Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates
| Authors | |
|---|---|
| Year of publication | 2018 |
| Type | Article in Periodical |
| Magazine / Source | ACS Omega |
| MU Faculty or unit | |
| 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. |
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