyanocyclohexanols. Ultrason. Sonochem. 2003, 10:123-126.
    • (2003) Ultrason. Sonochem. , vol.10 , pp. 123-126
    • Li, J.T.1    Chen, G.F.2    Yang, W.Z.3    Li, T.S.4
  • 11
    • 33646107336 scopus 로고    scopus 로고
    • Some applications of ultrasound irradiation in organic synthesis
    • Li J.T., Wang S.X., Chen G.F., Li T.S. Some applications of ultrasound irradiation in organic synthesis. Curr. Org. Synth. 2005, 2:415-436.
    • (2005) Curr. Org. Synth. , vol.2 , pp. 415-436
    • Li, J.T.1    Wang, S.X.2    Chen, G.F.3    Li, T.S.4
  • 14
    • 60949084915 scopus 로고    scopus 로고
    • An efficient ultrasound-promoted synthesis of the Baylis-Hillman adducts catalyzed by imidazole and l-proline
    • Mamaghani M., Dastmard S. An efficient ultrasound-promoted synthesis of the Baylis-Hillman adducts catalyzed by imidazole and l-proline. Ultrason. Sonochem. 2009, 16:445-447.
    • (2009) Ultrason. Sonochem. , vol.16 , pp. 445-447
    • Mamaghani, M.1    Dastmard, S.2
  • 16
    • 44249102299 scopus 로고    scopus 로고
    • Synthesis of α-oximinoketones under ultrasound irradiation
    • Mehrabi H. Synthesis of α-oximinoketones under ultrasound irradiation. Ultrason. Sonochem. 2008, 15:279-282.
    • (2008) Ultrason. Sonochem. , vol.15 , pp. 279-282
    • Mehrabi, H.1
  • 17
    • 67649502332 scopus 로고    scopus 로고
    • The role of water in the catalysis on solid heteropolyacids
    • Micek-Ilnicka A. The role of water in the catalysis on solid heteropolyacids. J. Mol. Catal. A: Chem. 2009, 308:1-14.
    • (2009) J. Mol. Catal. A: Chem. , vol.308 , pp. 1-14
    • Micek-Ilnicka, A.1
  • 18
    • 33745787895 scopus 로고    scopus 로고
    • Design of multi-component reactions: from Libraries of compounds to libraries of reactions
    • Mironovo M.A. Design of multi-component reactions: from Libraries of compounds to libraries of reactions. QSAR Comb. Sci. 2006, 25:423-431.
    • (2006) QSAR Comb. Sci. , vol.25 , pp. 423-431
    • Mironovo, M.A.1
  • 19
    • 0014598351 scopus 로고
    • Heterocyclic substituted ureas. I. Immunosuppression and virus inhibition by benzimidazolylureas
    • Paget C.J., Kisner K., Stone R.L., Delong D.C. Heterocyclic substituted ureas. I. Immunosuppression and virus inhibition by benzimidazolylureas. J. Med. Chem. 1969, 12:1010-1015.
    • (1969) J. Med. Chem. , vol.12 , pp. 1010-1015
    • Paget, C.J.1    Kisner, K.2    Stone, R.L.3    Delong, D.C.4
  • 21
    • 0000319935 scopus 로고    scopus 로고
    • Ultrasound in materials chemistry
    • Peters D. Ultrasound in materials chemistry. J. Mater. Chem. 1996, 6:1605-1618.
    • (1996) J. Mater. Chem. , vol.6 , pp. 1605-1618
    • Peters, D.1
  • 22
    • 0346456931 scopus 로고    scopus 로고
    • Multicomponent reactions are accelerated in water
    • Pirrung M.C., Sarma K.D. Multicomponent reactions are accelerated in water. J. Am. Chem. Soc. 2004, 126:444-445.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 444-445
    • Pirrung, M.C.1    Sarma, K.D.2
  • 23
    • 67349259326 scopus 로고    scopus 로고
    • Environmentally friendly sonocatalysis promoted preparation of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-1H-pyrazoles
    • Pizzuti L., Piovesan L.A., Flores A.F.C., Quina F.H., Pereira C.M.P. Environmentally friendly sonocatalysis promoted preparation of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-1H-pyrazoles. Ultrason. Sonochem. 2009, 16:728-731.
    • (2009) Ultrason. Sonochem. , vol.16 , pp. 728-731
    • Pizzuti, L.1    Piovesan, L.A.2    Flores, A.F.C.3    Quina, F.H.4    Pereira, C.M.P.5
  • 24
    • 54149085525 scopus 로고    scopus 로고
    • Ultrasound promoted synthesis of substituted pyrazoles and isoxazoles containing sulphone moiety
    • Saleh T.S., EL-Rahman N.M.A. Ultrasound promoted synthesis of substituted pyrazoles and isoxazoles containing sulphone moiety. Ultrason. Sonochem. 2009, 16:237-242.
    • (2009) Ultrason. Sonochem. , vol.16 , pp. 237-242
    • Saleh, T.S.1    EL-Rahman, N.M.A.2
  • 25
    • 0000399555 scopus 로고
    • Synthesis and antiinflammatory activity of 2-amino- and 2-alkylamino-6-benzothiazoleacetic acids, 4-(2'-benzothiazolylamino)-, 4-(4'-substituted-2-thiazolylamino)- and 4-(4'-substituted-3'-alkyl-DELTA.4'-thiazoline-2'-imino)phenylacetic acids
    • Sawhney S.N., Arora S.K., Singh J.V., Bansal O.P., Singh S.P. Synthesis and antiinflammatory activity of 2-amino- and 2-alkylamino-6-benzothiazoleacetic acids, 4-(2'-benzothiazolylamino)-, 4-(4'-substituted-2-thiazolylamino)- and 4-(4'-substituted-3'-alkyl-DELTA.4'-thiazoline-2'-imino)phenylacetic acids. Ind. J. Chem. 1978, 16B:605-609.
    • (1978) Ind. J. Chem. , vol.16 B , pp. 605-609
    • Sawhney, S.N.1    Arora, S.K.2    Singh, J.V.3    Bansal, O.P.4    Singh, S.P.5
  • 26
    • 34748857535 scopus 로고    scopus 로고
    • Clean Synthesis in water: uncatalyzed three-component condensation reaction of 3-amino-1,2,4-triazole or 2-aminobenzimidazole with aldehyde in the presence of activated CH-acids
    • Shabani A., Rahmati A., Rezayan A.H., Darvishi M., Badri Z., Sarvari A. Clean Synthesis in water: uncatalyzed three-component condensation reaction of 3-amino-1,2,4-triazole or 2-aminobenzimidazole with aldehyde in the presence of activated CH-acids. QSAR Comb. Sci. 2007, 26:973-979.
    • (2007) QSAR Comb. Sci. , vol.26 , pp. 973-979
    • Shabani, A.1    Rahmati, A.2    Rezayan, A.H.3    Darvishi, M.4    Badri, Z.5    Sarvari, A.6
  • 27
    • 34548473300 scopus 로고    scopus 로고
    • Water promoted one-pot synthesis of 2'-aminobenzothiazolomethyl naphthols and 5-(2'-aminobenzothiazolomethyl)-6-hydroxyquinolines
    • Shabani A., Rahmati A., Farhangi E. Water promoted one-pot synthesis of 2'-aminobenzothiazolomethyl naphthols and 5-(2'-aminobenzothiazolomethyl)-6-hydroxyquinolines. Tetrahedron Lett. 2007, 48:7291-7294.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 7291-7294
    • Shabani, A.1    Rahmati, A.2    Farhangi, E.3
  • 28
    • 38349158743 scopus 로고    scopus 로고
    • Multicomponent reactions of carbonyl compounds and derivatives of cyanoacetic acid: synthesis of carbo- and heterocycles
    • Shestopalov A.M., Shestopalov A.A., Rodinovskaya L.A. Multicomponent reactions of carbonyl compounds and derivatives of cyanoacetic acid: synthesis of carbo- and heterocycles. Synthesis 2008, 1:11-25.
    • (2008) Synthesis , vol.1 , pp. 11-25
    • Shestopalov, A.M.1    Shestopalov, A.A.2    Rodinovskaya, L.A.3
  • 29
    • 0345893602 scopus 로고
    • Catalyzed by heteropoly compounds. 26. Gas-phase synthesis of methyl tert-butyl ether over heteropolyacids
    • Shikata S., Okuhara T., Misono M. Catalyzed by heteropoly compounds. 26. Gas-phase synthesis of methyl tert-butyl ether over heteropolyacids. J. Mol. Catal. A: Chem. 1995, 100:49-59.
    • (1995) J. Mol. Catal. A: Chem. , vol.100 , pp. 49-59
    • Shikata, S.1    Okuhara, T.2    Misono, M.3
  • 30
    • 33746599078 scopus 로고    scopus 로고
    • Sonochemical nanosynthesis at engineered interface of cavitation microbubble
    • Shchukin D.G., Möhwald H. Sonochemical nanosynthesis at engineered interface of cavitation microbubble. Phys. Chem. Chem. Phys. 2006, 8:3496-3506.
    • (2006) Phys. Chem. Chem. Phys. , vol.8 , pp. 3496-3506
    • Shchukin, D.G.1    Möhwald, H.2
  • 32
    • 70349156384 scopus 로고    scopus 로고
    • Natural product synthesis using multicomponent reaction strategies
    • Touré B.B., Hall D.G. Natural product synthesis using multicomponent reaction strategies. Chem. Rev. 2009, 109:4439-4486.
    • (2009) Chem. Rev. , vol.109 , pp. 4439-4486
    • Touré, B.B.1    Hall, D.G.2
  • 34
    • 0034611437 scopus 로고    scopus 로고
    • Antitumourbenzothiazoles. Part 10: The synthesis and antitumour activity of benzothiazole substituted quinol derivatives
    • Wells G., Bradshaw T.D., Diana P., Seaton A., Shi D.F., Westwell A.D., Stevens M.F.G. Antitumourbenzothiazoles. Part 10: The synthesis and antitumour activity of benzothiazole substituted quinol derivatives. Bioorg. Med. Chem. Lett. 2000, 10:513-515.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 513-515
    • Wells, G.1    Bradshaw, T.D.2    Diana, P.3    Seaton, A.4    Shi, D.F.5    Westwell, A.D.6    Stevens, M.F.G.7
  • 35
    • 58849148311 scopus 로고    scopus 로고
    • Preparation of amidoalkylnaphthols by a three-component reaction catalyzed by 2,4,6-trichloro-1,3,5-triazine under solvent-free conditions
    • Zhang P., Zhang Z.H. Preparation of amidoalkylnaphthols by a three-component reaction catalyzed by 2,4,6-trichloro-1,3,5-triazine under solvent-free conditions. Monatsh Chem. 2009, 140:199-203.
    • (2009) Monatsh Chem. , vol.140 , pp. 199-203
    • Zhang, P.1    Zhang, Z.H.2


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