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Volumn 38, Issue 3, 2008, Pages 371-375

High-efficiency conversion of trimethylsilyl ethers to their corresponding ethers using carbon-based solid acid as a new catalyst in heterogeneous mixtures

Author keywords

Carbon based solid acid; Heterogeneous mixtures; Trimethylsilyl ether

Indexed keywords

CARBON; ETHER DERIVATIVE; TRIMETHYLSILYL ETHER DERIVATIVE; UNCLASSIFIED DRUG;

EID: 38649110487     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910701767080     Document Type: Article
Times cited : (4)

References (19)
  • 1
    • 0036736355 scopus 로고    scopus 로고
    • Origins and current status of green chemistry
    • Anastas, P. T.; Kirchhoff, M. M. Origins and current status of green chemistry. Chem. Res. 2002, 35, 686-694.
    • (2002) Chem. Res , vol.35 , pp. 686-694
    • Anastas, P.T.1    Kirchhoff, M.M.2
  • 2
    • 0036736778 scopus 로고    scopus 로고
    • Solid acids for green chemistry
    • Clark, J. H. Solid acids for green chemistry. Chem. Res. 2002, 35, 791-797.
    • (2002) Chem. Res , vol.35 , pp. 791-797
    • Clark, J.H.1
  • 3
    • 0036811256 scopus 로고    scopus 로고
    • Water-tolerant solid acid catalysts
    • Okuhara, T. Water-tolerant solid acid catalysts. Chem. Rev. 2002, 102, 3641-3666.
    • (2002) Chem. Rev , vol.102 , pp. 3641-3666
    • Okuhara, T.1
  • 4
    • 84986834537 scopus 로고
    • Perfluorinated resinsulfonic acid (Nafion-H®) catalysis in synthesis
    • (a) Olah, G. A.; Iyer, P. S.; Prakash, G. K. S. Perfluorinated resinsulfonic acid (Nafion-H®) catalysis in synthesis. Synthesis 1986, 7, 513-531;
    • (1986) Synthesis , vol.7 , pp. 513-531
    • Olah, G.A.1    Iyer, P.S.2    Prakash, G.K.S.3
  • 5
    • 0037149534 scopus 로고    scopus 로고
    • An ordered mesoporous organosilica hybrid material with a crystal-like wall structure
    • (b) Inagaki, S.; Guan, S.; Ohsuna, T.; Terasaki, O. An ordered mesoporous organosilica hybrid material with a crystal-like wall structure. Nature 2002, 416, 304-307.
    • (2002) Nature , vol.416 , pp. 304-307
    • Inagaki, S.1    Guan, S.2    Ohsuna, T.3    Terasaki, O.4
  • 7
    • 0038741672 scopus 로고    scopus 로고
    • Copper(II)-catalyzed ether synthesis from aliphatic alcohols and potassium organotrifluoroborate salts
    • Quach, T. D.; Batey, R. A. Copper(II)-catalyzed ether synthesis from aliphatic alcohols and potassium organotrifluoroborate salts. Org. Lett. 2003, 5, 1381-1384.
    • (2003) Org. Lett , vol.5 , pp. 1381-1384
    • Quach, T.D.1    Batey, R.A.2
  • 8
    • 0037007703 scopus 로고    scopus 로고
    • Buck, E.; Song, Z. J.; Tschaen, D.; Dormer, P. G.; Volante, R. P.; Reider, P. J. Ullmann diaryl ether synthesis: Rate acceleration by 2,2,6,6-tetramethylheptane-3,5-dione. Org. Lett. 2002, 4, 1623-1626.
    • Buck, E.; Song, Z. J.; Tschaen, D.; Dormer, P. G.; Volante, R. P.; Reider, P. J. Ullmann diaryl ether synthesis: Rate acceleration by 2,2,6,6-tetramethylheptane-3,5-dione. Org. Lett. 2002, 4, 1623-1626.
  • 9
    • 0037040317 scopus 로고    scopus 로고
    • Selective etherification of glycerol to polyglycerols over impregnated basic MCM-41 type mesoporous catalysts
    • Clacens, J. M.; Pouilloux, Y.; Barrault, J. Selective etherification of glycerol to polyglycerols over impregnated basic MCM-41 type mesoporous catalysts. Appl. Catal. A-Gen. 2002, 227, 181-190.
    • (2002) Appl. Catal. A-Gen , vol.227 , pp. 181-190
    • Clacens, J.M.1    Pouilloux, Y.2    Barrault, J.3
  • 10
    • 0000463237 scopus 로고    scopus 로고
    • Reductive etherification of substituted cyclohexanones with secondary alcohols catalysed by zeolite H-MCM-22
    • Verhoef, M. J.; Creyghton, E. J.; Peters, J. A. Reductive etherification of substituted cyclohexanones with secondary alcohols catalysed by zeolite H-MCM-22. Chem. Commun. 1997, 20, 1989-1990.
    • (1997) Chem. Commun , vol.20 , pp. 1989-1990
    • Verhoef, M.J.1    Creyghton, E.J.2    Peters, J.A.3
  • 11
    • 0141768458 scopus 로고    scopus 로고
    • The use of Nafion-H® as an efficient catalyst for the direct conversion of primary and secondary trimethylsilyl ethers to their corresponding ethers under mild and heterogeneous conditions
    • Zolfigol, M. A.; Mohammadpoor-Baltork, I.; Habibi, D.; Mirjalili, B. F.; Bamoniria, A. The use of Nafion-H® as an efficient catalyst for the direct conversion of primary and secondary trimethylsilyl ethers to their corresponding ethers under mild and heterogeneous conditions. Tetrahedron Lett. 2003, 44, 8165-8167.
    • (2003) Tetrahedron Lett , vol.44 , pp. 8165-8167
    • Zolfigol, M.A.1    Mohammadpoor-Baltork, I.2    Habibi, D.3    Mirjalili, B.F.4    Bamoniria, A.5
  • 12
    • 0348202833 scopus 로고    scopus 로고
    • Etherification and hydration of isoamylenes with ion exchange resin
    • Linnekoski, J. A.; Krause, A. O. I.; Struckmann, L. K. Etherification and hydration of isoamylenes with ion exchange resin. Appl. Catal. A - Gen. 1998, 170, 117-126.
    • (1998) Appl. Catal. A - Gen , vol.170 , pp. 117-126
    • Linnekoski, J.A.1    Krause, A.O.I.2    Struckmann, L.K.3
  • 13
    • 0035852091 scopus 로고    scopus 로고
    • Interaction between the reaction medium and an ion-exchange resin catalyst in the etherification of iso-amylenes
    • Rihko-Struckmann, L. K.; Latostenmaa, P. V.; Krause, A. O. Interaction between the reaction medium and an ion-exchange resin catalyst in the etherification of iso-amylenes. J. Mol. Catal. A - Chem. 2001, 177, 41-47.
    • (2001) J. Mol. Catal. A - Chem , vol.177 , pp. 41-47
    • Rihko-Struckmann, L.K.1    Latostenmaa, P.V.2    Krause, A.O.3
  • 14
    • 0344241022 scopus 로고    scopus 로고
    • Ion-exchange resin catalysed etherification of dichlopentadiene (DCPD) with methanol
    • Saha, B. Ion-exchange resin catalysed etherification of dichlopentadiene (DCPD) with methanol. React. Funct. Polym. 1999, 40, 51-60.
    • (1999) React. Funct. Polym , vol.40 , pp. 51-60
    • Saha, B.1
  • 15
    • 0042041700 scopus 로고    scopus 로고
    • Novelties of heteropoly acid supported on clay: Etherification of phenethyl alcohol with alkanols
    • Yadav, G. D.; Bokade, V. V. Novelties of heteropoly acid supported on clay: Etherification of phenethyl alcohol with alkanols. Appl. Catal. A - Gen. 1996, 147, 299-323.
    • (1996) Appl. Catal. A - Gen , vol.147 , pp. 299-323
    • Yadav, G.D.1    Bokade, V.V.2
  • 18
    • 33845282062 scopus 로고
    • General ether synthesis under mild acid-free conditions
    • Sassaman, M. B.; Kotian, K. D.; Prakash, G. K. S.; Olah, G. A. General ether synthesis under mild acid-free conditions. J. Org. Chem. 1987, 52, 4314-4319.
    • (1987) J. Org. Chem , vol.52 , pp. 4314-4319
    • Sassaman, M.B.1    Kotian, K.D.2    Prakash, G.K.S.3    Olah, G.A.4
  • 19
    • 0027207477 scopus 로고
    • Zinc chloride catalyzed silylation of alcohols and phenols by examethyldisilazane, A highly chemoselective reaction
    • Firouzabadi, H.; Karimi, B. Zinc chloride catalyzed silylation of alcohols and phenols by examethyldisilazane, A highly chemoselective reaction. Synth. Commun. 1993, 23, 1633.
    • (1993) Synth. Commun , vol.23 , pp. 1633
    • Firouzabadi, H.1    Karimi, B.2


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