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Synthesis of substituted cyclodextrins

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F46747885%3A24620%2F19%3A00005916" target="_blank" >RIV/46747885:24620/19:00005916 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s10311-018-0779-7" target="_blank" >http://dx.doi.org/10.1007/s10311-018-0779-7</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s10311-018-0779-7" target="_blank" >10.1007/s10311-018-0779-7</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis of substituted cyclodextrins

  • Original language description

    Cyclodextrins are naturally occurring, non-toxic and biodegradable cyclic oligosaccharides. The main feature of cyclodextrins is the ability to encapsulate lipophilic compounds, which has led to many applications. Although many cyclodextrin derivatives have become available on the market, their price is in the range of fine chemicals, and thus, they are still often synthesised in laboratories. The actual number of cyclodextrin derivatives exceeds 11,000, but new cyclodextrin derivatives are still needed for more advanced applications. Therefore, many beginners in cyclodextrin chemistry struggle with a reliable choice of a synthetic route. This review focuses on cyclodextrin derivatives that can be subsequently modified. Indeed, the modification of an already substituted cyclodextrin with a suitable functional group is much easier than the optimisation of the substitution for every new cyclodextrin derivative desired. This review describes the synthesis of different types of cyclodextrin derivatives: persubstituted, randomly substituted, persubstituted at selected positions, selectively substituted and monosubstituted cyclodextrins.

  • Czech name

  • Czech description

Classification

  • 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

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

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Environmental Chemistry Letters

  • ISSN

    1610-3653

  • e-ISSN

  • Volume of the periodical

    17

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    15

  • Pages from-to

    49-63

  • UT code for WoS article

    000463141100003

  • EID of the result in the Scopus database

    2-s2.0-85050156885