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Volumn 19, Issue 3, 2012, Pages 475-478

Efficient one-pot three-component synthesis of N-(4-arylthiazol-2-yl) hydrazones in water under ultrasound irradiation

Author keywords

Aqueous media; Condensation; Hydrazothiazole; One pot synthesis; Ultrasound irradiation

Indexed keywords

CONDENSATION; ULTRASONICS;

EID: 84855268821     PISSN: 13504177     EISSN: 18732828     Source Type: Journal    
DOI: 10.1016/j.ultsonch.2011.10.017     Document Type: Article
Times cited : (33)

References (24)
  • 1
    • 0035372002 scopus 로고    scopus 로고
    • Antitumour activity of transition metal complexes with the thiosemicarbazone derived from 3-acetylumbelliferone
    • DOI 10.1023/A:1007159301849
    • M. Wang, L.F. Wang, Y.Z. Li, Q.X. Li, Z.D. Xu, D.M. Qu, Antitumour activity of transition metal complexes with the thiosemicarbazone derived from 3-acetylumbelliferone, Trans. Met. Chem. 26 (2001) 307-310. (Pubitemid 32302078)
    • (2001) Transition Metal Chemistry , vol.26 , Issue.3 , pp. 307-310
    • Wang, M.1    Wang, L.-F.2    Li, Y.-Z.3    Li, Q.-X.4    Xu, Z.-D.5    Qu, D.-M.6
  • 2
    • 0028365057 scopus 로고
    • Synthesis and anti-pseudomonal activity of new 2-isocephems with a dihydroxypyridone moiety at C-7
    • K. Tsuji, H. Ishikawa, Synthesis and anti-pseudomonal activity of new 2- isocephems with a dihydroxypyridone moiety at C-7, Bioorg. Med. Chem. Lett. 4 (1994) 1601-1605.
    • (1994) Bioorg. Med. Chem. Lett. , vol.4 , pp. 1601-1605
    • Tsuji, K.1    Ishikawa, H.2
  • 6
    • 0028850110 scopus 로고
    • Phenethylthiazolethiourea (PETT) compounds a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis, basic structure-activity relationship studies of PETT, analogs
    • F.W. Bell, A.S. Cantrell, M. Hoegberg, S.R. Jaskunas, N.G. Johansson, C.L. Jordan, M.D. Kinnick, P. Lind, J.M. Morin Jr., Phenethylthiazolethiourea (PETT) compounds a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis, basic structure-activity relationship studies of PETT, analogs, J. Med. Chem. 38 (1995) 4929-4936.
    • (1995) J. Med. Chem. , vol.38 , pp. 4929-4936
    • Bell, F.W.1    Cantrell, A.S.2    Hoegberg, M.3    Jaskunas, S.R.4    Johansson, N.G.5    Jordan, C.L.6    Kinnick, M.D.7    Lind, P.8    Morin Jr., J.M.9
  • 7
    • 0033593962 scopus 로고    scopus 로고
    • Syntheses biological activities of bis(3- Indolyl)thiazoles analogues of marine bis(indole)alkaloid nortopsentins
    • (a) X.H. Gu, X.Z. Wan, B. Jiang, Syntheses biological activities of bis(3- indolyl)thiazoles analogues of marine bis(indole)alkaloid nortopsentins, Bioorg. Med. Chem. Lett. 9 (1999) 569-572;
    • (1999) Bioorg. Med. Chem. Lett. , vol.9 , pp. 569-572
    • Gu, X.H.1    Wan, X.Z.2    Jiang, B.3
  • 8
    • 0034000795 scopus 로고    scopus 로고
    • Syntheses cytotoxicity evaluation of bis(indolyl)thiazole bis(indolyl)pyrazinone and bis(indolyl)pyrazine: Analogues of cytotoxic marine bis(indole) alkaloid
    • (b) B. Jiang, X.H. Gu, Syntheses cytotoxicity evaluation of bis(indolyl)thiazole bis(indolyl)pyrazinone and bis(indolyl)pyrazine: analogues of cytotoxic marine bis(indole) alkaloid, Bioorg. Med. Chem. 8 (2000) 363-371;
    • (2000) Bioorg. Med. Chem. , vol.8 , pp. 363-371
    • Jiang, B.1    Gu, X.H.2
  • 9
    • 0027138655 scopus 로고
    • Synthesis of 2,4-disubstituted thiazoles selenazoles as potential antitumor antifilarial agents. 1. Methyl 4-(isothiocyanatomethyl)thiazole-2- carbamates, - Selenazole-2-carbamates and related derivatives
    • (c) Y. Kumar, R. Green, K.Z. Borysko, D.S. Wise, L.L. Wotring, L.B. Townsend, Synthesis of 2,4-disubstituted thiazoles selenazoles as potential antitumor antifilarial agents. 1. Methyl 4-(isothiocyanatomethyl)thiazole-2- carbamates, - selenazole-2-carbamates and related derivatives, J. Med. Chem. 36 (1993) 3843-3848;
    • (1993) J. Med. Chem. , vol.36 , pp. 3843-3848
    • Kumar, Y.1    Green, R.2    Borysko, K.Z.3    Wise, D.S.4    Wotring, L.L.5    Townsend, L.B.6
  • 10
    • 0027133220 scopus 로고
    • Synthesis of 2,4-disubstituted thiazoles and selenazoles as potential antifilarial and antitumor agents. 2. 2-Arylamido and 2-alkylamido derivatives of 2-amino-4-(isothiocyanatomethyl)thiazole and 2-amino-4- (isothiocyanatomethyl)selenazole
    • DOI 10.1021/jm00076a013
    • (d) Y. Kumar, R. Green, D.S. Wise, L.L. Wotring, L.B. Townsend, Synthesis of 2,4- disubstituted thiazoles selenazoles as potential antifilarial antitumor agents. 2. 2-Arylamido, 2-alkylamido derivatives of 2-amino-4- (isothiocyanatomethyl) thiazole 2-amino-4-(isothiocyanatomethyl)selenazole, J. Med. Chem. 36 (1993) 3849-3852. (Pubitemid 24006714)
    • (1993) Journal of Medicinal Chemistry , vol.36 , Issue.24 , pp. 3849-3852
    • Kumar, Y.1    Green, R.2    Wise, D.S.3    Wotring, L.L.4    Townsend, L.B.5
  • 14
    • 0141788008 scopus 로고    scopus 로고
    • An investigation of the biological effect of structural modifications of isothiose micarbazones and their cyclic analogues
    • (d) E. Maccioni, M.C. Cardia, S. Distinto, L. Bonsignore, A. De Logu, An investigation of the biological effect of structural modifications of isothiose micarbazones and their cyclic analogues, Il Farmaco 58 (2003) 951-959;
    • (2003) Il Farmaco , vol.58 , pp. 951-959
    • Maccioni, E.1    Cardia, M.C.2    Distinto, S.3    Bonsignore, L.4    De Logu, A.5
  • 15
    • 80052040788 scopus 로고    scopus 로고
    • Synthesis biological activity of some novel hydrazones containing triazole thiazole
    • (e) K. Ablajan, Synthesis biological activity of some novel hydrazones containing triazole thiazole, Chin. J. Org. Chem. 31 (2011) 724-727;
    • (2011) Chin. J. Org. Chem. , vol.31 , pp. 724-727
    • Ablajan, K.1
  • 16
    • 79961143190 scopus 로고    scopus 로고
    • An efficient synthesis of N- (1-arylethylidene)-N′-(4-arylthiazol- 2-yl)hydrazones from α,α-dibromoacetophenones and N-(1-arylethylidene) thiosemicarbazones
    • (f) R. Pundeer, V.K. Sushma, O. Prakash, S.C. Bhatia, An efficient synthesis of N- (1-arylethylidene)-N′-(4-arylthiazol-2-yl)hydrazones from α,α-dibromoacetophenones and N-(1-arylethylidene) thiosemicarbazones, Pharm. Chem. 3 (2011) 109-114.
    • (2011) Pharm. Chem. , vol.3 , pp. 109-114
    • Pundeer, R.1    Sushma, V.K.2    Prakash, O.3    Bhatia, S.C.4
  • 17
    • 79961091795 scopus 로고    scopus 로고
    • Highly efficient synthesis of β-amino Ketones via direct Mannich-type reaction catalyzed by acidic ionic liquid
    • (a) D.N. Zhang, J.T. Li, Y.L. Song, G.F. Chen, Highly efficient synthesis of β-amino Ketones via direct Mannich-type reaction catalyzed by acidic ionic liquid, Lett. Org. Chem. 8 (2011) 385-390;
    • (2011) Lett. Org. Chem. , vol.8 , pp. 385-390
    • Zhang, D.N.1    Li, J.T.2    Song, Y.L.3    Chen, G.F.4
  • 18
    • 79952021005 scopus 로고    scopus 로고
    • Multicomponent one-pot synthesis of substituted Hantzsch thiazole derivatives under solvent free conditions
    • (b) B. Dawane, S. Konda, V. Kamble, S. Chavan, A.B. Bhosale, S. Baseerm, Multicomponent one-pot synthesis of substituted Hantzsch thiazole derivatives under solvent free conditions, Eur. J. Chem. 6 (2009) S358-S362.
    • (2009) Eur. J. Chem. , vol.6
    • Dawane, B.1    Konda, S.2    Kamble, V.3    Chavan, S.4    Bhosale, A.B.5    Baseerm, S.6
  • 19
    • 34247637304 scopus 로고    scopus 로고
    • An efficient and green procedure for the preparation of 2-{2-[N-(2-hydroxybenzylidene)hydrazino]thiazol-4-yl}phenols
    • DOI 10.1071/CH06377
    • V.T. Kamble, B.S. Davane, S.A. Chavan, R.B. Bhosale, An efficient and green procedure for the preparation of 2-{2-[N-(2-hydroxybenzylidene)hydrazino]- thiazol-4-yl}phenols, Aust. J. Chem. 60 (2007) 302-304. (Pubitemid 46674927)
    • (2007) Australian Journal of Chemistry , vol.60 , Issue.4 , pp. 302-304
    • Kamble, V.T.1    Davane, B.S.2    Chavan, S.A.3    Bhosale, R.B.4
  • 20
    • 42749088162 scopus 로고    scopus 로고
    • Catalyst-free efficient synthesis of 2-aminothiazoles in water at ambient temperature
    • (a) T.M. Potewar, S.A. Ingale, K.V. Srinivasan, Catalyst-free efficient synthesis of 2-aminothiazoles in water at ambient temperature, Tetrahedron 64 (2008) 5019-5022;
    • (2008) Tetrahedron , vol.64 , pp. 5019-5022
    • Potewar, T.M.1    Ingale, S.A.2    Srinivasan, K.V.3
  • 24
    • 33646107336 scopus 로고    scopus 로고
    • Some applications of ultrasound irradiation in organic synthesis
    • (c) J.T. Li, S.X. Wang, G.F. Chen, T.S. Li, Some applications of ultrasound irradiation in organic synthesis, Curr. Org. Synth. 2 (2005) 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.