Issue 3, 2011
From the journal:

Organic & Biomolecular Chemistry

Asymmetrically substituted calix[4]pyrrole with chiral substituents†

Petr Štěpánek,a   Ondřej Šimák,ab   Zdena Nováková,a   Zdeněk Wimmerc  and  Pavel Drašar*a  

* Corresponding authors

a Institute of Chemical Technology, Prague, Technická 5, Prague 6, Czech Republic
E-mail: Pavel.Drasar@vscht.cz

b Institute of Organic Chemistry and Biochemistry AS CR vvi, Flemingovo nám. 2, Prague 6, Czech Republic

c Institute of Experimental Botany AS CR vvi, Isotope Laboratory, Vídeňská 1083, Prague 4, Czech Republic

Abstract

We have prepared first calix[4]pyrrole containing unprotected carbohydrate moiety directly linked to meso-position of oligopyrrole by stable “C-glycosidic” bond. Basic examination of its superassembly capability is presented.

Graphical abstract: Asymmetrically substituted calix[4]pyrrole with chiral substituents

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Article information

DOI
https://doi.org/10.1039/C0OB00712A
Article type
Communication
Submitted
13 Sep 2010
Accepted
01 Nov 2010
First published
18 Nov 2010

Org. Biomol. Chem., 2011,9, 682-683

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Asymmetrically substituted calix[4]pyrrole with chiral substituents

P. Štěpánek, O. Šimák, Z. Nováková, Z. Wimmer and P. Drašar, Org. Biomol. Chem., 2011, 9, 682 DOI: 10.1039/C0OB00712A

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