Bambusurils Bearing Nitro Groups and Their Further Modifications

Investor logo
Investor logo

Warning

This publication doesn't include Faculty of Education. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

YAWER Mirza Arfan SLEZIAKOVÁ Kristína PAVLOVEC Lukáš ŠINDELÁŘ Vladimír

Year of publication 2018
Type Article in Periodical
Magazine / Source European Journal of Organic Chemistry
MU Faculty or unit

Faculty of Science

Citation
Web https://onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201701329
Doi http://dx.doi.org/10.1002/ejoc.201701329
Keywords Macrocycles; Bambusurils; Template synthesis; Receptors; Glycolurils
Description Bambusurils are recently developed neutral anion receptors that show a high affinity towards many inorganic anions, not only in organic solvents but also in water. However, the number of water-soluble bambusurils and also those bearing functional groups is very limited. In this paper we report the synthesis of four- and six-membered bambusurils containing eight and twelve nitro groups. All the nitro groups on the bambusuril portals could be transformed into amino functions, which provided the macrocycles with water solubility and allowed their further modification. For example, we have demonstrated the conversion of amino groups on the bambusurils into the corresponding urea-functionalized bambusuril derivatives. We also report the first example of a bambusuril bearing only two functional groups, which was prepared by the condensation of two different glycolurils.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.