کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1314785 | 1499354 | 2013 | 6 صفحه PDF | دانلود رایگان |

The insertion of fluorinated 1,3-dicarbonyl compounds to benzyne resulted in regioselective formation of various fluorinated 1,5-dicarbonyl compounds which are not readily available by other methods. Products include 2-trifluoroacetyl- and 2-(perfluoroalkanoyl)phenylacetic estres, 2-fluoro-2-phenylacetic esters, 1-aryl-2-(2-trifluoroacetylphenyl)ethan-1-ones and other derivatives.
2-Trifluoroacetyl- and 2-(perfluoroalkanoyl)phenylacetic estres, 2-fluoro-2-phenylacetic esters, 1-aryl-2-(2-trifluoroacetylphenyl)ethan-1-ones and other fluorinated 1,5-dicarbonyl compounds areregioselectively prepared by insertion of fluorinated 1,3-dicarbonyl compounds to benzyne.Figure optionsDownload as PowerPoint slideHighlights
► The first insertions of fluorinated 1,3-dicarbonyl compounds to benzyne are reported.
► Reactions proceed with very good regioselectivity.
► Fluorinated 1,5-dicarbonyl compounds which are not readily available by other methods are prepared.
Journal: Journal of Fluorine Chemistry - Volume 146, February 2013, Pages 80–85