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Volumn 69, Issue 3-4, 2011, Pages 425-431

Regioselective difunctionalization of cyclodextrins

Author keywords

Artificial enzymes; Catalysis; Cyclodextrins; Difunctionalization; Supramolecular

Indexed keywords


EID: 79955967931     PISSN: 09230750     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10847-010-9775-7     Document Type: Conference Paper
Times cited : (6)

References (31)
  • 1
    • 0001354595 scopus 로고    scopus 로고
    • Industrial applications of cyclodextrins
    • Hedges, A. R.: Industrial applications of cyclodextrins. Chem. Rev. 98, 2035-2044 (1998) (Pubitemid 128633446)
    • (1998) Chemical Reviews , vol.98 , Issue.5 , pp. 2035-2044
    • Hedges, A.R.1
  • 2
    • 0032119526 scopus 로고    scopus 로고
    • Cyclodextrin drug carrier system
    • Uekama, K., Hirayama, F., Irie, T.: Cyclodextrin drug carrier system. Chem. Rev. 98, 2045-2076 (1998)
    • (1998) Chem. Rev. , vol.98 , pp. 2045-2076
    • Uekama, K.1    Hirayama, F.2    Irie, T.3
  • 3
    • 1842582944 scopus 로고    scopus 로고
    • Biomimetic reactions catalyzed by cyclodextrins and their derivatives
    • Breslow, R., Dong, S. D.: Biomimetic reactions catalyzed by cyclodextrins and their derivatives. Chem. Rev. 98, 1997-2011 (1998) (Pubitemid 128633444)
    • (1998) Chemical Reviews , vol.98 , Issue.5 , pp. 1997-2011
    • Breslow, R.1    Dong, S.D.2
  • 6
    • 4243778369 scopus 로고    scopus 로고
    • Complexation thermodynamics of cyclodextrins
    • Rekharsky, M. V., Inoue, Y.: Complexation thermodynamics of cyclodextrins. Chem. Rev. 98, 1875-1917 (1998) (Pubitemid 128633440)
    • (1998) Chemical Reviews , vol.98 , Issue.5 , pp. 1875-1917
    • Rekharsky, M.V.1    Inoue, Y.2
  • 7
    • 0001119930 scopus 로고    scopus 로고
    • Methods for selective modifications of cyclodextrins
    • Khan, A. R., Forgo, P., Stine, K. J., D'Souza, V. T.: Methods for selective modifications of cyclodextrins. Chem. Rev. 98, 1977-1996 (1998) (Pubitemid 128633443)
    • (1998) Chemical Reviews , vol.98 , Issue.5 , pp. 1977-1996
    • Khan, A.R.1    Forgo, P.2    Stine, K.J.3    D'Souza, V.T.4
  • 8
    • 0000227522 scopus 로고
    • The highly selective sulfonylation of cycloheptaamylose and syntheses of its pure amino derivatives
    • references herein
    • Tsujihara, K., Kurita, H., Kawazu, M.: The highly selective sulfonylation of cycloheptaamylose and syntheses of its pure amino derivatives. Bull. Chem. Soc. Jpn. 50, 1567-1571 (1977) and references herein
    • (1977) Bull. Chem. Soc. Jpn. , vol.50 , pp. 1567-1571
    • Tsujihara, K.1    Kurita, H.2    Kawazu, M.3
  • 10
    • 0035809374 scopus 로고    scopus 로고
    • Diisobutylaluminium-promoted regioselective de-O-methylation of cyclodextrins: An expeditious entry to selectively modified cyclodextrins
    • DOI 10.1016/S0957-4166(01)00065-9, PII S0957416601000659
    • Wang, W., Pearce, A. J., Zhang, Y., Sinaÿ, P.: Diisobutylaluminium- promotedregioselective de-O-methylation of cyclodextrins: an expeditious entry toselectively modified cyclodextrins. Tetrahedron Asymmetr. 12, 517-523 (2001) (Pubitemid 32299929)
    • (2001) Tetrahedron Asymmetry , vol.12 , Issue.3 , pp. 517-523
    • Wang, W.1    Pearce, A.J.2    Zhang, Y.3    Sinay, P.4
  • 11
    • 41649104155 scopus 로고    scopus 로고
    • Multiple homo- and hetero-functionalizations of α-cyclodextrin through oriented deprotections
    • DOI 10.1021/jo7027085
    • Guieu, S., Sollogoub, M.: Multiple homo-and hetero-functionalizations of "-cyclodextrin through oriented deprotections". J. Org. Chem. 73, 2819-2828 (2008) (Pubitemid 351482994)
    • (2008) Journal of Organic Chemistry , vol.73 , Issue.7 , pp. 2819-2828
    • Guieu, S.1    Sollogoub, M.2
  • 12
    • 37249086730 scopus 로고    scopus 로고
    • Chemical clockwise tridifferentiation of α- and β-cyclodextrins: Bascule-bridge or deoxy-sugars strategies
    • DOI 10.1002/chem.200700971
    • Bistri, O., Sinaÿ, P., Barbero, J. J., Sollogoub, M.: CChemical clockwise tridifferentiation of α-and β-cyclodextrins: basculebridge or deoxy-sugars strategies. Chem. Eur. J. 13, 9757-9774 (2007) (Pubitemid 350279688)
    • (2007) Chemistry - A European Journal , vol.13 , Issue.35 , pp. 9757-9774
    • Bistri, O.1    Sinay, P.2    Barbero, J.J.3    Sollogoub, M.4
  • 13
    • 7044274395 scopus 로고    scopus 로고
    • An artificial enzyme that catalyzes hydrolysis of aryl glycosides
    • DOI 10.1016/j.tetlet.2004.09.134, PII S004040390402115X
    • Rousseau, C., Nielsen, N., Bols, M.: An artificial enzyme that catalyzes hydrolysis of aryl glycosides. Tetrahedron Lett. 45, 8709-8711 (2004) (Pubitemid 39421479)
    • (2004) Tetrahedron Letters , vol.45 , Issue.47 , pp. 8709-8711
    • Rousseau, C.1    Nielsen, N.2    Bols, M.3
  • 16
    • 24144503694 scopus 로고    scopus 로고
    • Four orders of magnitude rate increase in artificial enzyme-catalyzed aryl glycoside hydrolysis
    • DOI 10.1021/jo050861w
    • Ortega-Caballero, F., Bjerre, J., Laustsen, L. S., Bols, M.: Four orders of magnitude rate increase in artificial enzyme-catalyzed aryl glycoside hydrolysis. J. Org. Chem. 70, 7217-7226 (2005) (Pubitemid 41233258)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.18 , pp. 7217-7226
    • Ortega-Caballero, F.1    Bjerre, J.2    Laustsen, L.S.3    Bols, M.4
  • 17
    • 29344463392 scopus 로고    scopus 로고
    • Supramolecular oxidation of anilines using hydrogen peroxide as stoichiometric oxidant
    • DOI 10.1021/ja054457q
    • Marinescu, L., Mølbach, M., Rousseau, C., Bols, M.: Supramolecular oxidation of anilines using hydrogen peroxide as stoichiometric oxidant. J. Am. Chem. Soc. 127, 17578-17579 (2005) (Pubitemid 43003353)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.50 , pp. 17578-17579
    • Marinescu, L.1    Molbach, M.2    Rousseau, C.3    Bols, M.4
  • 18
    • 33746281446 scopus 로고    scopus 로고
    • Very high rate enhancement of benzyl alcohol oxidation by an artificial enzyme
    • DOI 10.1002/anie.200600812
    • Marinescu, L., Bols, M.: Very high rate enhancement of benzyl alcohol oxidation by an artificial enzyme. Angew. Chem. Int. Ed. 45, 4590-4593 (2006) (Pubitemid 44106072)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.28 , pp. 4590-4593
    • Marinescu, L.G.1    Bols, M.2
  • 19
    • 34447642539 scopus 로고    scopus 로고
    • New cup-shaped α-cyclodextrin derivatives and a study of their catalytic properties in oxidation reactions
    • DOI 10.1016/j.tet.2007.06.018, PII S0040402007010459
    • Lopez, O. L., Marinescu, L., Bols, M.: New cup-shaped-cyclodextrin derivatives and a study of their catalytic properties in oxidation reactions. Tetrahedron 63, 8872-8880 (2007) (Pubitemid 47087863)
    • (2007) Tetrahedron , vol.63 , Issue.36 , pp. 8872-8880
    • Lopez, O.L.1    Marinescu, L.2    Bols, M.3
  • 20
    • 33846644499 scopus 로고    scopus 로고
    • Synthesis of some trifluoromethylated cyclodextrin derivatives and analysis of their properties as artificial glycosidases and oxidases
    • Bjerre, J., Fenger, T. H., Marinescu, L., Bols, M.: Synthesis of some trifluoromethylated cyclodextrin derivatives and analysis of their properties as artificial glycosidases and oxidases. Eur. J. Org. Chem. 4, 704-710 (2007)
    • (2007) Eur. J. Org. Chem. , vol.4 , pp. 704-710
    • Bjerre, J.1    Fenger, T.H.2    Marinescu, L.3    Bols, M.4
  • 21
    • 60749098409 scopus 로고    scopus 로고
    • Cyclodextrin ketones as oxidation catalysts: Investigation of bridged derivatives
    • Fenger, T. H., Marinescu, L., Bols, M.: Cyclodextrin ketones as oxidation catalysts: investigation of bridged derivatives. Org. Biomol. Chem. 7, 933-943 (2009)
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 933-943
    • Fenger, T.H.1    Marinescu, L.2    Bols, M.3
  • 23
    • 33745892930 scopus 로고    scopus 로고
    • Cyclodextrin derivatives with cyanohydrin and carboxylate groups as artificial glycosidases
    • DOI 10.1139/V06-039
    • Ortega-Caballero, F., Bols, M.: Cyclodextrin derivatives with cyanohydrin and carboxylate groups as artificial glycosidases. Can. J. Chem. 84, 650-658 (2006) (Pubitemid 44047315)
    • (2006) Canadian Journal of Chemistry , vol.84 , Issue.4 , pp. 650-658
    • Ortega-Caballero, F.1    Bols, M.2
  • 24
    • 35748940325 scopus 로고    scopus 로고
    • A hydrophilic cyclodextrin duplex forming supramolecular assemblies by physical cross-linking of a biopolymer
    • DOI 10.1002/chem.200700800
    • Bistri, O., Mazeau, K., Auzely-Velty, R., Sollogoub, M.: A hydrophilic cyclodextrin duplex forming supramolecular assemblies by physical cross-linking of a biopolymer. Chem. Eur. J. 13, 8847-8857 (2007) (Pubitemid 350044770)
    • (2007) Chemistry - A European Journal , vol.13 , Issue.31 , pp. 8847-8857
    • Bistri, O.1    Mazeau, K.2    Auzely-Velty, R.3    Sollogoub, M.4
  • 25
    • 54749083765 scopus 로고    scopus 로고
    • Regiospecific tandem azide-reduction/deprotection to afford versatile amino alcohol-functionalized-and-cyclodextrins
    • Guieu, S., Sollogoub, M.: Regiospecific tandem azide-reduction/ deprotection to afford versatile amino alcohol-functionalized-and-cyclodextrins. Angew. Chem. Int. Ed. 47, 7060-7063 (2008)
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 7060-7063
    • Guieu, S.1    Sollogoub, M.2
  • 26
    • 65549149571 scopus 로고    scopus 로고
    • Selective discrimination of cyclodextrin diols using cyclic sulfates
    • Petrillo, M., Marinescu, L., Rousseau, C., Bols, M.: Selective discrimination of cyclodextrin diols using cyclic sulfates. Org. Lett. 11, 1983-1985 (2009)
    • (2009) Org. Lett. , vol.11 , pp. 1983-1985
    • Petrillo, M.1    Marinescu, L.2    Rousseau, C.3    Bols, M.4
  • 27
    • 70350524980 scopus 로고    scopus 로고
    • Cyclodextrin aldehydes are oxidase mimics
    • Fenger, T. H., Bjerre, J., Bols, M.: Cyclodextrin aldehydes are oxidase mimics. Chem. Biol. Chem. 10, 2494-2503 (2009)
    • (2009) Chem. Biol. Chem. , vol.10 , pp. 2494-2503
    • Fenger, T.H.1    Bjerre, J.2    Bols, M.3
  • 28
    • 0002922211 scopus 로고
    • Organotin derivatives and the selective acylation and alkylation of the equatorial hydroxy group in a vicinal, equatorial-axial pair
    • Nashed, M. A., Anderson, L.: Organotin derivatives and the selective acylation and alkylation of the equatorial hydroxy group in a vicinal, equatorial-axial pair. Tetrahedron Lett. 11, 3503-3506 (1976)
    • (1976) Tetrahedron. Lett. , vol.11 , pp. 3503-3506
    • Nashed, M.A.1    Anderson, L.2
  • 29
    • 0010233142 scopus 로고
    • Synthetic oligosaccharides related to group B streptococcal polysaccharides. 5. Combined chemical and enzymic synthesis of a pentasaccharide repeating unit of the capsular polysaccharide of type III group B Streptococcus and one-and two-dimensional NMR spectroscopic studies
    • Poszgay, V., Brisson, J.-R., Jennings, H. J., Allen, S., Paulson, J. C.: Synthetic oligosaccharides related to group B streptococcal polysaccharides. 5. Combined chemical and enzymic synthesis of a pentasaccharide repeating unit of the capsular polysaccharide of type III group B Streptococcus and one-and two-dimensional NMR spectroscopic studies. J. Org. Chem. 56, 3377-3385 (1991)
    • (1991) J. Org. Chem. , vol.56 , pp. 3377-3385
    • Poszgay, V.1    Brisson, J.-R.2    Jennings, H.J.3    Allen, S.4    Paulson, J.C.5
  • 30
    • 37049106842 scopus 로고
    • Regioselective reductive ring opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protective group strategy
    • Johansson, R., Samuelsson, B.: Regioselective reductive ring opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protective group strategy. J. Chem. Soc., Chem. Commun. 3, 201-202 (1984)
    • (1984) J. Chem. Soc., Chem. Commun. , vol.3 , pp. 201-202
    • Johansson, R.1    Samuelsson, B.2
  • 31
    • 41349108061 scopus 로고    scopus 로고
    • Synthesis of aminocyclodextrin carboxylic acids
    • DOI 10.1055/s-2008-1042803
    • Hanessian, S., Hocquelet, C., Jankowski, C. K.: Synthesis of aminocyclodextrin carboxylic acids. Synlett 5, 715-719 (2008) (Pubitemid 351449006)
    • (2008) Synlett , Issue.5 , pp. 715-719
    • Hanessian, S.1    Hocquelet, C.2    Jankowski, C.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.