Per-2,3-O-alkylated beta-cyclodextrin duplexes connected with disulfide bonds

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F17%3A00474129" target="_blank" >RIV/61388963:_____/17:00474129 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1080/10610278.2016.1164860" target="_blank" >http://dx.doi.org/10.1080/10610278.2016.1164860</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1080/10610278.2016.1164860" target="_blank" >10.1080/10610278.2016.1164860</a>

Result language
angličtina
Original language name
Per-2,3-O-alkylated beta-cyclodextrin duplexes connected with disulfide bonds
Original language description
Per-2,3-di-O-methyl- and per-2,3-di-O-allyl-b-cyclodextrin duplexes held by two disulfide bonds between their primary faces have been prepared. Permethylation significantly increased the solubility of the cyclodextrin duplexes in a wide range of solvents from water to chlorinated hydrocarbons. Per-2,3-di-O-methylated duplexes are able to form inclusion complexes with organic molecules in aqueous solutions, yet the stability constants are lower by 4-5 orders of magnitude as compared to analogous non-alkylated b-cyclodextrin duplexes.
Czech name
—
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
10401 - Organic chemistry

Project
<a href="/en/project/LD12019" target="_blank" >LD12019: Dynamic libraries of cyclodextrin duplexes as a source of high affinity hosts for complexation of organic molecules in aqueous environment.</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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