Issue 9, 2002
From the journal:

Chemical Communications

The formation of a cyclic diacetal of methyl α-D-mannopyranoside with a 16-membered macrocyclic loop

Jolanta Maslinska-Solich,*a   Nikodem Kuznik,b   Maciej Kubickic  and  Sylwia Kukowkaa  

* Corresponding authors

a Institute of Physico-Chemistry and Polymer Technology, Silesian University of Technology, Strzody 9, Gliwice, Poland
E-mail: jms1acet@zeus.polsl.gliwice.pl

b Institute of Inorganic Chemistry, Technology and Electrochemistry, Silesian University of Technology, Krzywoustego 6, Gliwice, Poland
E-mail: nikodem@zeus.polsl.gliwice.pl

c Faculty of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, Poznan, Poland

Abstract

The X-ray structure of a diacetal with a 16-membered macrocyclic loop, which was obtained as a product of the condensation of methyl α-D-mannopyranoside and 1,4-bis(2-formylphenoxy)butane is presented together with polymeric compounds resulting from polycondensation; a similar polymer was formed in the reaction of methyl 2,3:4,6-di-O-salicylidene-α-D-mannopyranoside with 1,4-dibromobutane.

Graphical abstract: The formation of a cyclic diacetal of methyl α-D-mannopyranoside with a 16-membered macrocyclic loop

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Article information

DOI
https://doi.org/10.1039/B202273G
Article type
Communication
Submitted
04 Mar 2002
Accepted
21 Mar 2002
First published
05 Apr 2002

Chem. Commun., 2002, 984-985

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The formation of a cyclic diacetal of methyl α-D-mannopyranoside with a 16-membered macrocyclic loop

J. Maslinska-Solich, N. Kuznik, M. Kubicki and S. Kukowka, Chem. Commun., 2002, 984 DOI: 10.1039/B202273G

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