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Chemistry of detrifluoroacetylativelyin situgenerated fluoro-enolates
- Source :
- Organic & Biomolecular Chemistry. 17:762-775
- Publication Year :
- 2019
- Publisher :
- Royal Society of Chemistry (RSC), 2019.
-
Abstract
- This review article comprehensively profiles all literature reports (2015-2018) related to the detrifluoroacetylative in situ generation of fluorine-containing enolates and their reactions with electrophilic reagents. The innovative facets of this unconventional methodology and its synthetic generality for the preparation of fluorine-containing compounds of high medicinal value are highlighted.
- Subjects :
- In situ
010405 organic chemistry
Chemistry
Organic Chemistry
010402 general chemistry
floroorganic compound
01 natural sciences
Biochemistry
Combinatorial chemistry
alfa-fluoroenolates
0104 chemical sciences
Electrophile
Detrifluoroacetylation
Physical and Theoretical Chemistry
Value (mathematics)
Detrifluoroacetylation, floroorganic compound, alfa-fluoroenolates
Subjects
Details
- ISSN :
- 14770539 and 14770520
- Volume :
- 17
- Database :
- OpenAIRE
- Journal :
- Organic & Biomolecular Chemistry
- Accession number :
- edsair.doi.dedup.....273490e3acca1e5823639d29da51dc4f
- Full Text :
- https://doi.org/10.1039/c8ob02843e