메뉴 건너뛰기




Volumn , Issue , 2013, Pages

Nio nanoparticles: An efficient catalyst for the multicomponent one-pot synthesis of novel spiro and condensed indole derivatives

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84867005781     PISSN: 20909063     EISSN: 20909071     Source Type: Journal    
DOI: 10.1155/2013/606259     Document Type: Article
Times cited : (33)

References (63)
  • 1
    • 0041586059 scopus 로고
    • Heterogeneous catalytic oxidations in the manufacture of fine chemicals
    • 10.1016/0920-5861(94)80186-X
    • Sheldon R. A., Dakka J., Heterogeneous catalytic oxidations in the manufacture of fine chemicals. Catalysis Today 1994 19 2 215 245 10.1016/0920-5861(94)80186-X
    • (1994) Catalysis Today , vol.19 , Issue.2 , pp. 215-245
    • Sheldon, R.A.1    Dakka, J.2
  • 2
    • 0347933770 scopus 로고    scopus 로고
    • Catalysis and pollution prevention
    • Sheldon R. A., Catalysis and pollution prevention. Chemistry & Industry 1997 1 12 15
    • (1997) Chemistry & Industry , vol.1 , pp. 12-15
    • Sheldon, R.A.1
  • 3
    • 21844444274 scopus 로고    scopus 로고
    • Catalysis of liquid phase organic reactions using chemically modified mesoporous inorganic solids
    • Clark J. H., Mac Quarrie D. J., Catalysis of liquid phase organic reactions using chemically modified mesoporous inorganic solids. Chemical Communications 1998 8 853 860 10.1039/a709143e (Pubitemid 128675425)
    • (1998) Chemical Communications , Issue.8 , pp. 853-860
    • Clark, J.H.1    Macquarrie, D.J.2
  • 4
    • 0033530917 scopus 로고    scopus 로고
    • Heterogeneous catalytic transformations for environmentally friendly production
    • PII S0926860X99002744
    • Sheldon R. A., Downing R. S., Heterogeneous catalytic transformations for environmentally friendly production. Applied Catalysis A 1999 189 2 163 183 10.1016/S0926-860X(99)00274-4 (Pubitemid 129532985)
    • (1999) Applied Catalysis A: General , vol.189 , Issue.2 , pp. 163-183
    • Sheldon, R.A.1    Downing, R.S.2
  • 6
    • 34047185334 scopus 로고    scopus 로고
    • Palladium nanoparticles as efficient green homogeneous and heterogeneous carbon-carbon coupling precatalysts: A unifying view
    • 10.1021/ic062183h
    • Astruc D., Palladium nanoparticles as efficient green homogeneous and heterogeneous carbon-carbon coupling precatalysts: a unifying view. Inorganic Chemistry 2007 46 1884 1894 10.1021/ic062183h
    • (2007) Inorganic Chemistry , vol.46 , pp. 1884-1894
    • Astruc, D.1
  • 7
    • 34548826220 scopus 로고    scopus 로고
    • In-situ loading of noble metal nanoparticles on hydroxyl-group-rich titania precursor and their catalytic applications
    • DOI 10.1021/cm0714032
    • Zhong L. S., Hu J. S., Cui Z. M., Wan L. J., Song W. G., In-situ loading of noble metal nanoparticles on hydroxyl-group-rich titania precursor and their catalytic applications. Chemistry of Materials 2007 19 4557 4562 10.1021/cm0714032 (Pubitemid 47441895)
    • (2007) Chemistry of Materials , vol.19 , Issue.18 , pp. 4557-4562
    • Zhong, L.-S.1    Hu, J.-S.2    Cui, Z.-M.3    Wan, L.-J.4    Song, W.-G.5
  • 8
    • 0042975158 scopus 로고    scopus 로고
    • Formation of carbon-carbon bonds under catalysis by transition-metal nanoparticles
    • 10.1021/ar020267y
    • Moreno-Manas E., Pleixats R., Formation of carbon-carbon bonds under catalysis by transition-metal nanoparticles. Accounts of Chemical Research 2003 36 638 643 10.1021/ar020267y
    • (2003) Accounts of Chemical Research , vol.36 , pp. 638-643
    • Moreno-Manas, E.1    Pleixats, R.2
  • 9
    • 0037062796 scopus 로고    scopus 로고
    • Size effects of PVP-Pd nanoparticles on the catalytic Suzuki reactions in aqueous solution
    • DOI 10.1021/la011469q
    • Li Y., Boone E., El-Sayed M. A., Size effects of PVP-Pd nanoparticles on the catalytic suzuki reactions in aqueous solution. Langmuir 2002 18 4921 4925 10.1021/la011469q (Pubitemid 35383568)
    • (2002) Langmuir , vol.18 , Issue.12 , pp. 4921-4925
    • Li, Y.1    Boone, E.2    El-Sayed, M.A.3
  • 11
    • 84889817180 scopus 로고    scopus 로고
    • The role of palladium nanoparticles as catalysts for carbon-carbon coupling reactions
    • Djakovitch L., Koehler K., De Vries J. G., The role of palladium nanoparticles as catalysts for carbon-carbon coupling reactions. Nanoparticles and Catalysis 2008 65 303 348
    • (2008) Nanoparticles and Catalysis , vol.65 , pp. 303-348
    • Djakovitch, L.1    Koehler, K.2    De Vries, J.G.3
  • 12
    • 53249140768 scopus 로고    scopus 로고
    • An overview of palladium nanocatalysts: Surface and molecular reactivity
    • 10.1002/ejic.200800569
    • Durand J., Teuma E., Gomez M., An overview of palladium nanocatalysts: surface and molecular reactivity. European Journal of Inorganic Chemistry 2008 2008 3577 3586 10.1002/ejic.200800569
    • (2008) European Journal of Inorganic Chemistry , vol.2008 , pp. 3577-3586
    • Durand, J.1    Teuma, E.2    Gomez, M.3
  • 16
    • 0042528885 scopus 로고    scopus 로고
    • Recent studies on the catalytic activity of titanium, zirconium, and hafnium oxides
    • 10.1081/CR-120015740
    • Salem I., Recent studies on the catalytic activity of titanium, zirconium, and hafnium oxides. Catalysis Reviews 2003 45 205 296 10.1081/CR-120015740
    • (2003) Catalysis Reviews , vol.45 , pp. 205-296
    • Salem, I.1
  • 17
    • 58149302568 scopus 로고    scopus 로고
    • Nanoparticle-supported and magnetically recoverable nickel catalyst: A robust and economic hydrogenation and transfer hydrogenation protocol
    • 2-s2.0-58149302568 10.1039/b815058c
    • Polshettiwar V., Baruwati B., Varma R. S., Nanoparticle-supported and magnetically recoverable nickel catalyst: a robust and economic hydrogenation and transfer hydrogenation protocol. Green Chemistry 2009 11 1 127 131 2-s2.0-58149302568 10.1039/b815058c
    • (2009) Green Chemistry , vol.11 , Issue.1 , pp. 127-131
    • Polshettiwar, V.1    Baruwati, B.2    Varma, R.S.3
  • 19
    • 79956216404 scopus 로고    scopus 로고
    • Nickel nanoparticles in hydrogen transfer reactions
    • Alonso F., Riente P., Yus M., Nickel nanoparticles in hydrogen transfer reactions. Accounts of Chemical Research 2011 44 5 379 391
    • (2011) Accounts of Chemical Research , vol.44 , Issue.5 , pp. 379-391
    • Alonso, F.1    Riente, P.2    Yus, M.3
  • 20
    • 71949117774 scopus 로고    scopus 로고
    • Catalytic functionalization of Indoles in a new dimension
    • 2-s2.0-71949117774 10.1002/anie.200901843
    • Bandini M., Eichholzer A., Catalytic functionalization of Indoles in a new dimension. Angewandte Chemie 2009 48 51 9608 9644 2-s2.0-71949117774 10.1002/anie.200901843
    • (2009) Angewandte Chemie , vol.48 , Issue.51 , pp. 9608-9644
    • Bandini, M.1    Eichholzer, A.2
  • 21
    • 9444250154 scopus 로고    scopus 로고
    • Chemistry and pharmacology of analgesic indole alkaloids from the rubiaceous plant, Mitragyna speciosa
    • DOI 10.1248/cpb.52.916
    • Takayama H., Chemistry and pharmacology of analgesic indole alkaloids from the rubiaceous plant, Mitragyna speciosa. Chemical & Pharmaceutical Bulletin 2004 52 8 916 928 10.1248/cpb.52.916 (Pubitemid 41701864)
    • (2004) Chemical and Pharmaceutical Bulletin , vol.52 , Issue.8 , pp. 916-928
    • Takayama, H.1
  • 22
    • 16244370734 scopus 로고    scopus 로고
    • Design, synthesis and anti-plasmodial evaluation in vitro of new 4-aminoquinoline isatin derivatives
    • DOI 10.1016/j.bmc.2005.02.037
    • Chiyanzu I., Clarkson C., Smith P. J., Lehman J., Gut J., Rosenthal P. J., Chibale K., Design, synthesis and anti-plasmodial evaluation in vitro of new 4-aminoquinoline isatin derivatives. Bioorganic and Medicinal Chemistry 2005 13 9 3249 3261 2-s2.0-16244370734 10.1016/j.bmc.2005.02.037 (Pubitemid 40462126)
    • (2005) Bioorganic and Medicinal Chemistry , vol.13 , Issue.9 , pp. 3249-3261
    • Chiyanzu, I.1    Clarkson, C.2    Smith, P.J.3    Lehman, J.4    Gut, J.5    Rosenthal, P.J.6    Chibale, K.7
  • 24
    • 0036754283 scopus 로고    scopus 로고
    • Synthesis of halogen derivatives of benzo[h]chromene and benzo[a]anthracene with promising antimicrobial activities
    • DOI 10.1016/S0014-827X(02)01263-6, PII S0014827X02012636
    • Khafagy M. M., El-Wahas A. H., Eid F. A., El-Agrody A. M., Synthesis of halogen derivatives of benzo[ h ]chromene and benzo[ a ]anthracene with promising antimicrobial activities. Il Farmaco 2002 57 9 715 722 10.1016/S0014-827X(02)01263-6 (Pubitemid 35287005)
    • (2002) Farmaco , vol.57 , Issue.9 , pp. 715-722
    • Khafagy, M.M.1    Abd El-Wahab, A.H.F.2    Eid, F.A.3    El-Agrody, A.M.4
  • 25
    • 0037326264 scopus 로고    scopus 로고
    • Paraherquamides, brevianamides, and asperparalines: Laboratory synthesis and biosynthesis. An interim report
    • 10.1021/ar020229e
    • Williams R. M., Cox R. J., Paraherquamides, brevianamides, and asperparalines: laboratory synthesis and biosynthesis. An interim report. Accounts of Chemical Research 2003 36 2 127 139 10.1021/ar020229e
    • (2003) Accounts of Chemical Research , vol.36 , Issue.2 , pp. 127-139
    • Williams, R.M.1    Cox, R.J.2
  • 27
    • 27644447403 scopus 로고    scopus 로고
    • Synthesis of (±)-coerulescine and a formal synthesis of (±)-horsfiline
    • DOI 10.1016/j.tetlet.2005.10.015, PII S0040403905022197
    • Chang M. Y., Pai C. L., Kung Y. H., Synthesis of (±)-coerulescine and a formal synthesis of (±)-horsfiline. Tetrahedron Letters 2005 46 49 8463 8465 10.1016/j.tetlet.2005.10.015 (Pubitemid 41566093)
    • (2005) Tetrahedron Letters , vol.46 , Issue.49 , pp. 8463-8465
    • Chang, M.-Y.1    Pai, C.-L.2    Kung, Y.-H.3
  • 28
    • 27644566322 scopus 로고    scopus 로고
    • Enantioselective total syntheses of welwitindolinone A and fischerindoles I and G
    • DOI 10.1021/ja056171r
    • Baran S. P., Richter R. M., Enantioselective total syntheses of welwitindolinone A and fischerindoles I and G. Journal of the American Chemical Society 2005 127 44 15394 15396 10.1021/ja056171r (Pubitemid 41572512)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.44 , pp. 15394-15396
    • Baran, P.S.1    Richter, J.M.2
  • 30
    • 0019407644 scopus 로고
    • Isolation and structure determination of a new marine toxin, neosurugatoxin, from the Japanese ivory shell, Babylonia japonica
    • DOI 10.1016/S0040-4039(01)81920-1
    • Kosuge T., Tsuji K., Hirai K., Yamaguchi K., Okamoto Y., Iitaka T., Isolation and structure determination of a new marine toxin, neosurugatoxin, from the Japanese Ivory Shell, Babylonia japonica. Tetrahedron Letters 1981 22 35 3417 3420 10.1016/S0040-4039(01)81920-1 (Pubitemid 11011690)
    • (1981) Tetrahedron Letters , vol.22 , Issue.35 , pp. 3417-3420
    • Kosuge, T.1    Tsuji, K.2    Hirai, K.3
  • 31
    • 0017079032 scopus 로고
    • Oxindole-3-spiropyrrolidines and -piperidines. Synthesis and local anesthetic activity
    • 10.1021/jm00229a007
    • Kornet M. J., Thio A. P., Oxindole-3-spiropyrrolidines and -piperidines. Synthesis and local anesthetic activity. Journal of Medicinal Chemistry 1976 19 7 892 898 10.1021/jm00229a007
    • (1976) Journal of Medicinal Chemistry , vol.19 , Issue.7 , pp. 892-898
    • Kornet, M.J.1    Thio, A.P.2
  • 32
    • 0029081625 scopus 로고
    • Riluzole prevents MPTP-induced parkinsonism in the rhesus monkey: A pilot study
    • 2-s2.0-0029081625 10.1016/0014-2999(95)00362-O
    • Benazzouz A., Boraud T., Dubedat P., Boireau A., Stutzmann J. M., Gross C., Riluzole prevents MPTP-induced parkinsonism in the rhesus monkey: a pilot study. European Journal of Pharmacology 1995 284 3 299 307 2-s2.0-0029081625 10.1016/0014-2999(95)00362-O
    • (1995) European Journal of Pharmacology , vol.284 , Issue.3 , pp. 299-307
    • Benazzouz, A.1    Boraud, T.2    Dubedat, P.3    Boireau, A.4    Stutzmann, J.M.5    Gross, C.6
  • 36
    • 0025967888 scopus 로고
    • Novel, potent aldose reductase inhibitors: 3,4-Dihydro-4-oxo-3-[[5- (trifluoromethyl)-2-benzothiazolyl]methyl]-1- phthalazine-acetic acid (zopolrestat) and congeners
    • 2-s2.0-0025967888
    • Mylari B. L., Larson E. R., Beyer T. A., Zembrowski W. J., Aldinger C. E., Dee M. F., Siegel T. W., Singleton D. H., Novel, potent aldose reductase inhibitors: 3,4-Dihydro-4-oxo-3-[[5-(trifluoromethyl)-2-benzothiazolyl]methyl]- 1- phthalazine-acetic acid (zopolrestat) and congeners. Journal of Medicinal Chemistry 1991 34 1 108 122 2-s2.0-0025967888
    • (1991) Journal of Medicinal Chemistry , vol.34 , Issue.1 , pp. 108-122
    • Mylari, B.L.1    Larson, E.R.2    Beyer, T.A.3    Zembrowski, W.J.4    Aldinger, C.E.5    Dee, M.F.6    Siegel, T.W.7    Singleton, D.H.8
  • 37
    • 0031812701 scopus 로고    scopus 로고
    • Thiazolyl and benzothiazolyl Schiff bases as novel possible lipoxygenase inhibitors and anti inflammatory agents. Synthesis and biological evaluation
    • Hadjipavlou-Litina D. J., Geronikaki A. A., Thiazolyl and benzothiazolyl Schiff bases as novel possible lipoxygenase inhibitors and anti inflammatory agents. Synthesis and biological evaluation. Drug Design and Discovery 1998 15 3 199 206 2-s2.0-0031812701 (Pubitemid 28302002)
    • (1998) Drug Design and Discovery , vol.15 , Issue.3 , pp. 199-206
    • Hadjipavlou-Litina, D.J.1    Geronikaki, A.A.2
  • 39
    • 0035833071 scopus 로고    scopus 로고
    • Biological evaluation of hepatitis C virus helicase inhibitors
    • DOI 10.1016/S0960-894X(01)00263-3, PII S0960894X01002633
    • Phoon C. W., Ng P. Y., Ting A. E., Yeo S. L., Sim M. M., Biological evaluation of hepatitis c virus helicase inhibitors. Bioorganic & Medicinal Chemistry Letters 2001 11 13 1647 1650 10.1016/S0960-894X(01)00263-3 (Pubitemid 32568288)
    • (2001) Bioorganic and Medicinal Chemistry Letters , vol.11 , Issue.13 , pp. 1647-1650
    • Phoon, C.W.1    Ng, P.Y.2    Ting, A.E.3    Yeo, S.L.4    Sim, M.M.5
  • 42
    • 0017615948 scopus 로고
    • 3 Halo 5,7 dimethylpyrazolo[1,5 a]pyrimidines, a nonbenzodiazepinoid class of antianxiety agents devoid of potentiation of central nervous system depressant effects of ethanol or barbiturates
    • Krikpatrick W. E., Okabe T., Hillyard I. W., Robins R. K., Dren A. T., 3-Halo-5,7-dimethylpyrazolo[1,5-A]pyrimidines, a nonbenzodiazepinoid class of antianxiety agents devoid of potentiation of central nervous system depressant effects of ethanol or barbiturates. Journal of Medicinal Chemistry 1977 20 3 386 393 10.1021/jm00213a014 (Pubitemid 8050630)
    • (1977) Journal of Medicinal Chemistry , vol.20 , Issue.3 , pp. 386-393
    • Kirkpatrick, W.E.1    Okabe, T.2    Hillyard, I.W.3
  • 43
    • 0023149797 scopus 로고
    • Reactions with 4-(cyanoacetyl)phenazone: Synthesis of novel thiazole, hydrazinopyrazole and pyrazolo[5.1-c][1.2.4]triazine derivatives
    • DOI 10.1002/ardp.19873200311
    • Elagamy A. A., El-Taweel F. M. A., Amer F. A., Zoorob H. H., Reactions with 4-(Cyanoacetyl)phenazone: synthesis of novel thiazole, hydrazinopyrazole and pyrazolo[5.1-c][1.2.4]triazine derivatives. Archiv der Pharmazie 1987 320 3 246 252 10.1002/ardp.19873200311 (Pubitemid 17023029)
    • (1987) Archiv der Pharmazie , vol.320 , Issue.3 , pp. 246-252
    • Elagamey, A.G.A.1    El Taweel, F.A.2
  • 44
    • 0036008105 scopus 로고    scopus 로고
    • Control of the reaction between 2-aminobenzothiazoles and mannich bases. Synthesis of pyrido[2,1-b][1,3]benzothiazoles versus [1,3]benzothiazolo[2,3-b] quinazolines
    • Nogueras M., Low J. N., Quiroga J., Hernández P., Insuasty B., Abonía R., Cobo J., Sánchez A., Control of the reaction between 2-aminobenzothiazoles and Mannich bases. Synthesis of pyrido[2,1- b ][1,3]benzothiazoles versus [1,3]benzothiazolo[2,3- b ]quinazolines. Journal of the Chemical Society, Perkin Transactions 1 2002 4 555 559 10.1039/B109676A (Pubitemid 35188294)
    • (2002) Journal of the Chemical Society. Perkin Transactions 1 , Issue.4 , pp. 555-559
    • Quiroga, J.1    Hernandez, P.2    Insuasty, B.3    Abonia, R.4    Cobo, J.5    Sanchez, A.6    Nogueras, M.7    Low, J.N.8
  • 45
    • 0037203997 scopus 로고    scopus 로고
    • Antitumor benzothiazoles. 16. Synthesis and pharmaceutical properties of antitumor 2-(4-aminophenyl)benzothiazole amino acid prodrugs
    • DOI 10.1021/jm011025r
    • Hutchinson I., Jennings S. A., Vishnuvajjala B. R., Westwell A. D., Stevens M. F. G., Antitumor benzothiazoles. 16. Synthesis and pharmaceutical properties of antitumor 2-(4-aminophenyl)benzothiazole amino acid prodrugs. Journal of Medicinal Chemistry 2002 45 3 744 747 2-s2.0-0037203997 10.1021/jm011025r (Pubitemid 34145721)
    • (2002) Journal of Medicinal Chemistry , vol.45 , Issue.3 , pp. 744-747
    • Hutchinson, I.1    Jennings, S.A.2    Vishnuvajjala, B.R.3    Westwell, A.D.4    Stevens, M.F.G.5
  • 46
    • 70749097429 scopus 로고    scopus 로고
    • Synthesis of 4-benzyl-1,3-thiazole derivatives as potential anti-inflammatory agents: An analogue-based drug design approach
    • 10.1080/14756360802519558
    • Sharma R. N., Xavier F. P., Vasu K. K., Chaturvedi S. C., Pancholi S. S., Synthesis of 4-benzyl-1,3-thiazole derivatives as potential anti-inflammatory agents: an analogue-based drug design approach. Journal of Enzyme Inhibition and Medicinal Chemistry 2009 24 890 897 10.1080/14756360802519558
    • (2009) Journal of Enzyme Inhibition and Medicinal Chemistry , vol.24 , pp. 890-897
    • Sharma, R.N.1    Xavier, F.P.2    Vasu, K.K.3    Chaturvedi, S.C.4    Pancholi, S.S.5
  • 47
    • 0242656243 scopus 로고    scopus 로고
    • Multi-Component Synthesis of Pyran-Annulated Thiazoles under Solvent-Free Microwave Irradiation
    • Yadav L. D. S., Singh A., Multi-component synthesis of pyran-annulated thiazoles under solvent-free microwave irradiation. Synthesis 2003 15 2395 2399 2-s2.0-0242656243 (Pubitemid 37409989)
    • (2003) Synthesis , Issue.15 , pp. 2395-2399
    • Yadav, L.D.S.1    Singh, A.2
  • 50
    • 0031373811 scopus 로고    scopus 로고
    • Synthesis of novel spiro[indole-pyranoimidazole] and spiro[indolepyranopyrrole]derivatives
    • Dandia A., Taneja H., Saha M., Synthesis of novel spiro[indole- pyranoimidazole] and spiro[indolepyranopyrrole]derivatives. Indian Journal of Chemical Technology 1997 4 5 243 246 2-s2.0-0031373811 (Pubitemid 127690879)
    • (1997) Indian Journal of Chemical Technology , vol.4 , Issue.5 , pp. 243-246
    • Dandia, A.1    Taneja, H.2    Saha, M.3
  • 51
    • 0032915778 scopus 로고    scopus 로고
    • An efficient procedure for the synthesis of spiro [3H-indole-3,4' (1'H) pyrano [2,3-C] pyrrole]-5'-carbonitriles using solid inorganic supports and microwave activation
    • Dandia A., Taneja H., Gupta R., Paul S., An efficient procedure for the synthesis of spiro [3H-indole-3,4' (1'H) pyrano [2,3-C] pyrrole]-5'- carbonitriles using solid inorganic supports and microwave activation. Synthetic Communications 1999 29 13 2323 2335 2-s2.0-0032915778 (Pubitemid 29227708)
    • (1999) Synthetic Communications , vol.29 , Issue.13 , pp. 2323-2335
    • Dandia, A.1    Taneja, H.2    Gupta, R.3    Paul, S.4
  • 52
    • 84861073326 scopus 로고    scopus 로고
    • Lithium-Acetate-Mediated Biginelli One-Pot Multicomponent Synthesis under Solvent-Free Conditions and Cytotoxic Activity against the Human Lung Cancer Cell Line A549 and Breast Cancer Cell LineMCF7
    • 10.1100/2012/109432 109432
    • Sachdeva H., Dwivedi D., Lithium-Acetate-Mediated Biginelli One-Pot Multicomponent Synthesis under Solvent-Free Conditions and Cytotoxic Activity against the Human Lung Cancer Cell Line A549 and Breast Cancer Cell LineMCF7. The Scientific World Journal 2012 2012 9 10.1100/2012/109432 109432
    • (2012) The Scientific World Journal , vol.2012 , pp. 9
    • Sachdeva, H.1    Dwivedi, D.2
  • 53
    • 84864411347 scopus 로고    scopus 로고
    • Comparative studies of lewis acidity of alkyl-tin chlorides in multicomponent biginelli condensation using grindstone chemistry technique
    • 10.4067/S0717-97072012000100013
    • Sachdeva H., Saroj R., Khaturia S., Singh H. L. J., Comparative studies of lewis acidity of alkyl-tin chlorides in multicomponent biginelli condensation using grindstone chemistry technique. Journal of the Chilean Chemical Society 2012 57 1 1012 1016 10.4067/S0717-97072012000100013
    • (2012) Journal of the Chilean Chemical Society , vol.57 , Issue.1 , pp. 1012-1016
    • Sachdeva, H.1    Saroj, R.2    Khaturia, S.3    Singh, H.L.J.4
  • 54
    • 0034847191 scopus 로고    scopus 로고
    • Microwave assisted one pot synthesis of a series of trifluoromethyl substituted spiro [indole-triazoles]
    • DOI 10.1016/S0022-1139(01)00429-8, PII S0022113901004298
    • Dandia A., Singh R., Sachdeva H., Arya K., Microwave assisted one pot synthesis of a series of trifluoromethyl substituted spiro [indole-triazoles]. Journal of Fluorine Chemistry 2001 111 1 61 67 2-s2.0-0034847191 10.1016/S0022-1139(01)00429-8 (Pubitemid 33623135)
    • (2001) Journal of Fluorine Chemistry , vol.111 , Issue.1 , pp. 61-67
    • Dandia, A.1    Singh, R.2    Sachdeva, H.3    Arya, K.4
  • 55
    • 0034897197 scopus 로고    scopus 로고
    • Improved synthesis of 3-spiro indolines in dry media under microwave irradiation
    • DOI 10.1081/SCC-100104339
    • Dandia A., Sachdeva H., Singh R., Improved synthesis of 3-spiro indolines in dry media under microwave irradiation. Synthetic Communications 2001 31 12 1879 1892 2-s2.0-0034897197 10.1081/SCC-100104339 (Pubitemid 32709071)
    • (2001) Synthetic Communications , vol.31 , Issue.12 , pp. 1879-1892
    • Dandia, A.1    Sachdeva, H.2    Singh, R.3
  • 56
    • 29144497343 scopus 로고    scopus 로고
    • Microwave promoted and improved thermal synthesis of spiro[indole- pyranobenzopyrans] and spiro[indole-pyranoimidazoles]
    • Dandia A., Singh R., Sachdeva H., Gupta R., Paul S., Microwave promoted and improved thermal synthesis of spiro[indole-pyranobenzopyrans] and spiro[indole-pyranoimidazoles]. Journal of the Chinese Chemical Society 2003 50 2 273 278 2-s2.0-29144497343 (Pubitemid 43658549)
    • (2003) Journal of the Chinese Chemical Society , vol.50 , Issue.2 , pp. 273-278
    • Dandia, A.1    Singh, R.2    Sachdeva, H.3    Gupta, R.4    Paul, S.5
  • 57
    • 0033853091 scopus 로고    scopus 로고
    • Montmorillonite catalysed synthesis of novel spiro[3H-indole-3,3′- [3H-1,2,4] triazol]-2(1 H) ones in dry media under microwave irradiation
    • 10.3184/030823400103167471
    • Dandia A., Sachdeva H., Singh R., Montmorillonite catalysed synthesis of novel spiro[3H-indole-3,3′- [3H-1,2,4] triazol]-2(1 H) ones in dry media under microwave irradiation. Journal of Chemical Research 2000 2000 6 272 275 10.3184/030823400103167471
    • (2000) Journal of Chemical Research , vol.2000 , Issue.6 , pp. 272-275
    • Dandia, A.1    Sachdeva, H.2    Singh, R.3
  • 58
    • 0019201671 scopus 로고
    • Spiro heterocyclic compounds III. Synthesis of spiro [oxindole-3,4'-(4'H- pyran)] compounds
    • Higashiyama K., Otomasu H., Spiro heterocyclic compounds. III. Synthesis of spiro[oxindole-3, 4′-(4′H-pyran)] compounds. Chemical & Pharmaceutical Bulletin 1980 28 2 648 651 10.1248/cpb.28.648 (Pubitemid 11236588)
    • (1980) Chemical and Pharmaceutical Bulletin , vol.28 , Issue.2 , pp. 648-651
    • Higashiyama, K.1    Otomasu, H.2
  • 59
    • 0023803169 scopus 로고
    • Studies in spiro-heterocycles. Part-XII. Synthesis of some fluorine containing spiro[3 H -indole-3,4(4 H)-pyrano[2,3- d ]pyrimidine]-2,5,7(1 H)-triones as CNS agents
    • Joshi K. C., Jain R., Sharma K., Bhattacharya S. K., Goel R. K., Studies in spiro-heterocycles. Part-XII. Synthesis of some fluorine containing spiro[3 H -indole-3,4(4 H)-pyrano[2,3- d ]pyrimidine]-2,5,7(1 H)-triones as CNS agents. Journal of the Indian Chemical Society 1988 115 202 204
    • (1988) Journal of the Indian Chemical Society , vol.115 , pp. 202-204
    • Joshi, K.C.1    Jain, R.2    Sharma, K.3    Bhattacharya, S.K.4    Goel, R.K.5
  • 60
    • 0037231715 scopus 로고    scopus 로고
    • Microwave assisted one pot synthesis of novel 11-amino-3-phenyl-2-thioxo- 10-oxo-imidazolo[5",4":5′,6′] pyrano[4′,3′: 3,4]furo[2,3-b]indoles
    • Dandia A., Sachdeva H., Singh R., Sharma C. S., Microwave assisted one pot synthesis of novel 11-amino-3-phenyl-2-thioxo-10-oxo- imidazolo[5"4":5′6′] pyrano[4′3′: 3,4]furo[2,3-b]indoles. Indian Journal of Chemistry B 2003 42 140 144
    • (2003) Indian Journal of Chemistry B , vol.42 , pp. 140-144
    • Dandia, A.1    Sachdeva, H.2    Singh, R.3    Sharma, C.S.4
  • 61
    • 30644463099 scopus 로고    scopus 로고
    • Solution-processed zinc oxide field-effect transistors based on self-assembly of colloidal nanorods
    • DOI 10.1021/nl051586w
    • Sun B., Sirringhaus H., Solution-processed zinc oxide field-effect transistors based on self-assembly of colloidal nanorods. Nano Letters 2005 5 12 2408 2413 2-s2.0-30644463099 10.1021/nl051586w (Pubitemid 43088886)
    • (2005) Nano Letters , vol.5 , Issue.12 , pp. 2408-2413
    • Sun, B.1    Sirringhaus, H.2
  • 62
    • 33847610261 scopus 로고    scopus 로고
    • Preparation and characterization of NiO nanoparticles through calcination of malate gel
    • DOI 10.1016/j.matlet.2006.07.113, PII S0167577X06008998
    • Li Q., Wang L. S., Hu B. Y., Yang C., Zhou L., Zhang L., Preparation and characterization of NiO nanoparticles through calcination of malate gel. Materials Letters 2007 61 8-9 1615 1618 2-s2.0-33847610261 10.1016/j.matlet. 2006.07.113 (Pubitemid 46367240)
    • (2007) Materials Letters , vol.61 , Issue.8-9 , pp. 1615-1618
    • Li, Q.1    Wang, L.-S.2    Hu, B.-Y.3    Yang, C.4    Zhou, L.5    Zhang, L.6
  • 63
    • 77951673939 scopus 로고    scopus 로고
    • Ultrasound-induced in situ formation of coordination organogels from isobutyric acids and zinc oxide nanoparticles
    • 2-s2.0-77951673939 10.1021/la903923q
    • Kotal A., Paira T. K., Banerjee S., Mandal T. K., Ultrasound-induced in situ formation of coordination organogels from isobutyric acids and zinc oxide nanoparticles. Langmuir 2010 26 9 6576 6582 2-s2.0-77951673939 10.1021/la903923q
    • (2010) Langmuir , vol.26 , Issue.9 , pp. 6576-6582
    • Kotal, A.1    Paira, T.K.2    Banerjee, S.3    Mandal, T.K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.