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Cyclodextrin hydroxyalkyl

Poly(benzimidazole) can be used as the reactive polymer for the preparation of side chain-type polyrotaxane via the alkylation on nitrogen. Osakada et al. showed that deprotonation of poly(benzimidazole) followed by N-alkylation with alkyl bromide-terminated pseudorotaxane consisting of 2,3,6-trimethyl-/1-cyclodextrin gave a novel side chain-type polyrotaxane (Scheme 38) [206]. Poly(benzimidazole) having a long -hydroxyalkyl group as the side chain can form an inclusion complex with 2,3,6-trimethyl-/l-cy-... [Pg.44]

A Yoshida, H Arima, K Uekama, J Pitha. Pharmaceutical evaluation of hydroxyalkyl ethers of -cyclodextrins. Int J Pharm 46 217-222, 1988. [Pg.203]


See other pages where Cyclodextrin hydroxyalkyl is mentioned: [Pg.159]    [Pg.840]    [Pg.181]    [Pg.27]    [Pg.695]    [Pg.587]    [Pg.159]    [Pg.827]    [Pg.669]    [Pg.85]    [Pg.381]    [Pg.836]    [Pg.13]    [Pg.91]    [Pg.608]   
See also in sourсe #XX -- [ Pg.845 ]




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Hydroxyalkyl

Hydroxyalkylation

Hydroxyalkylations

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