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Volumn 69, Issue 3-4, 2011, Pages 333-337

Synthesis of per-substituted hydrophilic and hydrophobic β-cyclodextrin derivatives

Author keywords

Hydrophilic; Hydrophobic; Indium; O perallylated CD; Per 2,3,6 tri O (2 hydroxypent 4 enyl) CD

Indexed keywords


EID: 79955957476     PISSN: 09230750     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10847-010-9749-9     Document Type: Conference Paper
Times cited : (4)

References (14)
  • 3
    • 52649133356 scopus 로고    scopus 로고
    • Influence of water-soluble polymers and surfactants, on mebendazole solubilization by-β-and permethyl-β-cyclodextrins
    • Ba, O.-M., Lahiani-Skiba, M., Joudieh, S., Bounoure, F., Skiba, M.: Influence of water-soluble polymers and surfactants, on mebendazole solubilization by-β-and permethyl-β-cyclodextrins. Drug Gene Deliv. Syst. 2, 386-389 (2008)
    • (2008) Drug Gene Deliv. Syst. , vol.2 , pp. 386-389
    • Ba, O.-M.1    Lahiani-Skiba, M.2    Joudieh, S.3    Bounoure, F.4    Skiba, M.5
  • 4
    • 49049127627 scopus 로고
    • Synthesis of chemically modified cyclodextrins
    • Bartsch, R.-A., Croft, A.-P.: Synthesis of chemically modified cyclodextrins. Tetrahedron 39(9), 1417-1474 (1983)
    • (1983) Tetrahedron. , vol.39 , Issue.9 , pp. 1417-1474
    • Bartsch, R.-A.1    Croft, A.-P.2
  • 5
    • 0001119930 scopus 로고    scopus 로고
    • Methods for selective modifications of cyclodextrins
    • Khan, A., Forgo, P., Stine, K., D'Souza, V.: 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
  • 6
    • 0034657894 scopus 로고    scopus 로고
    • Controlled release of a water-soluble drug, captopril, by a combination of hydrophilic and hydrophobic cyclodextrin derivatives
    • DOI 10.1016/S0168-3659(99)00286-2, PII S0168365999002862
    • Ikeda, Y., Kimura, K., Hirayama, F., Arima, H., Uekama, K.: Controlled release of a water-soluble drug, captopril, by a combination of hydrophilic and hydrophobic cyclodextrin derivatives. J. Control. Release 66 (2-3), 271-280 (2000) (Pubitemid 30160863)
    • (2000) Journal of Controlled Release , vol.66 , Issue.2-3 , pp. 271-280
    • Ikeda, Y.1    Kimura, K.2    Hirayama, F.3    Arima, H.4    Uekama, K.5
  • 7
    • 0035967776 scopus 로고    scopus 로고
    • General approach to the synthesis of persubstituted hydrophilic and amphiphilic β-cyclodextrin derivatives
    • DOI 10.1021/jo010046q
    • Kraus, T., Budesinsky, M., Zavada, J.: General approach to the synthesis of persubstituted hydrophilic and amphiphilic β-cyclodextrin derivatives. J. Org. Chem. 66(13), 4595-4600 (2001) (Pubitemid 32861836)
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.13 , pp. 4595-4600
    • Kraus, T.1    Budesinsky, M.2    Zavada, J.3
  • 8
    • 0037060210 scopus 로고    scopus 로고
    • Improved preparation of perallylated cyclodextrins: Facile synthesis of cyclodextrin-based polycationic and polyanionic compounds
    • DOI 10.1016/S0008-6215(01)00303-2, PII S0008621501003032
    • Ni, J., Singh, S., Wang, L.-X.: Improved preparation of perallylated cyclodextrins: facile synthesis of cyclodextrin-based polycationic and polyanionic compounds. Carbohydr. Res. 337(3), 217-220 (2002) (Pubitemid 34158990)
    • (2002) Carbohydrate Research , vol.337 , Issue.3 , pp. 217-220
    • Ni, J.1    Singh, S.2    Wang, L.-X.3
  • 9
    • 7844226324 scopus 로고    scopus 로고
    • Polyanion inhibitors of HIV and other viruses. 7. Polyanionic compounds and polyzwitterionic compounds derived from cyclodextrins as inhibitors of HIV transmission
    • DOI 10.1021/jm970661f
    • Leydet, A., Moullet, C., Proque, J., Pannecouque, C., Andrei, G., Snoeck, R., Neyts, J., Schols, D., De Clercq, E.: Polyanion inhibitors of HIV and other viruses. 7. Polyanionic compounds and polyzwitterionic compounds derived from cyclodextrins as inhibitors of HIV transmission. J. Med. Chem. 41(25), 4927-4932 (1998) (Pubitemid 28555450)
    • (1998) Journal of Medicinal Chemistry , vol.41 , Issue.25 , pp. 4927-4932
    • Leydet, A.1    Moullet, C.2    Roque, J.P.3    Witvrouw, M.4    Pannecouque, C.5    Andrei, G.6    Snoeck, R.7    Neyts, J.8    Schols, D.9    De Clercq, E.10
  • 10
    • 34547224573 scopus 로고    scopus 로고
    • Per-O-(3-hydroxy)propyl-β-cyclodextrin: A cyclodextrin derivative bearing only primary hydroxyl groups
    • DOI 10.1016/j.carres.2007.06.013, PII S0008621507002844
    • Badi, N., Philippe, Guegan.: Per-O-(3-hydroxy) propyl-β- cyclodextrin: a cyclodextrin derivative bearing only primary hydroxyl groups. Carbohydr. Res. 342, 1989-1991 (2007) (Pubitemid 47126419)
    • (2007) Carbohydrate Research , vol.342 , Issue.14 , pp. 1989-1991
    • Badi, N.1    Guegan, P.2
  • 13
    • 0026045466 scopus 로고
    • Organometailic reactions in aqueous media. Indium-mediated allylation of sulfonimines
    • Li, C.-J., Chan, T.-H.: Organometailic reactions in aqueous media. Indium-mediated allylation of sulfonimines. Tetrahedron Lett. 32, 7017(1991)
    • (1991) Tetrahedron. Lett. , vol.32 , pp. 7017
    • Li, C.-J.1    Chan, T.-H.2
  • 14
    • 1542362215 scopus 로고    scopus 로고
    • Natural (5′-oxoheptene-1′E,3′E-dienyl)-5,6-dihydro-2H- pyran-2-one: Total synthesis and revision of its absolute configuration
    • DOI 10.1016/j.tetlet.2004.01.143, PII S004040390400259X
    • Bouzbouz, S., Lemos, E.-d., Cossy, J., Saez, J., Franck, X., Figadere, B.: Natural (5′-oxoheptene-1′E, 3′ E-dienyl)-5,6-dihydro-2H- pyran-2-one: total synthesis and revision of its absolute configuration. Tetrahedron Lett. 45(12), 2615-2617 (2004) (Pubitemid 38296445)
    • (2004) Tetrahedron Letters , vol.45 , Issue.12 , pp. 2615-2617
    • Bouzbouz, S.1    De Lemos, E.2    Cossy, J.3    Saez, J.4    Franck, X.5    Figadere, B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.