Perhaloalkylation of Metal Enolates?Unconventional and Versatile

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F11%3A00361368" target="_blank" >RIV/61388963:_____/11:00361368 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1002/anie.201007672" target="_blank" >http://dx.doi.org/10.1002/anie.201007672</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/anie.201007672" target="_blank" >10.1002/anie.201007672</a>

Result language
angličtina
Original language name
Perhaloalkylation of Metal Enolates?Unconventional and Versatile
Original language description
Radically unconventional: Natural products with di- and trichloromethyl groups and trifluoromethylated pharmaceuticals and agrochemicials are interesting compounds, often with intriguing properties. These types of compounds can be prepared by the directperhaloalkylation of carbonyl compounds in which enolate reactivity and radical reactivity are merged.
Czech name
—
Czech description
—

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/GA203%2F09%2F1936" target="_blank" >GA203/09/1936: Unprecedented Domino Processes Involving the Directed Application of Anionic, Transition Metal-Catalyzed, Radical and Carbocationic Reaction Steps</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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