Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F18%3A00101603" target="_blank" >RIV/00216224:14310/18:00101603 - isvavai.cz</a>
Result on the web
<a href="https://pubs.acs.org/doi/10.1021/acsomega.8b00497" target="_blank" >https://pubs.acs.org/doi/10.1021/acsomega.8b00497</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acsomega.8b00497" target="_blank" >10.1021/acsomega.8b00497</a>

Result language
angličtina
Original language name
Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates
Original language 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.
Czech name
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Czech description
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Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
10400 - Chemical sciences

Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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