메뉴 건너뛰기




Volumn 19, Issue 2, 2012, Pages 307-313

Ultrasound-promoted catalyst-free one-pot four component synthesis of 2H-indazolo[2,1-b]phthalazine-triones in neutral ionic liquid 1-butyl-3-methylimidazolium bromide

Author keywords

1 Butyl 3 methylimidazolium bromide; 2H Indazolo 2,1 b phthalazine trione; Catalyst free reaction; Combinatorial chemistry; Multi component reaction; Ultrasound

Indexed keywords

ALDEHYDES; BIOCHIPS; CATALYSTS; ULTRASONICS;

EID: 84860407032     PISSN: 13504177     EISSN: 18732828     Source Type: Journal    
DOI: 10.1016/j.ultsonch.2011.07.011     Document Type: Article
Times cited : (100)

References (72)
  • 2
    • 37049080018 scopus 로고
    • Sonochemistry. Part 1. The physical aspects
    • T.J. Mason, and J.P. Lorimer Sonochemistry. Part 1. The physical aspects Chem. Soc. Rev. 16 1987 239 274
    • (1987) Chem. Soc. Rev. , vol.16 , pp. 239-274
    • Mason, T.J.1    Lorimer, J.P.2
  • 3
    • 33646107336 scopus 로고    scopus 로고
    • Some applications of ultrasound irradiation in organic synthesis
    • J.T. Li, S.X. Wang, G.F. Chen, and 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
  • 4
    • 33645222276 scopus 로고    scopus 로고
    • Power ultrasound in organic synthesis: Moving cavitational chemistry from academia to innovative and large-scale applications
    • DOI 10.1039/b503848k
    • G. Cravotto, and P. Cintas Power ultrasound in organic synthesis: moving cavitational chemistry from academia to innovative and large-scale applications Chem. Soc. Rev. 35 2006 180 196 (Pubitemid 43485008)
    • (2006) Chemical Society Reviews , vol.35 , Issue.2 , pp. 180-196
    • Cravotto, G.1    Cintas, P.2
  • 6
    • 60749129757 scopus 로고    scopus 로고
    • Ultrasound in heterocycles chemistry
    • R. Cella, and H. Stefani Ultrasound in heterocycles chemistry Tetrahedron 65 2009 2619 2641
    • (2009) Tetrahedron , vol.65 , pp. 2619-2641
    • Cella, R.1    Stefani, H.2
  • 9
    • 33144479521 scopus 로고    scopus 로고
    • Ultrasound-assisted synthesis of 1,8-dioxoocta hydroxanthene derivatives catalyzed by p-dodecylbenzenesulfonic acid in aqueous media
    • T.S. Jin, J.S. Zhang, A.Q. Wang, and T.S. Li Ultrasound-assisted synthesis of 1,8-dioxoocta hydroxanthene derivatives catalyzed by p-dodecylbenzenesulfonic acid in aqueous media Ultrason. Sonochem. 13 2006 220 224
    • (2006) Ultrason. Sonochem. , vol.13 , pp. 220-224
    • Jin, T.S.1    Zhang, J.S.2    Wang, A.Q.3    Li, T.S.4
  • 10
    • 33749534257 scopus 로고    scopus 로고
    • Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings
    • DOI 10.1016/j.tetlet.2006.09.043, PII S0040403906018296
    • K.P. Guzen, R. Cella, and H.A. Stefani Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings Tetrahedron Lett. 47 2006 8133 8136 (Pubitemid 44528660)
    • (2006) Tetrahedron Letters , vol.47 , Issue.46 , pp. 8133-8136
    • Guzen, K.P.1    Cella, R.2    Stefani, H.A.3
  • 11
    • 35848929258 scopus 로고    scopus 로고
    • An efficient synthesis of pyrido[2,3-d]pyrimidine derivatives and related compounds under ultrasound irradiation without catalyst
    • DOI 10.1016/j.ultsonch.2007.03.002, PII S1350417707000582
    • S. Tu, L. Cao, Y. Zhang, Q. Shao, D. Zhou, and C. Li An efficient synthesis of pyrido[2,3-d]pyrimidine derivatives and related compounds under ultrasound irradiation without catalyst Ultrason. Sonochem. 15 2008 217 221 (Pubitemid 350061180)
    • (2008) Ultrasonics Sonochemistry , vol.15 , Issue.3 , pp. 217-221
    • Tu, S.1    Cao, L.2    Zhang, Y.3    Shao, Q.4    Zhou, D.5    Li, C.6
  • 13
    • 51449094400 scopus 로고    scopus 로고
    • Ultrasound assisted synthesis of some new 1,3,4-thiadiazole and bi(1,3,4-thiadiazole) derivatives incorporating pyrazolone moiety
    • N.M.A. El-Rahman, T.S. Saleh, and M.F. Mady Ultrasound assisted synthesis of some new 1,3,4-thiadiazole and bi(1,3,4-thiadiazole) derivatives incorporating pyrazolone moiety Ultrason. Sonochem. 16 2009 70 74
    • (2009) Ultrason. Sonochem. , vol.16 , pp. 70-74
    • El-Rahman, N.M.A.1    Saleh, T.S.2    Mady, M.F.3
  • 14
    • 74349112543 scopus 로고    scopus 로고
    • An efficient ultrasound promoted method for the one-pot synthesis of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivatives
    • H. Zang, Y. Zhang, Y. Zhang, and B.W. Cheng An efficient ultrasound promoted method for the one-pot synthesis of 7,10,11,12-tetrahydrobenzo[c] acridin-8(9H)-one derivatives Ultrason. Sonochem. 17 2010 495 499
    • (2010) Ultrason. Sonochem. , vol.17 , pp. 495-499
    • Zang, H.1    Zhang, Y.2    Zhang, Y.3    Cheng, B.W.4
  • 15
    • 77956433940 scopus 로고    scopus 로고
    • Ultrasound promoted greener synthesis of 2-(3,5-diaryl-4,5-dihydro-1H- pyrazol-1-yl)-4-phenylthiazoles
    • D. Venzke, A.F.C. Flores, F.H. Quina, L. Pizzuti, and C.M.P. Pereira Ultrasound promoted greener synthesis of 2-(3,5-diaryl-4,5-dihydro-1H-pyrazol-1- yl)-4-phenylthiazoles Ultrason. Sonochem 18 2011 370 374
    • (2011) Ultrason. Sonochem , vol.18 , pp. 370-374
    • Venzke, D.1    Flores, A.F.C.2    Quina, F.H.3    Pizzuti, L.4    Pereira, C.M.P.5
  • 16
    • 0034665244 scopus 로고    scopus 로고
    • Maximizing synthetic efficiency: Multi-component transformations lead the way
    • H. Bienayme, C. Hulme, G. Oddon, and P. Schmitt Maximizing synthetic efficiency: multi-component transformations lead the way Chem. Eur. J. 6 2000 3321 3329
    • (2000) Chem. Eur. J. , vol.6 , pp. 3321-3329
    • Bienayme, H.1    Hulme, C.2    Oddon, G.3    Schmitt, P.4
  • 17
    • 1642271331 scopus 로고    scopus 로고
    • Paradigm confirmed: The first use of ionic liquids to dramatically influence the outcome of chemical reactions
    • DOI 10.1021/ol036310e
    • M.J. Earle, S.P. Katdare, and K.R. Seddon Paradigm confirmed: the first use of ionic liquids to dramatically influence the outcome of chemical reactions Org. Lett. 6 2004 707 710 (Pubitemid 38387956)
    • (2004) Organic Letters , vol.6 , Issue.5 , pp. 707-710
    • Earle, M.J.1    Katdare, S.P.2    Seddon, K.R.3
  • 18
    • 0033432259 scopus 로고    scopus 로고
    • Diels-Alder reactions in ionic liquids. A safe recyclable alternative to lithium perchlorate-diethyl ether mixtures
    • M.J. Earle, P.B. McCormac, and K.R. Seddon Diels-Alder reactions in ionic liquids. A safe recyclable alternative to lithium perchlorate-diethyl ether mixtures Green Chem. 1 1999 23 25
    • (1999) Green Chem. , vol.1 , pp. 23-25
    • Earle, M.J.1    McCormac, P.B.2    Seddon, K.R.3
  • 19
    • 1542286578 scopus 로고    scopus 로고
    • Charge transfer polymerization in ionic liquids
    • R. Vijayaraghavan, and D.R. MacFarlane Charge transfer polymerization in ionic liquids Aust. J. Chem. 57 2004 129 133
    • (2004) Aust. J. Chem. , vol.57 , pp. 129-133
    • Vijayaraghavan, R.1    MacFarlane, D.R.2
  • 20
    • 0035821357 scopus 로고    scopus 로고
    • Ionic liquids as a recyclable reaction medium for the Baylis-Hillman reaction
    • DOI 10.1016/S0040-4020(01)00316-7, PII S0040402001003167
    • J.N. Rosa, C.A.M. Afonso, and A.G. Santos Ionic liquids as a recyclable reaction medium for the Baylis-Hillman reaction Tetrahedron 57 2001 4189 4193 (Pubitemid 32406237)
    • (2001) Tetrahedron , vol.57 , Issue.19 , pp. 4189-4193
    • Rosa, J.N.1    Afonso, C.A.M.2    Santos, A.G.3
  • 21
    • 33748251571 scopus 로고    scopus 로고
    • A novel class of versatile solvents for two-phase catalysis: Hydrogenation, isomerization, and hydroformylation of alkenes catalyzed by rhodium complexes in liquid 1,3-dialkylimidazolium salts
    • Y. Chauvin, L. Mussmann, and H. Olivier A novel class of versatile solvents for two-phase catalysis: Hydrogenation, isomerization, and hydroformylation of alkenes catalyzed by rhodium complexes in liquid 1,3-aialkylimidazolium salts Angew. Chem., Int. Ed. Engl. 34 1995 2698 2700 (Pubitemid 126675758)
    • (1996) Angewandte Chemie (International Edition in English) , vol.34 , Issue.23-24 , pp. 2698-2700
    • Chauvin, Y.1    Mussmann, L.2    Olivier, H.3
  • 22
    • 22944433453 scopus 로고    scopus 로고
    • Palladium-catalyzed hydroesterification of styrene derivatives in the presence of ionic liquids
    • DOI 10.1016/j.jorganchem.2005.05.031, PII S0022328X05004171, Ionic Liquids
    • M.A. Klingshirn, R.D. Rogers, and K.H. Shaughnessy Palladium-catalyzed hydroesterification of styrene derivatives in the presence of ionic liquids J. Organomet. Chem. 690 2005 3620 3626 (Pubitemid 41042489)
    • (2005) Journal of Organometallic Chemistry , vol.690 , Issue.15 , pp. 3620-3626
    • Klingshirn, M.A.1    Rogers, R.D.2    Shaughnessy, K.H.3
  • 23
    • 57249111527 scopus 로고    scopus 로고
    • Palladium-catalysed carbonylation of aryl halides in ionic liquid media: high catalyst stability and significant rate-enhancement in alkoxycarbonylation
    • DOI 10.1039/b100951f
    • E. Mizushima, T. Hayashi, and M. Tanaka Palladium-catalysed carbonylation of aryl halides in ionic liquid media: high catalyst stability and significant rate-enhancement in alkoxycarbonylation Green Chem. 3 2001 76 79 (Pubitemid 33264166)
    • (2001) Green Chemistry , vol.3 , Issue.2 , pp. 76-79
    • Mizushima, E.1    Hayashi, T.2    Tanaka, M.3
  • 24
    • 27744578648 scopus 로고    scopus 로고
    • 2 immobilized in ionic liquids
    • DOI 10.1016/j.tet.2005.07.095
    • J.S. Yadav, B.V.S. Reddy, G. Baishya, K.V. Reddy, and A.V. Narsaiah Conjugate addition of indoles to α,β-unsaturated ketones using Cu(OTf)2 immobilized in ionic liquids Tetrahedron 61 2005 9541 9544 (Pubitemid 41583473)
    • (2005) Tetrahedron , vol.61 , Issue.40 , pp. 9541-9544
    • Yadav, J.S.1    Reddy, B.V.S.2    Baishya, G.3    Reddy, K.V.4    Narsaiah, A.V.5
  • 27
    • 0242466540 scopus 로고    scopus 로고
    • Selective palladium-catalysed dimerisation of methyl acrylate in ionic liquids: Towards a continuous process
    • DOI 10.1039/b212028n
    • (M. Picquet, S. Stutzmann, I. Tkatchenko, I. Tommasi, J. Zimmermann, and P. Wasserscheid Selective palladium-catalysed dimerisation of methyl acrylate in ionic liquids: towards a continuous process Green Chem. 5 2003 153 162 (Pubitemid 37487471)
    • (2003) Green Chemistry , vol.5 , Issue.2 , pp. 153-162
    • Picquet, M.1    Stutzmann, S.2    Tkatchenko, I.3    Tommasi, I.4    Zimmermann, J.5    Wasserscheid, P.6
  • 28
    • 14844333561 scopus 로고    scopus 로고
    • Utilisation of ionic liquid solvents for the synthesis of Lily-of-the-Valley fragrance {β-Lilial®; 3-(4-t-butylphenyl)-2- methylpropanal}
    • DOI 10.1016/j.molcata.2004.12.022, PII S1381116904009318
    • S.A. Forsyth, H.Q.N. Gunaratne, C. Hardacre, A. McKeown, D.W. Rooney, and K.R. Seddon Utilisation of ionic liquid solvents for the synthesis of Lily-of-the-Valley fragrance {β-Lilial; 3-(4-t-butylphenyl)-2- methylpropanal} J. Mol. Catal. A: Chem. 231 2005 61 66 (Pubitemid 40348720)
    • (2005) Journal of Molecular Catalysis A: Chemical , vol.231 , Issue.1-2 , pp. 61-66
    • Forsyth, S.A.1    Gunaratne, H.Q.N.2    Hardacre, C.3    McKeown, A.4    Rooney, D.W.5    Seddon, K.R.6
  • 29
    • 0037035632 scopus 로고    scopus 로고
    • Biocatalysis in ionic liquids: Batchwise and continuous flow processes using supercritical carbon dioxide as the mobile phase
    • M.T. Reetz, W. Wiesenhoefer, G. Francio, and W. Leitner Biocatalysis in ionic liquids: batchwise and continuous flow processes using supercritical carbon dioxide as the mobile phase Chem. Commun. 2002 992 993 (Pubitemid 34494115)
    • (2002) Chemical Communications , Issue.9 , pp. 992-993
    • Reetz, M.T.1    Wiesenhofer, W.2    Francio, G.3    Leitner, W.4
  • 31
    • 42749088162 scopus 로고    scopus 로고
    • Catalyst-free efficient synthesis of 2-aminothiazoles in water at ambient temperature
    • T.M. Potewar, S.A. Ingale, and 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
  • 32
    • 45849146122 scopus 로고    scopus 로고
    • A catalyst-free N-benzyloxycarbonylation of amines in aqueous micellar media at room temperature
    • J.J. Shrikhande, M.B. Gawande, and R.V. Jayaram A catalyst-free N-benzyloxycarbonylation of amines in aqueous micellar media at room temperature Tetrahedron Lett. 49 2008 4799 4803
    • (2008) Tetrahedron Lett. , vol.49 , pp. 4799-4803
    • Shrikhande, J.J.1    Gawande, M.B.2    Jayaram, R.V.3
  • 33
    • 46449087203 scopus 로고    scopus 로고
    • Solvent-free synthesis of benzoic esters and benzyl esters in novel Brønsted acidic ionic liquids under microwave irradiation
    • X. Li, W. Eli, and G. Li Solvent-free synthesis of benzoic esters and benzyl esters in novel Brønsted acidic ionic liquids under microwave irradiation Catal. Commun. 9 2008 2264 2268
    • (2008) Catal. Commun. , vol.9 , pp. 2264-2268
    • Li, X.1    Eli, W.2    Li, G.3
  • 34
    • 49149110564 scopus 로고    scopus 로고
    • Solvent- and catalyst-free gem-bisallylation of carboxylic acid derivatives with allylzinc bromide
    • Y. Wei, H. Ren, and J. Wang Solvent- and catalyst-free gem-bisallylation of carboxylic acid derivatives with allylzinc bromide Tetrahedron Lett. 49 2008 5697 5699
    • (2008) Tetrahedron Lett. , vol.49 , pp. 5697-5699
    • Wei, Y.1    Ren, H.2    Wang, J.3
  • 35
    • 40949091578 scopus 로고    scopus 로고
    • Catalyst-free synthesis of polyorganosiloxanes by high temperature & pressure water
    • T. Ogawa, J. Watanabe, and Y. Oshima Catalyst-free synthesis of polyorganosiloxanes by high temperature & pressure water Supercrit. Fluids 45 45 2008 80 87
    • (2008) Supercrit. Fluids , vol.45 , Issue.45 , pp. 80-87
    • Ogawa, T.1    Watanabe, J.2    Oshima, Y.3
  • 36
    • 78149304818 scopus 로고    scopus 로고
    • Catalyst-free one-pot four component synthesis of polysubstituted imidazoles in neutral ionic liquid 1-butyl-3-methylimidazolium bromide
    • A. Hasaninejad, A. Zare, M. Shekouhy, and J. Ameri-Rad Catalyst-free one-pot four component synthesis of polysubstituted imidazoles in neutral ionic liquid 1-butyl-3-methylimidazolium bromide J. Comb. Chem. 12 2010 844 849
    • (2010) J. Comb. Chem. , vol.12 , pp. 844-849
    • Hasaninejad, A.1    Zare, A.2    Shekouhy, M.3    Ameri-Rad, J.4
  • 37
    • 0036736760 scopus 로고    scopus 로고
    • Unsaturated O- and N-Heterocycles from carbohydrate feedstocks
    • F.W. Lichtenthaler Unsaturated O- and N-Heterocycles from carbohydrate feedstocks Acc. Chem. Res. 35 2002 728 737
    • (2002) Acc. Chem. Res. , vol.35 , pp. 728-737
    • Lichtenthaler, F.W.1
  • 38
    • 33744916975 scopus 로고    scopus 로고
    • Multicomponent cascade heterocyclisation as a promising route to targeted synthesis of polyfunctional pyridines
    • DOI 10.1070/RC2003v072n01ABEH000764
    • V.P. Litvinov Multi-component cascade heterocyclisation as a promising route to targeted synthesis of polyfunctional pyridines Russ. Chem. Rev. 72 72 2003 69 85 (Pubitemid 44352214)
    • (2003) Russian Chemical Reviews , vol.72 , Issue.1 , pp. 69-85
    • Litvinov, V.P.1
  • 39
    • 78650518437 scopus 로고    scopus 로고
    • A rapid, one-pot, four-component route to 2H-indazolo[2,1-b]phthalazine- triones
    • E. Mosaddegh, and A. Hassankhani A rapid, one-pot, four-component route to 2H-indazolo[2,1-b]phthalazine-triones Tetrahedron Lett. 52 2011 488 490
    • (2011) Tetrahedron Lett. , vol.52 , pp. 488-490
    • Mosaddegh, E.1    Hassankhani, A.2
  • 40
    • 0345976562 scopus 로고
    • Bridgehead hydrazines. 3. Unusual photorearrangement of 1,4-diphenylpyridazino[1,2-b]phthalazine-6,11-dione
    • T. Sheradsky, and R. Moshenberg Bridgehead hydrazines. 3. Unusual photorearrangement of 1,4-diphenylpyridazino[1,2-b]phthalazine-6,11-dione J. Org. Chem. 51 1986 3123 3125
    • (1986) J. Org. Chem. , vol.51 , pp. 3123-3125
    • Sheradsky, T.1    Moshenberg, R.2
  • 41
    • 0037123412 scopus 로고    scopus 로고
    • Synthesis and evaluation of keto-glutamine analogues as inhibitors of hepatitis A virus 3C proteinase
    • DOI 10.1021/jo0157831
    • Y.K. Ramtohup, M.N.G. James, and J.C. Vederas Synthesis and evaluation of keto-glutamine analogues as inhibitors of hepatitis A virus 3C proteinase J. Org. Chem. 67 2002 3169 3178 (Pubitemid 34517693)
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.10 , pp. 3169-3178
    • Ramtohul, Y.K.1    James, M.N.G.2    Vederas, J.C.3
  • 42
    • 33646761329 scopus 로고
    • Highly regioselective ring opening of epoxides and aziridines using (bromodimethyl)sulfonium bromide
    • A. Csampai, K. Kormendy, and F. Ruff Highly regioselective ring opening of epoxides and aziridines using (bromodimethyl)sulfonium bromide Tetrahedron 47 1991 4457 4460
    • (1991) Tetrahedron , vol.47 , pp. 4457-4460
    • Csampai, A.1    Kormendy, K.2    Ruff, F.3
  • 43
    • 34147125865 scopus 로고    scopus 로고
    • 2-Mediated novel 1,3-dipolar cycloaddition of methylenecyclopropanes (MCPs) vinylidenecyclopropanes (VCPs) and methylenecyclobutane (MCB) with phthalhydrazide
    • 2-Mediated novel 1,3-dipolar cycloaddition of methylenecyclopropanes (MCPs) vinylidenecyclopropanes (VCPs) and methylenecyclobutane (MCB) with phthalhydrazide Org. Lett. 9 2007 1303 1306
    • (2007) Org. Lett. , vol.9 , pp. 1303-1306
    • Liu, L.P.1    Lu, J.M.2    Shi, M.3
  • 44
    • 38649136593 scopus 로고    scopus 로고
    • One-pot, three-component route to 2H-indazolo[2,1-b]phthalazine-triones
    • M. Sayyafi, M. Seyyedhamzeh, H.R. Khavasi, and A. Bazgir One-pot, three-component route to 2H-indazolo[2,1-b]phthalazine-triones Tetrahedron 64 2008 2375 2378
    • (2008) Tetrahedron , vol.64 , pp. 2375-2378
    • Sayyafi, M.1    Seyyedhamzeh, M.2    Khavasi, H.R.3    Bazgir, A.4
  • 46
    • 80052716275 scopus 로고    scopus 로고
    • Heteropoly Acid in ionic liquid - An efficient catalyst for the preparation of 2H-Indazolo[2,1-b]phthalazine-triones
    • R. Fazaeli, H. Aliyan, and N. Fazaeli Heteropoly Acid in ionic liquid - an efficient catalyst for the preparation of 2H-Indazolo[2,1-b]phthalazine- triones The Open Cat. J. 3 2010 14 16
    • (2010) The Open Cat. J. , vol.3 , pp. 14-16
    • Fazaeli, R.1    Aliyan, H.2    Fazaeli, N.3
  • 47
    • 84860394581 scopus 로고    scopus 로고
    • Starch sulfate as an efficient and biodegradable polymer catalyst for one-pot, four-component reaction of 2H-indazolo[2,1-b]phthalazine-triones
    • H. Shaterian, and F. Rigi Starch sulfate as an efficient and biodegradable polymer catalyst for one-pot, four-component reaction of 2H-indazolo[2,1-b]phthalazine-triones Starch 00 2011 1 7
    • (2011) Starch , vol.0 , pp. 1-7
    • Shaterian, H.1    Rigi, F.2
  • 48
    • 78650518437 scopus 로고    scopus 로고
    • A rapid, one-pot, four-component route to 2H-indazolo[2,1-b]-phthalazine- triones
    • E. Mosaddegh, and A. Hassankhani A rapid, one-pot, four-component route to 2H-indazolo[2,1-b]-phthalazine-triones Tetrahedron Lett. 52 2011 488 490
    • (2011) Tetrahedron Lett. , vol.52 , pp. 488-490
    • Mosaddegh, E.1    Hassankhani, A.2
  • 49
    • 62549102472 scopus 로고    scopus 로고
    • Reusable silica supported poly phosphoric acid catalyzed three-component synthesis of 2H-indazolo[2,1-b]phthalazine-trione derivatives
    • H. Shaterian, A. Hosseinian, and M. Ghashang Reusable silica supported poly phosphoric acid catalyzed three-component synthesis of 2H-indazolo[2,1-b] phthalazine-trione derivatives Arkivoc ii 2009 59 67
    • (2009) Arkivoc , vol.II , pp. 59-67
    • Shaterian, H.1    Hosseinian, A.2    Ghashang, M.3
  • 52
    • 79951807063 scopus 로고    scopus 로고
    • Efficient synthesis of 4,4α-(arylmethylene)-bis(3-methyl-1- phenylpyrazol-5-ol) derivatives in PEG-400 under catalyst-free conditions
    • A. Hasaninejad, A. Zare, M. Shekouhy, and N. Golzar Efficient synthesis of 4,4α-(arylmethylene)-bis(3-methyl-1-phenylpyrazol-5-ol) derivatives in PEG-400 under catalyst-free conditions Org. Prep. Proc. Int. 43 2011 131 137
    • (2011) Org. Prep. Proc. Int. , vol.43 , pp. 131-137
    • Hasaninejad, A.1    Zare, A.2    Shekouhy, M.3    Golzar, N.4
  • 53
    • 67650287693 scopus 로고    scopus 로고
    • A catalyst-free protocol for the green and efficient condensation of indoles with aldehydes in ionic liquids
    • A. Zare, A. Parhami, A.R. Moosavi-Zare, A. Hasaninejad, A. Khalafi-Nezhad, and M.H. Beyzavi A catalyst-free protocol for the green and efficient condensation of indoles with aldehydes in ionic liquids Can. J. Chem. 87 2009 416 421
    • (2009) Can. J. Chem. , vol.87 , pp. 416-421
    • Zare, A.1    Parhami, A.2    Moosavi-Zare, A.R.3    Hasaninejad, A.4    Khalafi-Nezhad, A.5    Beyzavi, M.H.6
  • 54
    • 33846490499 scopus 로고    scopus 로고
    • Preparation of 1-butyl-3-methyl imidazolium-based room temperature ionic liquids
    • J. Dupont, C.S. Consorti, P.A.Z. Suarez, and R.F. de Souza Preparation of 1-butyl-3-methyl imidazolium-based room temperature ionic liquids Org. Synth. Coll. 10 2004 184 187
    • (2004) Org. Synth. Coll. , vol.10 , pp. 184-187
    • Dupont, J.1    Consorti, C.S.2    Suarez, P.A.Z.3    De Souza, R.F.4
  • 55
    • 0037184423 scopus 로고    scopus 로고
    • Characterizing ionic liquids on the basis of multiple solvation interactions
    • DOI 10.1021/ja028156h
    • J.L. Anderson, J. Ding, T. Welton, and D.W. Armstrong Characterizing ionic liquids on the basis of multiple solvation interactions J. Am. Chem. Soc. 124 2002 14247 14254 (Pubitemid 35386876)
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.47 , pp. 14247-14254
    • Anderson, J.L.1    Ding, J.2    Welton, T.3    Armstrong, D.W.4
  • 56
    • 13144257725 scopus 로고    scopus 로고
    • Room-temperature ionic liquids that dissolve carbohydrates in high concentrations
    • DOI 10.1039/b412848f
    • Q. Liu, M.H.A. Jonssen, F. Rantwijk, and R.A. Sheldon Room-temperature ionic liquids that dissolve carbohydrates in high concentrations Green Chem. 7 2005 39 42 (Pubitemid 40179326)
    • (2005) Green Chemistry , vol.7 , Issue.1 , pp. 39-42
    • Liu, Q.1    Janssen, M.H.A.2    Van Rantwijk, F.3    Sheldon, R.A.4
  • 58
    • 31444448205 scopus 로고    scopus 로고
    • An efficient and clean synthesis of bis(indolyl)methanes in a protic solvent at room temperature
    • DOI 10.1016/j.tetlet.2005.12.093, PII S0040403905027929
    • M.L. Deb, and P.J. Bhuyan An efficient and clean synthesis of bis(indolyl)methanes in a protic solvent at room temperature Tetrahedron Lett. 47 2006 1441 1443 (Pubitemid 43151159)
    • (2006) Tetrahedron Letters , vol.47 , Issue.9 , pp. 1441-1443
    • Deb, M.L.1    Bhuyan, P.J.2
  • 59
    • 0037267253 scopus 로고    scopus 로고
    • Sonochemical reactors for waste water treatment: Comparison using formic acid degradation as a model reaction
    • DOI 10.1016/S1093-0191(01)00133-2, PII S1093019101001332
    • P.R. Gogate, S. Mujumdar, and A.B. Pandit Sonochemical reactors for waste water treatment: comparison using formic acid degradation as a model reaction Adv. Environ. Res. 7 2003 283 299 (Pubitemid 36196775)
    • (2003) Advances in Environmental Research , vol.7 , Issue.2 , pp. 283-299
    • Gogate, P.R.1    Mujumdar, S.2    Pandit, A.B.3
  • 60
    • 0038009156 scopus 로고    scopus 로고
    • Sonochemistry and sonoprocessing: The link, the trends and (probably) the future
    • DOI 10.1016/S1350-4177(03)00086-5
    • T.J. Mason Sonochemistry sonoprocessing: the link the trends and (pobably) the future Ultrason. Sonochem. 10 2003 175 179 (Pubitemid 36724667)
    • (2003) Ultrasonics Sonochemistry , vol.10 , Issue.4-5 , pp. 175-179
    • Mason, T.J.1
  • 62
    • 35349001335 scopus 로고    scopus 로고
    • Sono-synthesis of imidazolidine-2-thione as a base compound of some pharmaceutical products
    • DOI 10.1016/j.ultsonch.2007.02.006, PII S1350417707000478
    • M.H. Entezari, A. Asghari, and F. Hadizadeh Sono-synthesis of imidazolidine-2-thione as a base compound of some pharmaceutical products Ultrason. Sonochem. 15 2008 119 123 (Pubitemid 47600656)
    • (2008) Ultrasonics Sonochemistry , vol.15 , Issue.2 , pp. 119-123
    • Entezari, M.H.1    Asghari, A.2    Hadizadeh, F.3
  • 63
    • 29544452809 scopus 로고    scopus 로고
    • Ultrasound-accelerated synthesis of 1,4-dihydropyridines in an ionic liquid
    • DOI 10.1007/s00706-005-0405-9
    • A. Shaabani, A.H. Rezayan, A. Rahmati, and M. Sharifi Ultrasound-accelerated synthesis of 1,4-dihydropyridines in an ionic liquid Monatsh Chem. 137 2006 77 81 (Pubitemid 43016873)
    • (2006) Monatshefte fur Chemie , vol.137 , Issue.1 , pp. 77-81
    • Shaabani, A.1    Rezayan, A.H.2    Rahmati, A.3    Sharifi, M.4
  • 64
    • 0031326125 scopus 로고    scopus 로고
    • Ultrasound in synthetic organic chemistry
    • T.J. Manson Ultrasound in synthetic organic chemistry Chem. Soc. Rev. 26 1997 443 451
    • (1997) Chem. Soc. Rev. , vol.26 , pp. 443-451
    • Manson, T.J.1
  • 65
    • 0007066464 scopus 로고    scopus 로고
    • Green chemistry. The sonochemical approach
    • P. Cintas, and J.L. Luche Green chemistry. The sonochemical approach Green Chem. 1 1999 115 125
    • (1999) Green Chem. , vol.1 , pp. 115-125
    • Cintas, P.1    Luche, J.L.2
  • 66
    • 0035121161 scopus 로고    scopus 로고
    • Salt effects on Diels-Alder reaction kinetics
    • A. Kumar Salt effects on Diels-Alder reaction kinetics Chem. Rev. 101 2001 1 20
    • (2001) Chem. Rev. , vol.101 , pp. 1-20
    • Kumar, A.1
  • 67
    • 0347417134 scopus 로고    scopus 로고
    • Room-temperature ionic liquids. Solvents for synthesis and catalysis
    • T. Welton Room-temperature ionic liquids. Solvents for synthesis and catalysis Chem. Rev. 99 1999 2071 2084
    • (1999) Chem. Rev. , vol.99 , pp. 2071-2084
    • Welton, T.1
  • 68
    • 0000034575 scopus 로고    scopus 로고
    • Ionic liquids - New ''solutions" for transition metal catalysis
    • P. Wasserscheid, and W. Keim Ionic liquids - new ''solutions" for transition metal catalysis Angew. Chem. Int. Ed. 39 2000 3772 3789
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3772-3789
    • Wasserscheid, P.1    Keim, W.2
  • 69
    • 0035824303 scopus 로고    scopus 로고
    • Catalytic reactions in ionic liquids
    • R. Sheldon Catalytic reactions in ionic liquids Chem. Commun. 2001 2399 2407 (Pubitemid 33124059)
    • (2001) Chemical Communications , Issue.23 , pp. 2399-2407
    • Sheldon, R.1
  • 70
    • 0036776442 scopus 로고    scopus 로고
    • Improved synthesis of chalcones under ultrasound irradiation
    • J.T. Li, W.Z. Yang, S.X. Wang, S.H. Li, and T.S. Li Improved synthesis of chalcones under ultrasound irradiation Ultrason. Sonochem. 9 2002 237 239
    • (2002) Ultrason. Sonochem. , vol.9 , pp. 237-239
    • Li, J.T.1    Yang, W.Z.2    Wang, S.X.3    Li, S.H.4    Li, T.S.5
  • 72
    • 34848918805 scopus 로고    scopus 로고
    • Synthesis of N-alkoxyphthalimides under ultrasound irradiation
    • S.X. Wang, X.W. Li, and J.T. Li Synthesis of N-alkoxyphthalimides under ultrasound irradiation Ultrason. Sonochem. 15 2008 33 36
    • (2008) Ultrason. Sonochem. , vol.15 , pp. 33-36
    • Wang, S.X.1    Li, X.W.2    Li, J.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.