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Formation of Fluorinated Amido Esters through Unexpected C3-C4 Bond Fission in 4-Trifluoromethyl-3-oxo-β-lactams
- Source :
- Chemistry, an Asian journal. 13(4)
- Publication Year :
- 2017
-
Abstract
- 4-Trifluoromethyl-3-oxo-β-lactams were unexpectedly transformed into 2-[(2,2-difluorovinyl)amino]-2-oxoacetates as major products, accompanied by minor amounts of 2-oxo-2-[(2,2,2-trifluoroethyl)amino]acetates, upon treatment with alkyl halides and triethylamine in DMSO. This peculiar C3-C4 bond fission reactivity was investigated in-depth, from both an experimental and a computational point of view, in order to shed light on the underlying reaction mechanism.
- Subjects :
- chemistry.chemical_classification
Reaction mechanism
Oxamic Acid
Trifluoromethyl
Molecular model
Molecular Structure
010405 organic chemistry
Trifluoromethylation
Organic Chemistry
Esters
General Chemistry
010402 general chemistry
beta-Lactams
01 natural sciences
Biochemistry
Medicinal chemistry
0104 chemical sciences
chemistry.chemical_compound
chemistry
Models, Chemical
Non-covalent interactions
Reactivity (chemistry)
Triethylamine
Alkyl
Subjects
Details
- ISSN :
- 1861471X
- Volume :
- 13
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Chemistry, an Asian journal
- Accession number :
- edsair.doi.dedup.....4a3b83cedd6f77d3699aa2e92428b86b