Bambusurils Bearing Nitro Groups and Their Further Modifications
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F18%3A00100977" target="_blank" >RIV/00216224:14310/18:00100977 - isvavai.cz</a>
Alternative codes found
RIV/61389013:_____/18:00485574
Result on the web
<a href="https://onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201701329" target="_blank" >https://onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201701329</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/ejoc.201701329" target="_blank" >10.1002/ejoc.201701329</a>
Alternative languages
Result language
angličtina
Original language name
Bambusurils Bearing Nitro Groups and Their Further Modifications
Original language 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.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10401 - Organic chemistry
Result continuities
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)
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
European Journal of Organic Chemistry
ISSN
1434-193X
e-ISSN
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Volume of the periodical
Neuveden
Issue of the periodical within the volume
1
Country of publishing house
DE - GERMANY
Number of pages
7
Pages from-to
41-47
UT code for WoS article
000419707900005
EID of the result in the Scopus database
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