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Volumn 16, Issue 1, 2012, Pages 121-128

Magnetic nanoparticles catalyzed synthesis of diverse N-Heterocycles

Author keywords

Diverse synthesis; Fe 3O 4 nanoparticles; Magnetically separable; Multicomponent reactions (MCRs); N heterocycles

Indexed keywords

INDOLE DERIVATIVE; IRON OXIDE; MAGNETIC NANOPARTICLE; PYRANO[2,3 D]PYRIMIDINE DERIVATIVE; PYRIDO[2,3 D] PYRIMIDINE DERIVATIVE; PYRIMIDINE DERIVATIVE; SPIROOXINDOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84858699776     PISSN: 13811991     EISSN: 1573501X     Source Type: Journal    
DOI: 10.1007/s11030-011-9336-z     Document Type: Article
Times cited : (70)

References (32)
  • 1
    • 0034678033 scopus 로고    scopus 로고
    • Target-Oriented and Diversity-Oriented Organic Synthesis Discovery
    • doi:10.1126/science.287.5460.1964
    • Schreiber SL (2000) Target-Oriented and Diversity-Oriented Organic Synthesis Discovery. Science 287: 1964-1969. doi:10.1126/science.287.5460.1964
    • (2000) Science , vol.287 , pp. 1964-1969
    • Schreiber, S.L.1
  • 2
    • 31544434530 scopus 로고    scopus 로고
    • Recent developments in isocyanide based multicomponent reactions in applied chemistry
    • doi:10.1021/cr0505728
    • Dömling A (2006) Recent developments in isocyanide based multicomponent reactions in applied chemistry.ChemRev 106: 17-89. doi:10.1021/cr0505728
    • (2006) ChemRev , vol.106 , pp. 17-89
    • Dömling, A.1
  • 3
    • 77950587501 scopus 로고    scopus 로고
    • 4nanoparticles: A robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine
    • doi:10.1039/B920000B
    • 4nanoparticles: a robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine. Green Chem 12: 570-573. doi:10.1039/B920000B
    • (2010) Green Chem , vol.12 , pp. 570-573
    • Zeng, T.1    Chen, W.W.2    Ciprian Cirtiu, M.3    Moores, A.4    Song, G.5    Li, C.-J.6
  • 4
    • 63549098104 scopus 로고    scopus 로고
    • Superparamagnetic iron oxide as an efficient catalyst for the one-pot, solvent-free synthesis of α-aminonitriles
    • doi:10. 1016/j.tetlet.2009.02.199
    • Mojtahedi MM, Abaee MS, Alishiri T (2009) Superparamagnetic iron oxide as an efficient catalyst for the one-pot, solvent-free synthesis of α-aminonitriles. Tetrahedron Lett 50: 2322-2325. doi:10. 1016/j.tetlet.2009.02.199
    • (2009) Tetrahedron Lett , vol.50 , pp. 2322-2325
    • Mojtahedi, M.M.1    Abaee, M.S.2    Alishiri, T.3
  • 5
    • 0041846627 scopus 로고    scopus 로고
    • Applications of magnetic nanoparticles in biomedicine
    • doi:10.1088/0022-3727/36/13/201
    • Pankhurst QA, Connolly J, Jones SK, Dobson J (2003) Applications of magnetic nanoparticles in biomedicine. J Phys 6: R167-R181. doi:10.1088/0022- 3727/36/13/201
    • (2003) J Phys , vol.6
    • Pankhurst, Q.A.1    Connolly, J.2    Jones, S.K.3    Dobson, J.4
  • 6
    • 0041931064 scopus 로고    scopus 로고
    • Viral-induced self-assembly of magnetic nanoparticles allows the detection of viral particles in biological media
    • DOI 10.1021/ja036409g
    • Perez JM, Simeone FJ, Salki Y, Josephson L, Weissleder R (2003) Viral-induced self-assembly of magnetic nanoparticles allows the detection of viral particles in biological media. J Am Chem Soc 125: 10192-10193. doi:10.1021/ja036409g (Pubitemid 37022228)
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.34 , pp. 10192-10193
    • Perez, J.M.1    Simeone, F.J.2    Saeki, Y.3    Josephson, L.4    Weissleder, R.5
  • 8
    • 0027248862 scopus 로고
    • Positive inotropic activity of 5-amino-6-cyano-1,3-dimethyl-1,2,3,4- tetrahydropyrido[2,3-d]pyrimidine -2,4-dione in cardiac muscle from guinea-pig and man. Part 6: Compounds with positive inotropic activity
    • Heber D, Heers C, Ravens U (1993) Positive inotropic activity of 5-amino-6-cyano-1,3-dimethyl-1,2,34-tetrahydropyrido[2,3-d] pyrimidine-2,4-dione in cardiac muscle from guinea-pig and man. Part 6: compounds with positive inotropic activity. Pharmazie 48: 537-541 (Pubitemid 23258217)
    • (1993) Pharmazie , vol.48 , Issue.7 , pp. 537-541
    • Heber, D.1    Heers, R.C.U.2
  • 9
    • 0018874182 scopus 로고
    • Synthesis and antitumor activity of 2,4-diamino-6-(2,5-dimethoxybenzyl)- 5-methylpyrido[2,3-d]pyrimidine
    • Griva EM, Lee S, Siyal CW, Duch DS, Nichol CA (1980) Synthesis and antitumor activity of 2,4-diamino-6-(2,5-dimethoxybenzyl)- 5-methylpyrido[2,3-d] pyrimidine. JMed Chem 23: 327-329. doi:10.1021/jm00177a025 (Pubitemid 10129981)
    • (1980) Journal of Medicinal Chemistry , vol.23 , Issue.3 , pp. 327-329
    • Grivsky, E.M.1    Lee, S.2    Sigel, C.W.3
  • 10
    • 0032223331 scopus 로고    scopus 로고
    • Synthesis and antibacterial properties of new dithienyl containing pyran, pyrano[2,3-b] pyridine, pyrano[2,3-d]pyrimidine and pyridine derivatives
    • Ghorab MM, Hassan AY (1998) synthesis and antibacterial properties of new dithienyl containing pyran, pyrano[2,3-b] pyridine, pyrano[2,3-d]pyrimidine and pyridine derivatives. Phosphorus Sulfur Silicon Relat Elem 141: 251-261. doi:10.1080/10426509808033737 (Pubitemid 128396178)
    • (1998) Phosphorus, Sulfur and Silicon and Related Elements , vol.141 , pp. 251-261
    • Ghorab, M.M.1    Hassan, A.Y.2
  • 11
    • 70349759169 scopus 로고
    • Pyrido[2,3-d]pyrimidines and their use as endothelin antagonists
    • Eur Patent 608565
    • Furuya S, Ohtaki T (1994) Pyrido[2,3-d]pyrimidines and their use as endothelin antagonists. Eur Patent 608565
    • (1994)
    • Furuya, S.1    Ohtaki, T.2
  • 12
    • 70349760363 scopus 로고
    • Preparation of pyrimidopyrimidine derivatives useful as bronchodilators, vasodilators, antiallergic
    • Eur Patent 351058
    • Coates WJ (1990) Preparation of pyrimidopyrimidine derivatives useful as bronchodilators, vasodilators, antiallergic. Eur Patent 351058
    • (1990)
    • Coates, W.J.1
  • 13
    • 70349780206 scopus 로고
    • Pyrimidopyrimidinedione derivatives and their use as antiallergic agent
    • Eur Patent 163599
    • KitamuraNA,Onishi (1984) Pyrimidopyrimidinedione derivatives and their use as antiallergic agent. Eur Patent 163599
    • (1984)
    • Kitamura, N.A.1    Onishi2
  • 14
    • 0015380521 scopus 로고
    • Antimalarial substances. 26. Folate antagonists. 4. Antimalarial and antimetabolite effects of 2,4-diamino-6-[(benzyl)amino]pyrido[2,3-d]pyrimidines
    • doi:10.1021/jm00278a009
    • Davoll J, Clarke J, Elslager EF (1972) Antimalarial substances. 26. Folate antagonists. 4. Antimalarial and antimetabolite effects of 2,4-diamino-6-[(benzyl)amino]pyrido[2,3-d]pyrimidines. J Med Chem 15: 837-839. doi:10.1021/jm00278a009
    • (1972) J Med Chem , vol.15 , pp. 837-839
    • Davoll, J.1    Clarke, J.2    Elslager, E.F.3
  • 15
    • 70349779012 scopus 로고
    • Herbicidal sulfonamides
    • US Patent 4339267
    • Levitt G (1982) Herbicidal sulfonamides. US Patent 4339267
    • (1982)
    • Levitt, G.1
  • 16
    • 1842481396 scopus 로고    scopus 로고
    • Effective Synthesis of 7-Amino-6-cyano-5-aryl-5H-pyrano[2,3-d]pyrimidine- 2,4(1H,3H)-diones under Microwave Irradiation
    • DOI 10.1081/SCC-120030318
    • GaoY, Tu SJ, Li T, ZhangX, Zhu S, Fang F, ShiD (2004) Effective synthesis of 7-Amino-6-cyano-5-aryl-5H-pyrano[2,3-d]pyrimidine- 2,4(1H,3H)-diones under microwave irradiation. Synth Commun 34: 1295-1299. doi:10.1081/SCC-120030318 (Pubitemid 38452259)
    • (2004) Synthetic Communications , vol.34 , Issue.7 , pp. 1295-1299
    • Gao, Y.1    Tu, S.2    Li, T.3    Zhang, X.4    Zhu, S.5    Fang, F.6    Shi, D.7
  • 17
    • 28844505081 scopus 로고    scopus 로고
    • Green synthesis of pyrano[2,3-d]-pyrimidine derivatives in ionic liquids
    • DOI 10.1080/00397910500282661
    • Yu J, Wang H (2005) Green synthesis of pyrano [2,3-d]-pyrimidine derivatives in ionic liquids. Synth Commun 35: 3133-3140. doi:10.1080/ 00397910500282661 (Pubitemid 41769829)
    • (2005) Synthetic Communications , vol.35 , Issue.24 , pp. 3133-3140
    • Yu, J.1    Wang, H.2
  • 18
    • 0141957353 scopus 로고    scopus 로고
    • A novel three-component one-pot synthesis of pyrano[2,3-d]pyrimidines and pyrido[2,3-d]pyrimidines using microwave heating in the solid state
    • DOI 10.1016/j.tetlet.2003.09.063
    • Devi I, Kumar BSD, Bhuyan PJ (2003) A novel three-component one-pot synthesis of pyrano[2,3-d]pyrimidines and pyrido [2,3-d]pyrimidines using microwave heating in the solid state. Tetrahedron Lett 44: 8307-8310. doi:10.1016/j.tetlet.2003.09.063 (Pubitemid 37238975)
    • (2003) Tetrahedron Letters , vol.44 , Issue.45 , pp. 8307-8310
    • Devi, I.1    Kumar, B.S.D.2    Bhuyan, P.J.3
  • 19
    • 50849139874 scopus 로고    scopus 로고
    • Diammonium hydrogen phosphate as a versatile and efficient catalyst for the one-pot synthesis of pyrano[2,3- d ]pyrimidinone derivatives in aqueous media
    • doi:10.1007/s11030-008-9079-7
    • Balalaie S, Abdolmohammadi S, Bijanzadeh HR, Amani AM (2008) Diammonium hydrogen phosphate as a versatile and efficient catalyst for the one-pot synthesis of pyrano[2,3- d ]pyrimidinone derivatives in aqueous media. Mol Divers 12: 85-91. doi:10.1007/s11030-008-9079-7
    • (2008) Mol Divers , vol.12 , pp. 85-91
    • Balalaie, S.1    Abdolmohammadi, S.2    Bijanzadeh, H.R.3    Amani, A.M.4
  • 20
    • 79957548242 scopus 로고    scopus 로고
    • Application of mobilized Cu-nanoparticles as heterogeneous catalyst for the synthesis of a-amino phosphonates via A2-P coupling
    • doi:10.1039/c0cy00060d
    • Kidwai M, Bhardwaj S, Mishra NK, Jain A, Kumar A, Mozzumdar S (2011) Application of mobilized Cu-nanoparticles as heterogeneous catalyst for the synthesis of a-amino phosphonates via A2-P coupling. Catal Sci Technol. doi:10.1039/c0cy00060d
    • (2011) Catal Sci Technol
    • Kidwai, M.1    Bhardwaj, S.2    Mishra, N.K.3    Jain, A.4    Kumar, A.5    Mozzumdar, S.6
  • 21
    • 79955048496 scopus 로고    scopus 로고
    • Bis[(L)prolinato- N,O]Zn in acetic acid-water: A novel catalytic system for the synthesis of β-amino carbonyls via Mannich reaction at room temperature
    • doi:10.1002/aoc.1764
    • Kidwai M, Jain A, Poddar R, Bhardwaj S (2011) Bis[(L)prolinato- N,O]Zn in acetic acid-water: a novel catalytic system for the synthesis of β-amino carbonyls via Mannich reaction at room temperature. Appl Organomet Chem 25: 335-340. doi:10.1002/aoc.1764
    • (2011) Appl Organomet Chem , vol.25 , pp. 335-340
    • Kidwai, M.1    Jain, A.2    Poddar, R.3    Bhardwaj, S.4
  • 22
    • 79651473007 scopus 로고    scopus 로고
    • 1,4-addition of terminal alkynes to conjugated enones in water using green catalyst Bis[(L)prolinato-N,O]Zn - An environmentally benign protocol
    • doi:10.1007/s10562-010-0451-8
    • Kidwai M, Jain A, Bhardwaj S (2011) 1,4-addition of terminal alkynes to conjugated enones in water using green catalyst Bis[(L)prolinato-N,O]Zn - an environmentally benign protocol. Catal Lett 141: 183-190. doi:10.1007/s10562- 010-0451-8
    • (2011) Catal Lett , vol.141 , pp. 183-190
    • Kidwai, M.1    Jain, A.2    Bhardwaj, S.3
  • 23
    • 79955070976 scopus 로고    scopus 로고
    • Zn[(L)Proline]2 in water: A new easily accessible and recyclable catalytic system for the synthesis of pyrazoles
    • doi:10.1016/j.jorganchem.2010.09.012
    • Kidwai M, Jain A, Poddar R (2011) Zn[(L)Proline]2 in water: a new easily accessible and recyclable catalytic system for the synthesis of pyrazoles. J Organomet Chem 696: 1939-1944. doi:10.1016/j.jorganchem.2010.09.012
    • (2011) J Organomet Chem , vol.696 , pp. 1939-1944
    • Kidwai, M.1    Jain, A.2    Poddar, R.3
  • 26
    • 3142777194 scopus 로고    scopus 로고
    • Preparation and characterization of (3-aminopropyl) triethoxysilane- coated magnetite nanoparticles
    • doi:10.1016/j.jmmm.2004.01.094
    • Yamaura M, Camilo RL, Sampaio LC, Macedo MA, Nakamura M, Toma HE (2004) Preparation and characterization of (3-aminopropyl) triethoxysilane-coated magnetite nanoparticles. J Magn Magn Mater 279:210-217. doi:10.1016/j.jmmm.2004. 01.094
    • (2004) J Magn Magn Mater , vol.279 , pp. 210-217
    • Yamaura, M.1    Camilo, R.L.2    Sampaio, L.C.3    Macedo, M.A.4    Nakamura, M.5    Toma, H.E.6
  • 27
    • 0037326264 scopus 로고    scopus 로고
    • Paraherquamides, brevianamides, and asperparalines: Laboratory synthesis and biosynthesis. An interim report
    • doi:10.1021/ar020229e
    • Williams RM, Cox R (2003) Paraherquamides, brevianamides, and asperparalines: laboratory synthesis and biosynthesis. An interim report. Acc Chem Res 36:127-139. doi:10.1021/ar020229e
    • (2003) Acc Chem Res , vol.36 , pp. 127-139
    • Williams, R.M.1    Cox, R.2
  • 28
    • 36749025633 scopus 로고    scopus 로고
    • Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents
    • DOI 10.1002/anie.200701342
    • Galliford CV, Scheidt KA (2007) Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents. Angew Chem Int Ed 46: 8748-8758. doi:10.1002/anie.200701342 (Pubitemid 350207923)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.46 , pp. 8748-8758
    • Galliford, C.V.1    Scheidt, K.A.2
  • 29
    • 34547586034 scopus 로고    scopus 로고
    • A simple and clean procedure for three-component synthesis of spirooxindoles in aqueous medium
    • DOI 10.1016/j.tet.2007.06.113, PII S004040200701191X
    • Zhu S-L, Ji S-J, Zhang Y (2007) A simple and clean procedure for three-component synthesis of spirooxindoles in aqueous medium. Tetrahedron 63: 9365-9372. doi:10.1016/j.tet.2007.06.113 (Pubitemid 47198700)
    • (2007) Tetrahedron , vol.63 , Issue.38 , pp. 9365-9372
    • Zhu, S.-L.1    Ji, S.-J.2    Zhang, Y.3
  • 30
    • 77949397767 scopus 로고    scopus 로고
    • Efficient one pot synthesis of spirooindole derivatives catalyzed by L-Proline in aqueous medium
    • doi:10.1021/cc9001185
    • Li Y, Chen H, Shi C, Shi, Ji S (2010) Efficient one pot synthesis of spirooindole derivatives catalyzed by L-Proline in aqueous medium. J Comb Chem 12: 231-237. doi:10.1021/cc9001185
    • (2010) J Comb Chem , vol.12 , pp. 231-237
    • Li, Y.1    Chen, H.2    Shi, C.3    Shi4    Ji, S.5
  • 31
    • 33846382304 scopus 로고    scopus 로고
    • 3-catalyzed, facile and efficient method for the synthesis of spirooxaindoles under conventional and solvent-free microwave conditions
    • doi:10.1016/j.tet.2006.12.042
    • 3-catalyzed, facile and efficient method for the synthesis of spirooxaindoles under conventional and solvent-free microwave conditions. Tetrahedron 63: 2057-2063. doi:10.1016/j.tet.2006.12.042
    • (2007) Tetrahedron , vol.63 , pp. 2057-2063
    • Shanthi, G.1    Subbulakshmi, G.2    Perumal, P.T.3
  • 32
    • 58149302568 scopus 로고    scopus 로고
    • Nanoparticle-supported and magnetically recoverable nickel catalyst: A robust and economic hydrogenation and transfer hydrogenation protocol
    • doi:10.1039/b815058c
    • Polshettiwar V, Baruwati B, Varma RS (2009) Nanoparticle-supported and magnetically recoverable nickel catalyst: a robust and economic hydrogenation and transfer hydrogenation protocol. Green Chem 11: 127-131. doi:10.1039/b815058c
    • (2009) Green Chem , vol.11 , pp. 127-131
    • Polshettiwar, V.1    Baruwati, B.2    Varma, R.S.3


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