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- W2950356859 abstract "We report a new synthesis and our study of the mechanism of formation of substituted 1-trifluoromethyl and 1-perfluoroalkyl-3-(phenylamino)prop-2-en-1-one starting from 3-(R-phenoxy)-3-perfluoroalkyl-prop-2-enals and arylamines. Reactivity study of the intermediates confirmed that 3-perfluoroalkyl-N,N′-diphenyl-1,5-diazapentadienes are the synthetic intermediates of the synthesis of 2-perfluoroalkylquinolines. The mechanism of the reaction of 1-trifluoromethyl and 1-perfluoroalkyl-3-(phenylamino)prop-2-en-1-one with POCl3 was studied. To our knowledge this is the first detection and isolation of N,N′-diaryldiazapentadiene derivatives as intermediates in the Combes F-alkyl substituted quinoline synthesis starting from enaminoketones. Finally, we succeeded isolating and identifying unsymmetrically substituted 2-perfluorolakyldiazapentadiene." @default.
- W2950356859 created "2019-06-27" @default.
- W2950356859 creator A5007675085 @default.
- W2950356859 creator A5019291198 @default.
- W2950356859 creator A5042460842 @default.
- W2950356859 date "2014-02-01" @default.
- W2950356859 modified "2023-10-10" @default.
- W2950356859 title "Synthesis of substituted 1-trifluoromethyl and 1-perfluoroalkyl-3-(arylamino)prop-2-en-1-one: advances in the mechanism of Combes 2-trifluoromethyl and 2-perfluoroalkyl quinolines synthesis" @default.
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- W2950356859 doi "https://doi.org/10.1016/j.tet.2013.12.073" @default.
- W2950356859 hasPublicationYear "2014" @default.
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