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Insight into the catalytic activity of alloxazinium and isoalloxazinium salts in the oxidations of sulfides and amines with hydrogen peroxide

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F12%3A43893696" target="_blank" >RIV/60461373:22310/12:43893696 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.molcata.2012.07.012" target="_blank" >http://dx.doi.org/10.1016/j.molcata.2012.07.012</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.molcata.2012.07.012" target="_blank" >10.1016/j.molcata.2012.07.012</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Insight into the catalytic activity of alloxazinium and isoalloxazinium salts in the oxidations of sulfides and amines with hydrogen peroxide

  • Original language description

    In addition to the already known organocatalysts dihydro-5-ethylalloxazines 1-H2 and 5-ethylisoalloxazinium salts 2, other derivatives of alloxazines and isoalloxazines (flavins) have been shown to catalyze the oxidation of sulfides to sulfoxides with hydrogen peroxide with high efficiency. In the alloxazine series, the C4a-methoxy adduct 1-OCH3 or 5-ethylalloxazinium salts 1 can also be used, but the latter only in the presence of a base, as a co-catalyst. In the isoalloxazine series, the C4a-hydroxy adduct 2-OH or dihydroform 2-H2 can also be utilized but only in the presence of the catalytic amount of an acid. On the other hand, only alloxazine derivatives, i.e. dihydroalloxazines 1-H2 and their methoxy adducts 1-OCH3 or alloxazinium salts 1 can beused as catalysts for the oxidation of tertiary amines, as the catalytic activity of isoalloxazinium salts 1 and their derivatives is inhibited under basic conditions. The different reactivity of the alloxazinium and isoalloxazinium catal

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GAP207%2F12%2F0447" target="_blank" >GAP207/12/0447: Organocatalytic stereoselective oxidations using heterocyclic hydroperoxides</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2012

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal Of Molecular Catalysis A-Chemical

  • ISSN

    1381-1169

  • e-ISSN

  • Volume of the periodical

    363

  • Issue of the periodical within the volume

    Neuveden

  • Country of publishing house

    BE - BELGIUM

  • Number of pages

    9

  • Pages from-to

    362-370

  • UT code for WoS article

    000309443400047

  • EID of the result in the Scopus database