The reaction of β-dicarbonyl compounds with trifluoromethyl-sulphenyl chloride. I: CF3S-substituted esters, anilides of β-keto acids, and their Schiff bases: synthesis and stability
- Author
- KOLASA, A1
[1] Jagiellonian univ., dep. organic chemistry, Cracow 30060, Poland - Source
Journal of fluorine chemistry. 1987, Vol 36, Num 1, pp 29-40 ; ref : 21 ref
- CODEN
- JFLCAR
- ISSN
- 0022-1139
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier Sequoia, Lausanne
- Publication country
- Switzerland
- Document type
- Article
- Language
- English
- Keyword (fr)
- Alkylthiolation Composé aliphatique Composé saturé Cétimine Cétoamide Cétoester Cétosulfure Halogénure sulfényle Solution aqueuse Acétone(trifluorométhylthio) Acétophénone(trifluorométhylthio-«2») Acétylacétique acide(trifluorométhylthio-«2») ester éthyle Acétylacétique acide,ester éthyle Acétylacétique acide,phénylamide Benzènepropionique acide(«β»oxo «α»-trifluorométhylthio) phénylamide Benzènepropionique acide(β-oxo) ester éthyle Butyrique acide(phénylimino-«3») phénylamide DMSO Méthanesulfénique acide(trifluoro) chlorure
- Keyword (en)
- Alkylthiolation Aliphatic compound Saturated compound Ketimine Ketoamide Ketoester Ketosulfide Sulfenyl halide Aqueous solution
- Keyword (es)
- Alquiltiolación Compuesto alifatico Compuesto saturado Cetimina Cetoamida Cetoester Cetosulfuro Halogenuro sulfenilo Solucion acuosa
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C03 Noncondensed benzenic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8343179
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/S0022-1139(00)82051-5 
https://dx.doi.org/10.1016/S0022-1139(00)82051-5
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