Bambusuril analogs based on alternating glycoluril and xylylene units

Investor logo
Investor logo

Warning

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

LÍZAL Tomáš ŠINDELÁŘ Vladimír

Year of publication 2019
Type Article in Periodical
Magazine / Source Beilstein journal of organic chemistry
MU Faculty or unit

Faculty of Science

Citation
Web Full Text
Doi http://dx.doi.org/10.3762/bjoc.15.124
Keywords bambusurils; conformers; glycolurils; macrocycles; supramolecular chemistry
Description The glycoluril monomer is a popular building block in supramolecular chemistry as it is used for the synthesis of versatile host molecules which can interact with cationic, anionic or neutral guest molecules. Here we present the design and synthesis of a new hybrid macrocycle containing glycoluril and aromatic units. The reaction afforded a mixture of macrocyclic homologues from which a two-membered macrocycle was isolated as the main product. Two disastereomers of the macrocycle were separated and characterized by means of NMR spectroscopy and X-ray crystallography. Conformational changes of these diastereomers were investigated using DFT models and variable-temperature NMR.
Related projects:

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

More info