Tailoring flavins for visible light photocatalysis: organocatalytic [2+2] cycloadditions mediated by a flavin derivative and visible light

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F15%3A43900596" target="_blank" >RIV/60461373:22310/15:43900596 - isvavai.cz</a>
Alternative codes found
RIV/60461373:22810/15:43900596
Result on the web
<a href="http://pubs.rsc.org/en/content/articlepdf/2015/cc/c5cc01344e" target="_blank" >http://pubs.rsc.org/en/content/articlepdf/2015/cc/c5cc01344e</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c5cc01344e" target="_blank" >10.1039/c5cc01344e</a>

Result language
angličtina
Original language name
Tailoring flavins for visible light photocatalysis: organocatalytic [2+2] cycloadditions mediated by a flavin derivative and visible light
Original language description
A new application of flavin derivatives in visible light photocatalysis was found. 1-Butyl-7,8-dimethoxy-3-methylalloxazine, when irradiated by visible light, was shown to allow an efficient cyclobutane ring formation via an intramolecular [2+2] cycloaddition of both styrene dienes, considered as electron-rich substrates, and electron-poor bis(arylenones), presumably proceeding via an energy transfer mechanism.
Czech name
—
Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

Project
<a href="/en/project/GA14-09190S" target="_blank" >GA14-09190S: Towards photoorganocatalytic metathesis: [2+2] cycloaddition of alkenes and cyclobutane ring cleavage mediated by flavins and visible light</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2015
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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