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Volumn 21, Issue 1, 2013, Pages

Three-component synthesis of pyrano[2,3-d]-pyrimidine dione derivatives facilitated by sulfonic acid nanoporous silica (SBA-Pr- SO§ssub§3§esub§H) and their docking and urease inhibitory activity

Author keywords

Barbituric acid; Multicomponent reaction (MCRs); Pyrano 2,3 d pyrimidine diones; SBA Pr SOH; Urease inhibitory

Indexed keywords

7 AMINO 6 CYANO 1,3 DIMETHYL 5 (4 HYDROXYPHENYL)1,5 DIHYDROPYRANO[2,3 D]PYRIMIDINE 2,4 DIONE; 7 AMINO 6 CYANO 5 (2,6 DICHLOROPHENYL) 5H PYRANO[2,3 D]PYRIMIDINONE; 7 AMINO 6 CYANO 5 (3 METHOXYLPHENYL) 5H PYRANO[2,3 D]PYRIMIDINE 2,4(1H,3H) DIONE DERIVATIVE; 7 AMINO 6 CYANO 5 (3 METHYLPHENYL) 5H PYRANO[2,3 D]PYRIMIDINE 2,4(1H,3H) DIONE DERIVATIVE; BARBITURIC ACID; METHYL GROUP; PHENOLSULFONPHTHALEIN; PYRANO[2,3 D]PYRIMIDINE DIONE DERIVATIVE; SILICON DIOXIDE; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG; UREASE;

EID: 84874600334     PISSN: 15608115     EISSN: 20082231     Source Type: Journal    
DOI: 10.1186/2008-2231-21-3     Document Type: Article
Times cited : (111)

References (50)
  • 1
    • 0040882240 scopus 로고    scopus 로고
    • In Topics in Current Chemistry
    • Berlin: Springer
    • In Topics in Current Chemistry. Tietze LF, Kettschau G, Volume 189 Berlin: Springer 1997 1 120
    • (1997) Volume 189 , pp. 1-120
    • Tietze, L.F.1    Kettschau, G.2
  • 2
    • 1242289062 scopus 로고
    • Eur. Pat. 163599 (1984)
    • Eur. Pat. 163599 (1984). Kitamura N, Onishi A, Chem Abstr 1984 104 186439
    • (1984) Chem Abstr , vol.104 , pp. 186439
    • Kitamura, N.1    Onishi, A.2
  • 3
    • 0342487061 scopus 로고
    • Pyridopyrimidine derivatives, their production and use. Eur Pat Appl EP 608565 (1994)
    • Pyridopyrimidine derivatives, their production and use. Eur Pat Appl EP 608565 (1994). Furuya S, Ohtaki T, Chem Abstr 1994 121 205395w
    • (1994) Chem Abstr , vol.121
    • Furuya, S.1    Ohtaki, T.2
  • 4
    • 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
    • Positive inotropic activity of 5-amino-6-cyano-1, 3-dimethyl-1, 2, 3, 4-tetrahydropyrido [2, 3-d] pyrim idine-2, 4-dione in cardiac muscle from guinea-pig and man. Part 6: compounds with positive inotropic activity. Heber D, Heers C, Ravens U, Die Pharmazie 1993 48 537 541 7692456 (Pubitemid 23258217)
    • (1993) Pharmazie , vol.48 , Issue.7 , pp. 537-541
    • Heber, D.1    Heers Ravens, C.U.2
  • 5
    • 1242333920 scopus 로고
    • Pyrimidopyrimidine Derivatives. Eur Pat 351058
    • Pyrimidopyrimidine Derivatives. Eur Pat 351058. Coates WJ, Chem Abstr 1990 113 40711
    • (1990) Chem Abstr , vol.113 , pp. 40711
    • Coates, W.J.1
  • 7
    • 0017296451 scopus 로고
    • Pyrido [2,3-d] pyrimidines. IV. Synthetic studies leading to various oxopyrido [2,3-d] pyrimidines
    • 10.1021/jo00869a003 1255289
    • Pyrido [2,3-d] pyrimidines. IV. Synthetic studies leading to various oxopyrido [2,3-d] pyrimidines. Broom AD, Shim JL, Anderson GL, J Org Chem 1976 41 1095 1099 10.1021/jo00869a003 1255289
    • (1976) J Org Chem , vol.41 , pp. 1095-1099
    • Broom, A.D.1    Shim, J.L.2    Anderson, G.L.3
  • 8
    • 0034034944 scopus 로고    scopus 로고
    • An elegant approach towards the regioselective synthesis of deazalumazines through nucleophile induced ring transformation reactions of 6-aryl-3-cyano-4-methylthio-2H-pyran-2-ones
    • An elegant approach towards the regioselective synthesis of deazalumazines through nucleophile induced ring transformation reactions of 6-aryl-3-cyano-4-methylthio-2h-pyran-2-ones. Srivastava P, Saxena AS, Ram VJ, Synthesis 2000 541 544 (Pubitemid 30202208)
    • (2000) Synthesis , Issue.4 , pp. 541-544
    • Srivastava, P.1    Saxena, A.S.2    Ram, V.J.3
  • 9
    • 0000237924 scopus 로고
    • Novel synthesis of pyrido[3,4-d]pyrimidines, pyrido[2,3-d]pyrimidines, and quinazolines via palladium-catalyzed oxidative coupling
    • 10.3987/COM-93-S99
    • Novel synthesis of pyrido[3,4-d]pyrimidines, pyrido[2,3-d]pyrimidines, and quinazolines via palladium-catalyzed oxidative coupling. Hirota K, Kuki H, Maki Y, Heterocycles 1994 37 563 570 10.3987/COM-93-S99
    • (1994) Heterocycles , vol.37 , pp. 563-570
    • Hirota, K.1    Kuki, H.2    Maki, Y.3
  • 10
    • 0141785793 scopus 로고
    • A convenient synthesis of 1,3-diaryl-1,2,3,4,-tetrahydro-5,7,7-trimethyl- 4-oxo-2-thioxo-7H-pyrano[2,3-d ]pyrimidines
    • 10.1016/S0040-4020(01)90530-7
    • A convenient synthesis of 1,3-diaryl-1,2,3,4,-tetrahydro-5,7,7-trimethyl- 4-oxo-2-thioxo-7H-pyrano[2,3-d ]pyrimidines. Ahluwalia VK, Kumar R, Khurana K, Batla R, Tetrahedron 1990 46 3953 3963 10.1016/S0040-4020(01)90530-7
    • (1990) Tetrahedron , vol.46 , pp. 3953-3963
    • Ahluwalia, V.K.1    Kumar, R.2    Khurana, K.3    Batla, R.4
  • 11
    • 0023698375 scopus 로고
    • Reactions of uracils; 15. 7-Ethoxypyrimido[4,5-d]pyrimidines via a uracil-carbodiimide derivative and their products of aminolysis and pyrolysis
    • Reactions of uracils; 15. 7-Ethoxypyrimido[4,5-d]pyrimidines via a uracil-carbodiimide derivative and their products of aminolysis and pyrolysis. Wamhoff H, Muhr J, Synthesis 1988 11 919 921
    • (1988) Synthesis , vol.11 , pp. 919-921
    • Wamhoff, H.1    Muhr, J.2
  • 12
    • 0009264131 scopus 로고
    • A novel one step synthesis of pyrano (2,3-d) pyrimidines
    • 10.1016/S0040-4020(01)87560-8
    • A novel one step synthesis of pyrano (2,3-d) pyrimidines. Ahluvalia VK, Sharma HR, Tyagi R, Tetrahedron 1986 42 4045 4048 10.1016/S0040-4020(01)87560-8
    • (1986) Tetrahedron , vol.42 , pp. 4045-4048
    • Ahluvalia, V.K.1    Sharma, H.R.2    Tyagi, R.3
  • 13
    • 1842552114 scopus 로고
    • Nitrile cyclization reactions. XVI. Reaction of arylidene drivatives of malononitrile and ethyl cyanoacetate with barbituric acid
    • Nitrile cyclization reactions. XVI. Reaction of arylidene drivatives of malononitrile and ethyl cyanoacetate with barbituric acid. Sharanin YA, Klokol GV, Zh Org Khim 1984 20 2448 2452
    • (1984) Zh Org Khim , vol.20 , pp. 2448-2452
    • Sharanin, Y.A.1    Klokol, G.V.2
  • 14
    • 0000154996 scopus 로고
    • Activated nitriles in heterocyclic synthesis: A novel synthesis of pyrano[2,3-d]pyrimidine, pyrano[2,3-c]pyrazole, pyrano[2,3-d]thiazole, and thiazolo[3,2-a]pyridine drivatives
    • Activated nitriles in heterocyclic synthesis: a novel synthesis of pyrano[2,3-d]pyrimidine, pyrano[2,3-c]pyrazole, pyrano[2,3-d]thiazole, and thiazolo[3,2-a]pyridine drivatives. Ibrahim MKA, El-Moghayar MRH, Sharaf MAF, Indian J Chem Sect B 1987 26B 216 219
    • (1987) Indian J Chem Sect B , vol.26 , pp. 216-219
    • Ibrahim, M.K.A.1    El-Moghayar, M.R.H.2    Sharaf, M.A.F.3
  • 15
    • 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
    • Effective synthesis of 7-amino-6-cyano-5-aryl-5H-pyrano[2,3-d]pyrimidine- 2,4(1H,3H)-diones under microwave irradiation. Gao Y, Tu S, Li T, Zhang X, Zhu S, Fang F, Shi D, Synth Commun 2004 34 1295 1299 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
  • 16
    • 19744367285 scopus 로고    scopus 로고
    • A clean one-pot synthesis of 7-amino-5-aryl-6-cyano-1,5-dihydro-2H- pyrano[2,3-d] pyrimidine-2,4(3H)-diones in aqueous media under ultrasonic irradiation
    • Clean one-pot synthesis of 7-amino-5-aryl-6-cyano-1,5-dihydro-2H- pyrano[2,3-d]pyrimidine-2,4(3H)-diones in aqueous media under ultrasonic irradiation. Jin TS, Liu LB, Tu SJ, Zhao Y, Li TS, J Chem Res 2005 3 162 163 (Pubitemid 40744997)
    • (2005) Journal of Chemical Research , Issue.3 , pp. 162-163
    • Jin, T.-S.1    Liu, L.-B.2    Zhao, Y.3    Li, T.-S.4
  • 17
    • 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
    • 10.1007/s11030-008-9079-7 18512127
    • Diammonium hydrogen phosphate as a versatile and efficient catalyst for the one-pot synthesis of pyrano[2,3-d]pyrimidinone derivatives in aqueous media. Balalaie S, Abdolmohammadi S, Bijanzadeh HR, Amani AM, Mol Divers 2008 12 85 91 10.1007/s11030-008-9079-7 18512127
    • (2008) Mol Divers , vol.12 , pp. 85-91
    • Balalaie, S.1    Abdolmohammadi, S.2    Bijanzadeh, H.R.3    Amani, A.M.4
  • 18
    • 77953384477 scopus 로고    scopus 로고
    • Zn[(L)proline]2: An efficient catalyst for the synthesis of biologically active pyrano[2,3-d]pyrimidine derivatives
    • 10.1080/00397910903174390
    • Zn[(L)proline]2: an efficient catalyst for the synthesis of biologically active pyrano[2,3-d]pyrimidine derivatives. Heravi MM, Ghods A, Bakhtiari K, Derikvand F, Synth Commun 2010 40 1927 1931 10.1080/00397910903174390
    • (2010) Synth Commun , vol.40 , pp. 1927-1931
    • Heravi, M.M.1    Ghods, A.2    Bakhtiari, K.3    Derikvand, F.4
  • 20
    • 28844505081 scopus 로고    scopus 로고
    • Green synthesis of pyrano[2,3-d]-pyrimidine derivatives in ionic liquids
    • DOI 10.1080/00397910500282661
    • Green synthesis of pyrano[2,3-d]-pyrimidine derivatives in ionic liquids. Yu J, Wang H, Synth Commun 2005 35 3133 3140 10.1080/00397910500282661 (Pubitemid 41769829)
    • (2005) Synthetic Communications , vol.35 , Issue.24 , pp. 3133-3140
    • Yu, J.1    Wang, H.2
  • 22
    • 77955940284 scopus 로고    scopus 로고
    • H§ssub§14§esub§[NaP§ssub§5§esub§ W§ssub§30§esub§O§ssub§110§esub§] catalyzed one-pot three-component synthesis of dihydropyrano[2,3-c]pyrazole and pyrano[2,3-d]pyrimidine derivatives
    • 10.1007/BF03246049
    • H§ssub§14§esub§[NaP§ssub§5§esub§ W§ssub§30§esub§O§ssub§110§esub§] catalyzed one-pot three-component synthesis of dihydropyrano[2,3-c]pyrazole and pyrano[2,3-d]pyrimidine derivatives. Heravi MM, Ghods A, Derikvand F, Bakhtiari K, Bamoharram FF, J Iran Chem Soc 2010 7 615 620 10.1007/BF03246049
    • (2010) J Iran Chem Soc , vol.7 , pp. 615-620
    • Heravi, M.M.1    Ghods, A.2    Derikvand, F.3    Bakhtiari, K.4    Bamoharram, F.F.5
  • 23
    • 77951221747 scopus 로고    scopus 로고
    • Eco-friendly and efficient synthesis of pyrano[2,3-d] pyrimidinone and tetrahydrobenzo[b]pyran derivatives in water
    • Eco-friendly and efficient synthesis of pyrano[2,3-d] pyrimidinone and tetrahydrobenzo[b]pyran derivatives in water. Mobinikhaledi A, Foroughifar N, Bodaghi Fard MA, Synth React Inorg, Met-Org, Nano-Met Chem 2010 40 179 185
    • (2010) Synth React Inorg, Met-Org, Nano-Met Chem , vol.40 , pp. 179-185
    • Mobinikhaledi, A.1    Foroughifar, N.2    Bodaghi Fard, M.A.3
  • 24
    • 67249089987 scopus 로고    scopus 로고
    • One-pot synthesis of pyrano[2,3-d]pyrimidinone derivatives catalyzed by L-proline in aqueous media
    • 10.1007/BF03245854
    • One-pot synthesis of pyrano[2,3-d]pyrimidinone derivatives catalyzed by L-proline in aqueous media. Bararjanian M, Balalaie S, Movassagh B, Amani AM, J Iran Chem Soc 2009 6 436 442 10.1007/BF03245854
    • (2009) J Iran Chem Soc , vol.6 , pp. 436-442
    • Bararjanian, M.1    Balalaie, S.2    Movassagh, B.3    Amani, A.M.4
  • 25
    • 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
    • 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. Devi I, Kumar BSD, Bhuyan PJ, Tetrahedron Lett 2003 44 8307 8310 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
  • 26
    • 33846970853 scopus 로고    scopus 로고
    • One-pot, three-component condensation reaction in water: An efficient and improved procedure for the synthesis of pyran annulated heterocyclic systems
    • 10.1080/00397910601039242
    • One-pot, three-component condensation reaction in water: an efficient and improved procedure for the synthesis of pyran annulated heterocyclic systems. Shaabani A, Samadi S, Rahmati A, Synth Commun 2007 37 491 499 10.1080/00397910601039242
    • (2007) Synth Commun , vol.37 , pp. 491-499
    • Shaabani, A.1    Samadi, S.2    Rahmati, A.3
  • 27
    • 59349119894 scopus 로고    scopus 로고
    • Mechanochemical solvent-free and catalyst-free one-pot synthesis of pyrano[2,3-d]pyrimidine-2,4(1H,3H)-diones with quantitative yields
    • 10.3390/molecules14010474 19158656
    • Mechanochemical solvent-free and catalyst-free one-pot synthesis of pyrano[2,3-d]pyrimidine-2,4(1H,3H)-diones with quantitative yields. Mashkouri S, Naimi-Jamal MR, Molecules 2009 14 474 479 10.3390/molecules14010474 19158656
    • (2009) Molecules , vol.14 , pp. 474-479
    • Mashkouri, S.1    Naimi-Jamal, M.R.2
  • 28
    • 0026931265 scopus 로고
    • Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism
    • DOI 10.1038/359710a0
    • Ordered mesoporous molecular sieves synthesized by a liquid crystal template mechanism. Kresge CT, Leonowicz ME, Roth WJ, Vartuli JC, Beck JS, Nature 1992 359 710 712 10.1038/359710a0 (Pubitemid 23589384)
    • (1992) Nature , vol.359 , Issue.6397 , pp. 710-712
    • Kresge, C.T.1    Leonowicz, M.E.2    Roth, W.J.3    Vartuli, J.C.4    Beck, J.S.5
  • 29
    • 0029239686 scopus 로고
    • A neutral templating route to mesoporous molecular sieves
    • 10.1126/science.267.5199.865 17813916
    • A neutral templating route to mesoporous molecular sieves. Tanev PT, Pinnavaia TJ, Science 1995 267 865 867 10.1126/science.267.5199.865 17813916
    • (1995) Science , vol.267 , pp. 865-867
    • Tanev, P.T.1    Pinnavaia, T.J.2
  • 30
    • 0345926039 scopus 로고
    • Titanium-containing mesoporous molecular sieves for catalytic oxidation of aromatic compounds
    • DOI 10.1038/368321a0
    • Titanium-containing mesoporous molecular sieves for catalytic oxidation of aromatic compounds. Tanev PT, Chibwe M, Pinnavaia TJ, Nature 1994 368 321 323 10.1038/368321a0 8127366 (Pubitemid 24105637)
    • (1994) Nature , vol.368 , Issue.6469 , pp. 321-323
    • Tanev, P.T.1    Chibwe, M.2    Pinnavaia, T.J.3
  • 31
    • 0040500022 scopus 로고
    • Templating of mesoporous molecular sieves by nonionic polyethylene oxide surfactants
    • Templating of mesoporous molecular sieves by nonionic polyethylene oxide surfactants. Bagshaw SA, Pinnavaia TJ, Science 1995 268 1242 1244
    • (1995) Science , vol.268 , pp. 1242-1244
    • Bagshaw, S.A.1    Pinnavaia, T.J.2
  • 32
    • 0012498083 scopus 로고
    • Liquid-crystalline phases as templates for the synthesis of mesoporous silica
    • 10.1038/378366a0
    • Liquid-crystalline phases as templates for the synthesis of mesoporous silica. Attard GS, Glyde JC, Goliner CG, Nature 1995 378 366 368 10.1038/378366a0
    • (1995) Nature , vol.378 , pp. 366-368
    • Attard, G.S.1    Glyde, J.C.2    Goliner, C.G.3
  • 33
    • 0001627002 scopus 로고
    • Mesostructure design with gemini surfactants: Supercage formation in a three-dimensional hexagonal array
    • 10.1126/science.268.5215.1324 17778977
    • Mesostructure design with gemini surfactants: supercage formation in a three-dimensional hexagonal array. Huo QS, Leon R, Petroff PM, Stucky GD, Science 1995 268 1324 1327 10.1126/science.268.5215.1324 17778977
    • (1995) Science , vol.268 , pp. 1324-1327
    • Huo, Q.S.1    Leon, R.2    Petroff, P.M.3    Stucky, G.D.4
  • 34
    • 0032559316 scopus 로고    scopus 로고
    • Triblock copolymer syntheses of mesoporous silica with periodic 50 to 300 angstrom pores
    • DOI 10.1126/science.279.5350.548
    • Triblock copolymer syntheses of mesoporous silica with periodic 50 to 300 angstrom pores. Zhao DY, Feng JP, Huo QS, Melosh N, Fredrickson GH, Chmelka BF, Stucky GD, Science 1998 279 548 552 10.1126/science.279.5350.548 9438845 (Pubitemid 28067280)
    • (1998) Science , vol.279 , Issue.5350 , pp. 548-552
    • Zhao, D.1    Feng, J.2    Huo, Q.3    Melosh, N.4    Fredrickson, G.H.5    Chmelka, B.F.6    Stucky, G.D.7
  • 35
    • 0031801728 scopus 로고    scopus 로고
    • Nonionic triblock and star diblock copolymer and oligomeric sufactant syntheses of highly ordered, hydrothermally stable, mesoporous silica structures
    • DOI 10.1021/ja974025i
    • Nonionic triblock and star diblock copolymer and oligomeric surfactant syntheses of highly ordered, hydrothermally stable, mesoporous silica structures. Zhao DY, Huo QS, Feng JP, Chmelka BF, Stucky GD, J Am Chem Soc 1998 120 6024 6036 10.1021/ja974025i (Pubitemid 28306987)
    • (1998) Journal of the American Chemical Society , vol.120 , Issue.24 , pp. 6024-6036
    • Zhao, D.1    Huo, Q.2    Feng, J.3    Chmelka, B.F.4    Stucky, G.D.5
  • 36
    • 0033804499 scopus 로고    scopus 로고
    • Morphological control of highly ordered mesoporous silica SBA-15
    • 10.1021/cm9911363
    • Morphological control of highly ordered mesoporous silica SBA-15. Zhao DY, Sun JY, Li QZ, Stucky GD, Chem Mater 2000 12 275 279 10.1021/cm9911363
    • (2000) Chem Mater , vol.12 , pp. 275-279
    • Zhao, D.Y.1    Sun, J.Y.2    Li, Q.Z.3    Stucky, G.D.4
  • 37
    • 0034619913 scopus 로고    scopus 로고
    • Rapid synthesis of mesoporous SBA-15 molecular sieve by a microwave-hydrothermal process
    • Rapid synthesis of mesoporous SBA-15 molecular sieve by a microwave-hydrothermal process. Newalkar BL, Komarneni S, Katsuki H, Chem Commun 2000 23 2389 2390
    • (2000) Chem Commun , vol.23 , pp. 2389-2390
    • Newalkar, B.L.1    Komarneni, S.2    Katsuki, H.3
  • 39
    • 80055013679 scopus 로고    scopus 로고
    • Application of sulfonic acid functionalized nanoporous silica (SBA-Pr-SO§ssub§3§esub§H) for one-pot synthesis of quinoxaline derivatives
    • Application of sulfonic acid functionalized nanoporous silica (SBA-Pr-SO§ssub§3§esub§H) for one-pot synthesis of quinoxaline derivatives. Mohammadi Ziarani G, Badiei A, Haddadpour M, Int J Chem 2011 3 87 94
    • (2011) Int J Chem , vol.3 , pp. 87-94
    • Mohammadi Ziarani, G.1    Badiei, A.2    Haddadpour, M.3
  • 40
    • 78049514370 scopus 로고    scopus 로고
    • One Pot synthesis of polyhydroquinolines catalyzed by sulfonic acid functionalized SBA-15 as a New nanoporous acid catalyst under solvent free conditions
    • One Pot synthesis of polyhydroquinolines catalyzed by sulfonic acid functionalized SBA-15 as a New nanoporous acid catalyst under solvent free conditions. Mohammadi Ziarani G, Badiei A, Khaniania Y, Haddadpour M, Iran J Chem Chem Eng 2010 29 1 10
    • (2010) Iran J Chem Chem Eng , vol.29 , pp. 1-10
    • Mohammadi Ziarani, G.1    Badiei, A.2    Khaniania, Y.3    Haddadpour, M.4
  • 41
    • 84920090794 scopus 로고    scopus 로고
    • Application of sulfonic acid functionalized nanoporous silica (SBA-Pr-SO§ssub§3§esub§H) in the green one-pot synthesis of triazoloquinazolinones and benzimidazoquinazolinones
    • in press 10.1016/j.arabjc.2011.06.020
    • Application of sulfonic acid functionalized nanoporous silica (SBA-Pr-SO§ssub§3§esub§H) in the green one-pot synthesis of triazoloquinazolinones and benzimidazoquinazolinones. Mohammadi Ziarani G, Badiei A, Aslani Z, Lashgari N, Arabian J Chem in press 10.1016/j.arabjc.2011. 06.020
    • Arabian J Chem
    • Mohammadi Ziarani, G.1    Badiei, A.2    Aslani, Z.3    Lashgari, N.4
  • 42
    • 0031801728 scopus 로고    scopus 로고
    • Nonionic triblock and star diblock copolymer and oligomeric sufactant syntheses of highly ordered, hydrothermally stable, mesoporous silica structures
    • DOI 10.1021/ja974025i
    • Nonionic triblock and star diblock copolymer and oligomeric sufactant syntheses of highly ordered, hydrothermally stable, mesoporous silica structures. Zhao DHQ, Feng J, Chmelka BF, Stucky GD, J Am Chem Soc 1998 120 6024 6036 10.1021/ja974025i (Pubitemid 28306987)
    • (1998) Journal of the American Chemical Society , vol.120 , Issue.24 , pp. 6024-6036
    • Zhao, D.1    Huo, Q.2    Feng, J.3    Chmelka, B.F.4    Stucky, G.D.5
  • 43
    • 84874595023 scopus 로고    scopus 로고
    • Application of SBA-Pr-SO§ssub§3§esub§H in the synthesis of benzoxazole derivatives
    • 10.5155/eurjchem.3.4.433-436.673
    • Application of SBA-Pr-SO§ssub§3§esub§H in the synthesis of benzoxazole derivatives. Mohammadi Ziarani G, Badiei A, Shakiba Nahad M, Hassanzadeh M, Eur J Chem 2012 3 433 436 10.5155/eurjchem.3.4.433-436. 673
    • (2012) Eur J Chem , vol.3 , pp. 433-436
    • Mohammadi Ziarani, G.1    Badiei, A.2    Shakiba Nahad, M.3    Hassanzadeh, M.4
  • 44
    • 0033397980 scopus 로고    scopus 로고
    • Python: A programming language for software integration and development
    • Python: a programming language for software integration and development. Sanner MF, J Mol Graph Model 1999 17 57 61 10660911 (Pubitemid 30029318)
    • (1999) Journal of Molecular Graphics and Modelling , vol.17 , Issue.1 , pp. 57-61
    • Sanner, M.F.1
  • 45
    • 70349932423 scopus 로고    scopus 로고
    • AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility
    • 10.1002/jcc.21256 19399780
    • AutoDock4 And AutoDockTools4: automated docking with selective receptor flexibility. Morris GM, Huey R, Lindstrom W, Sanner MF, Belew RK, Goodsell DS, Olson AJ, J Comput Chem 2009 30 2785 2791 10.1002/jcc.21256 19399780
    • (2009) J Comput Chem , vol.30 , pp. 2785-2791
    • Morris, G.M.1    Huey, R.2    Lindstrom, W.3    Sanner, M.F.4    Belew, R.K.5    Goodsell, D.S.6    Olson, A.J.7
  • 46
    • 84864654432 scopus 로고    scopus 로고
    • Large-scale virtual screening for the identification of new helicobacter pylori urease inhibitor scaffolds
    • 10.1007/s00894-011-1310-2 22139480
    • Large-scale virtual screening for the identification of new helicobacter pylori urease inhibitor scaffolds. Azizian H, Nabati F, Sharifi A, Siavoshi F, Mahdavi M, Amanlou M, J Mol Model 2012 18 2917 2927 10.1007/s00894-011-1310-2 22139480
    • (2012) J Mol Model , vol.18 , pp. 2917-2927
    • Azizian, H.1    Nabati, F.2    Sharifi, A.3    Siavoshi, F.4    Mahdavi, M.5    Amanlou, M.6
  • 48
    • 84857543380 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of chalcones of naphtho [2, 1-b] furan condensed with barbituric acid
    • Synthesis and antimicrobial activity of chalcones of naphtho [2, 1-b] furan condensed with barbituric acid. Chandrashekhar C, Latha K, Vagdevi H, Vaidya V, Der Pharma Chemica 2011 3 329 333
    • (2011) Der Pharma Chemica , vol.3 , pp. 329-333
    • Chandrashekhar, C.1    Latha, K.2    Vagdevi, H.3    Vaidya, V.4
  • 49
    • 67651172776 scopus 로고    scopus 로고
    • Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities
    • 10.1016/j.ejmech.2009.05.023 19552984
    • Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities. Yan Q, Cao R, Yi W, Chen Z, Wen H, Ma L, Song H, Eur J Med Chem 2009 44 4235 4243 10.1016/j.ejmech.2009.05.023 19552984
    • (2009) Eur J Med Chem , vol.44 , pp. 4235-4243
    • Yan, Q.1    Cao, R.2    Yi, W.3    Chen, Z.4    Wen, H.5    Ma, L.6    Song, H.7


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