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Syntheses of fluorooxindole and 2-fluoro-2-arylacetic acid derivatives from diethyl 2-fluoromalonate ester
- Source :
- Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1213-1219 (2014), Beilstein journal of organic chemistry, 2014, Vol.10, pp.1213-1219 [Peer Reviewed Journal], Beilstein Journal of Organic Chemistry
- Publication Year :
- 2014
- Publisher :
- Beilstein-Institut, 2014.
-
Abstract
- Diethyl 2-fluoromalonate ester is utilised as a building block for the synthesis of 2-fluoro-2-arylacetic acid and fluorooxindole derivatives by a strategy involving nucleophilic aromatic substitution reactions with ortho-fluoronitrobenzene substrates followed by decarboxylation, esterification and reductive cyclisation processes.
- Subjects :
- organo-fluorine
Chemistry
Decarboxylation
Organic Chemistry
fluoroarylacetic acid
Fluoroarylacetic acid
Fluorooxindole
fluorinated building blocks
fluoromalonate
Fluorinated building blocks
Selective fluorination
Full Research Paper
lcsh:QD241-441
Fluoromalonate
Organo-fluorine
fluorooxindole
lcsh:Organic chemistry
Nucleophilic aromatic substitution
Block (telecommunications)
Organic chemistry
selective fluorination
lcsh:Q
lcsh:Science
Subjects
Details
- Language :
- English
- ISSN :
- 18605397
- Volume :
- 10
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Beilstein Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....c5413e198322938993ab57b2a7dbecec