کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1314327 | 1499367 | 2012 | 7 صفحه PDF | دانلود رایگان |
A series of fluorinated propargylamines have been synthesized from the one-pot three-component reaction of fluorobenzaldehyde, aniline and phenylacetylene under solvent-free and microwave irradiation. The fluorinated propargylamines were then further transformed to chalcones or quinoline derivatives respectively depending on the different structures of propargylamines.
A series of fluorinated propargylamines have been synthesized from the one-pot three-component reaction of fluorobenzaldehyde, aniline and phenylacetylene under solvent-free and microwave irradiation. The fluorinated propargylamines were then further transformed to chalcones or quinoline derivatives respectively depending on the different structures of propargylamines.Figure optionsDownload as PowerPoint slideHighlights
► A one-pot solvent-free microwave irradiation reaction was investigated.
► A series of fluorinated propargylamines have been synthesized.
► The products were further transformed to chalcones or quinolines.
► The possible mechanism was proposed.
Journal: Journal of Fluorine Chemistry - Volume 133, January 2012, Pages 139–145