Issue 24, 2003
From the journal:

Chemical Communications

A facile synthesis of novel cyclodextrin derivatives incorporating one β-(1,4)-glucosidic bond and their unique inclusion ability†

Toshiyuki Kida,a   Akira Kikuzawa,a   Yohji Nakatsujia  and  Mitsuru Akashi*a  

* Corresponding authors

a Department of Molecular Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan
E-mail: akashi@chem.eng.osaka-u.ac.jp
Fax: +81-6-6879-7359
Tel: +81-6-6879-7356

Abstract

Novel cyclodextrin derivatives incorporating one β-(1,4)-glucosidic bond are easily synthesized in three steps from permethylated α- and β-cyclodextrins, and such host molecules show inclusion selectivity for sodium m-nitrobenzoate over the corresponding p-isomer, in contrast to the cases of the parent permethylated α- and β-cyclodextrins.

Graphical abstract: A facile synthesis of novel cyclodextrin derivatives incorporating one β-(1,4)-glucosidic bond and their unique inclusion ability

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Article information

DOI
https://doi.org/10.1039/B309261E
Article type
Communication
Submitted
06 Aug 2003
Accepted
24 Oct 2003
First published
10 Nov 2003

Chem. Commun., 2003, 3020-3021

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A facile synthesis of novel cyclodextrin derivatives incorporating one β-(1,4)-glucosidic bond and their unique inclusion ability

T. Kida, A. Kikuzawa, Y. Nakatsuji and M. Akashi, Chem. Commun., 2003, 3020 DOI: 10.1039/B309261E

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