Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates

Investor logo
Investor logo

Warning

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

HAVEL Václav SADILOVÁ Tereza ŠINDELÁŘ Vladimír

Year of publication 2018
Type Article in Periodical
Magazine / Source ACS Omega
MU Faculty or unit

Faculty of Science

Citation
Web https://pubs.acs.org/doi/10.1021/acsomega.8b00497
Doi http://dx.doi.org/10.1021/acsomega.8b00497
Keywords INHIBITORS; BINDING; ANIONS
Description A new bambusuril derivative, (H)BU[6], lacking substituents on the ureidic nitrogen atoms, has been isolated and characterized. This macrocycle was prepared by the deprotection of bambusuril (PMB)BU[6]. (H)BU[6] is attractive for use as a starting compound for the preparation of other bambusuril derivatives, which was demonstrated via propargylation and the copper-catalyzed click reaction performed on the macrocycle.
Related projects:

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

More info