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
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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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
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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
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