메뉴 건너뛰기




Volumn 60, Issue 3-4, 2008, Pages 353-357

Zeolite an efficient catalyst for the Biginelli condensation reaction

Author keywords

Acid sites; Biginelli; Tetrahydropyrimidinones; Zeolite

Indexed keywords


EID: 41549122734     PISSN: 09230750     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10847-007-9384-2     Document Type: Article
Times cited : (36)

References (36)
  • 1
    • 0027205552 scopus 로고
    • 100 years of the Biginelli dihydropyrimidine synthesis
    • A review on DHPMs
    • A review on DHPMs: C.O. Kappe, 100 years of the Biginelli dihydropyrimidine synthesis. Tetrahedron, 49, 6937-6963 (1993)
    • (1993) Tetrahedron , vol.49 , pp. 6937-6963
    • Kappe, C.O.1
  • 2
    • 0037079610 scopus 로고    scopus 로고
    • Multi-component reactions and evolutionary chemistry
    • Weber, L.: Multi-component reactions and evolutionary chemistry. Drug. Discov. Today 7, 143-147 (2002)
    • (2002) Drug. Discov. Today , vol.7 , pp. 143-147
    • Weber, L.1
  • 3
    • 0036603766 scopus 로고    scopus 로고
    • Recent advances in isocyanide-based multicomponent chemistry
    • Domling, A.: Recent advances in isocyanide-based multicomponent chemistry. Curr. Opin. Chem. Biol. 6, 306-313 (2002)
    • (2002) Curr. Opin. Chem. Biol. , vol.6 , pp. 306-313
    • Domling, A.1
  • 4
    • 0034519777 scopus 로고    scopus 로고
    • Biologically active dihydripyrimidones of the Bignelli-type. A literature survey
    • A review, Kappe, C.O. Kappe, Biologically active dihydripyrimidones of the Bignelli-type. A literature survey. Eur. J. Med. Chem., 35, 1043 (2000)
    • (2000) Eur. J. Med. Chem. , vol.35 , pp. 1043
    • Kappe1    Kappe, C.O.2
  • 6
    • 0033615357 scopus 로고    scopus 로고
    • Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen
    • Mayer, T.U., Kapoor, T.M., Haggarty, S.J., King, R.W., Schreiber, S.I., Mitchison, T.J.: Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen. Science 286, 971-974 (1999)
    • (1999) Science , vol.286 , pp. 971-974
    • Mayer, T.U.1    Kapoor, T.M.2    Haggarty, S.J.3    King, R.W.4    Schreiber, S.I.5    Mitchison, T.J.6
  • 8
    • 0026065919 scopus 로고
    • Dihydropyrimidine calcium channel blockers. 3. 3-carbamoyl-4-aryl-1,2,3, 4-tetrahydro-6-methyl-5-pyrimidenecarboxylic acid esters as orally effective antihypertensive agents
    • Atwal, K.S., Swanson, B.N., Unger, S.E., Floyd, D.M., Moreland, S., Hedberg, A., O'Reilly B.C.: Dihydropyrimidine calcium channel blockers. 3. 3-carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidenecarboxylic acid esters as orally effective antihypertensive agents. J. Med. Chem. 34, 806-811 (1991)
    • (1991) J. Med. Chem. , vol.34 , pp. 806-811
    • Atwal, K.S.1    Swanson, B.N.2    Unger, S.E.3    Floyd, D.M.4    Moreland, S.5    Hedberg, A.6    O'Reilly, B.C.7
  • 9
    • 0026759681 scopus 로고
    • Dihydropyrimidine calcium channel blockers. 4, basic 3-substituted-4- aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents
    • Rovinyak, G.C., Atwal, K.S., Hdberg, A., Kimbal, S.D., Moreland, S., Gougoutas, J.Z., O'Reilly, B.C., Schwarts, J., Malley, Malley, M.F.: Dihydropyrimidine calcium channel blockers. 4, basic 3-substituted-4-aryl-1,4- dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents. J. Med. Chem. 35, 3254-3263 (1992)
    • (1992) J. Med. Chem. , vol.35 , pp. 3254-3263
    • Rovinyak, G.C.1    Atwal, K.S.2    Hdberg, A.3    Kimbal, S.D.4    Moreland, S.5    Gougoutas, J.Z.6    O'Reilly, B.C.7    Schwarts, J.8    Malley, M.F.9
  • 10
    • 0006534230 scopus 로고    scopus 로고
    • Design and synthesis of a conformationally rigid mimic of the dihydropyrimidine calcium channel modulator SQ 32,926
    • Kappe, C.O.: Design and synthesis of a conformationally rigid mimic of the dihydropyrimidine calcium channel modulator SQ 32,926. Molecules 5, 227-239 (2000)
    • (2000) Molecules , vol.5 , pp. 227-239
    • Kappe, C.O.1
  • 11
    • 0028939869 scopus 로고
    • Enantioselective total synthesis of (-)-Ptilomycalin A
    • Overman, L.E., Rabinowitz, M.H., Renhowe, P.A.: Enantioselective total synthesis of (-)-Ptilomycalin A. J. Am. Chem. Soc. 117, 2657-2658 (1995)
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 2657-2658
    • Overman, L.E.1    Rabinowitz, M.H.2    Renhowe, P.A.3
  • 12
    • 33751385241 scopus 로고
    • Biomimetic syntheses of Crambines A, B, C1, and C2. Revision of the structures of Crambines B and C1
    • Snider, B.B., Shi, Z.: Biomimetic syntheses of Crambines A, B, C1, and C2. Revision of the structures of Crambines B and C1. J. Org. Chem. 58, 3828 (1993)
    • (1993) J. Org. Chem. , vol.58 , pp. 3828
    • Snider, B.B.1    Shi, Z.2
  • 13
    • 0000176059 scopus 로고
    • Aldehyde-urea derivatives of aceto- and oxaloacetic acids
    • Gazz Biginelli, P.: Aldehyde-urea derivatives of aceto- and oxaloacetic acids. Chim. Itall. 23, 360-413 (1893)
    • (1893) Chim. Itall. , vol.23 , pp. 360-413
    • Gazz Biginelli, P.1
  • 14
    • 34247589261 scopus 로고    scopus 로고
    • A green synthesis of dihydropyrimidinones by Biginelli reaction over Nafion-H catalyst
    • 5
    • Lin, H.X., Zhao, Q.J., Xu, B., Wang, X.H.: A green synthesis of dihydropyrimidinones by Biginelli reaction over Nafion-H catalyst. Chin. Chem. Lett. 18(5), 502-504 (2007)
    • (2007) Chin. Chem. Lett. , vol.18 , pp. 502-504
    • Lin, H.X.1    Zhao, Q.J.2    Xu, B.3    Wang, X.H.4
  • 15
    • 21844436019 scopus 로고    scopus 로고
    • Natural HEU type zeolite catalyzed Biginelli reaction for the synthesis of 3,4-dihydropyrimidin-2(1H) one derivatives
    • 1-2
    • Tajbakhsh, M., Mohajerani, B., Heravi, M.M., Ahmadi, A.N.: Natural HEU type zeolite catalyzed Biginelli reaction for the synthesis of 3,4-dihydropyrimidin-2(1H) one derivatives. J. Mol. Catal. A: Chem. 236(1-2), 216-219 (2005)
    • (2005) J. Mol. Catal. A: Chem. , vol.236 , pp. 216-219
    • Tajbakhsh, M.1    Mohajerani, B.2    Heravi, M.M.3    Ahmadi, A.N.4
  • 16
    • 67049145542 scopus 로고    scopus 로고
    • Zeolite-catalyzed cyclocondensation reaction for the selective synthesis of 3,4-dihydropyrimidin-2(1H)-ones
    • Radha Rani, V., Srinivas, N., Radha Kishan, M., Kulkarni, S.J., Raghavan, K.V.: Zeolite-catalyzed cyclocondensation reaction for the selective synthesis of 3,4-dihydropyrimidin-2(1H)-ones. Green Chem. 3, 305-306 (2001)
    • (2001) Green Chem. , vol.3 , pp. 305-306
    • Radha Rani, V.1    Srinivas, N.2    Radha Kishan, M.3    Kulkarni, S.J.4    Raghavan, K.V.5
  • 18
    • 30944450933 scopus 로고    scopus 로고
    • Convenient one-pot heterogeneous catalytic method for the preparation of 3,4-Dihydropyrimidin-2(1H)-ones
    • 1
    • Adrienn, H., Zoltán, H., Ilona, V.: Convenient one-pot heterogeneous catalytic method for the preparation of 3,4-Dihydropyrimidin-2(1H) -ones. Synth. Commun. 36(1), 129-136 (2006)
    • (2006) Synth. Commun. , vol.36 , pp. 129-136
    • Adrienn, H.1    Zoltán, H.2    Ilona, V.3
  • 19
    • 0142027268 scopus 로고    scopus 로고
    • Efficient synthesis of 3,4-Dihydropyrimidin-2(1 H)-ones over silica sulfuric acid as a reusable catalyst under solvent-free conditions
    • Salehi, P., Dabiri, M., Zolfigol, M.A., Fard, M.A.B.: Efficient synthesis of 3,4-Dihydropyrimidin-2(1 H)-ones over silica sulfuric acid as a reusable catalyst under solvent-free conditions. Heterocycles 60, 2435-2440 (2003)
    • (2003) Heterocycles , vol.60 , pp. 2435-2440
    • Salehi, P.1    Dabiri, M.2    Zolfigol, M.A.3    Fard, M.A.B.4
  • 20
    • 1642353173 scopus 로고    scopus 로고
    • An efficient synthesis of 5-Alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin- 2(1H)-ones catalyzed by KSF montmorillonite
    • Lin, H., Ding, J., Chen, X., Zhang, Z.: An efficient synthesis of 5-Alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones catalyzed by KSF montmorillonite. Molecules 5, 1240-1243 (2000)
    • (2000) Molecules , vol.5 , pp. 1240-1243
    • Lin, H.1    Ding, J.2    Chen, X.3    Zhang, Z.4
  • 23
    • 1642373806 scopus 로고
    • Inorganic solid acids and their use in acid-catalyzed hydrocarbon reactions
    • Corma, A.: Inorganic solid acids and their use in acid-catalyzed hydrocarbon reactions. Chem. Rev. 95, 559 (1995)
    • (1995) Chem. Rev. , vol.95 , pp. 559
    • Corma, A.1
  • 24
    • 0037970270 scopus 로고    scopus 로고
    • Interaction of pesticides with a β-Cyclodextrin derivative studied by reversed-phase thin-layer chromatography and principal component analysis
    • Kooti, M., Zendehdel, M., Mohammadpour Amini, M.: Interaction of pesticides with a β-Cyclodextrin derivative studied by reversed-phase thin-layer chromatography and principal component analysis. J. Incl. Phen. Macrocycl. Chem. 42, 265-268 (2002)
    • (2002) J. Incl. Phen. Macrocycl. Chem. , vol.42 , pp. 265-268
    • Kooti, M.1    Zendehdel, M.2    Mohammadpour Amini, M.3
  • 25
    • 0024619811 scopus 로고
    • Influence of acidity in friedel-crafts acylation catalyzed by zeolites
    • Gauthier, C., Chiche, B., Finiels, A., Genste, P.: Influence of acidity in friedel-crafts acylation catalyzed by zeolites. J. Mol. Catal. 50, 219-229 (1989)
    • (1989) J. Mol. Catal. , vol.50 , pp. 219-229
    • Gauthier, C.1    Chiche, B.2    Finiels, A.3    Genste, P.4
  • 27
    • 17344388928 scopus 로고    scopus 로고
    • 2+ ions into zeolite y using EXAFS techniques
    • 2+ ions into zeolite Y using EXAFS techniques. Solid State Ionic 101, 425-430 (1997)
    • (1997) Solid State Ionic , vol.101 , pp. 425-430
    • Forster, H.1    Hatje, U.2
  • 28
    • 0029292569 scopus 로고
    • The microwave technique: A new route for high dispersion of inorganic salts onto supports
    • Xiao, F.S., Wu, W., Qiu, S., Xu, R.: The microwave technique: a new route for high dispersion of inorganic salts onto supports. J. Mat. Sci. Lett. 14, 598-599 (1993)
    • (1993) J. Mat. Sci. Lett. , vol.14 , pp. 598-599
    • Xiao, F.S.1    Wu, W.2    Qiu, S.3    Xu, R.4
  • 33
    • 34248206904 scopus 로고
    • Assigned to union carbide
    • Pat. No.3130007, patented, April 21
    • Breck, D.W., Tonawanda, N.Y.: Assigned to union carbide, Pat. No.3130007, patented, April 21, 1964
    • (1964)
    • Breck, D.W.1    Tonawanda, N.Y.2
  • 34
    • 22544473660 scopus 로고    scopus 로고
    • 2O onto the surface of NaY zeolite using microwave irradiation
    • 2O onto the surface of NaY zeolite using microwave irradiation. J Pores Mater. 12, 143-149 (2005)
    • (2005) J Pores Mater. , vol.12 , pp. 143-149
    • Zendehdel, M.1    Kooti, M.2    Amini, M.M.3
  • 35
    • 37049086952 scopus 로고
    • Acidity of aluminophosphate structures. Part 2.-Incorporation of cobalt into CHA and AFI by microwave synthesis
    • Lohose, U., Bertran, R., Jancke, K., Kurzawski, L., Parlitz, B., Lofler, E., Schreier, E: Acidity of aluminophosphate structures. Part 2.-Incorporation of cobalt into CHA and AFI by microwave synthesis. J.Chem.Soc. Faraday Trans. 91, 1163-1172 (1995)
    • (1995) J.Chem.Soc. Faraday Trans. , vol.91 , pp. 1163-1172
    • Lohose, U.1    Bertran, R.2    Jancke, K.3    Kurzawski, L.4    Parlitz, B.5    Lofler, E.6    Schreier, E.7
  • 36
    • 1042263383 scopus 로고    scopus 로고
    • 2 supported on NaY zeolite by solid-state interaction under microwave irradiation and used as heterogeneous catalysts for high regioselective Diels-Alder reaction of myrcene and acrolein
    • 2 supported on NaY zeolite by solid-state interaction under microwave irradiation and used as heterogeneous catalysts for high regioselective Diels-Alder reaction of myrcene and acrolein. J. Mol Catal A, Chem. 209, 171-177 (2004)
    • (2004) J. Mol Catal A, Chem. , vol.209 , pp. 171-177
    • Liu, J.1    Yin, D.2    Yin, D.3    Fu, Z.4    Li, Q.5    Lu, G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.