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• W2028485764 abstract "A concise and diversity-oriented route to trifluoromethylbenzo[b]furans has been devised. A variety of phenols are directly converted to the corresponding 2-methylthio-3-trifluoromethylbenzo[b]furans by new triflic-anhydride-mediated extended Pummerer annulation reactions with trifluoromethylketene dithioacetal monoxide. The methylthio group of the products undergoes further transformations, which increase the diversity of available trifluoromethylbenzo[b]furans." @default.
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• W2028485764 date "2010-08-05" @default.
• W2028485764 modified "2023-10-17" @default.
• W2028485764 title "Synthesis of 3-Trifluoromethylbenzo[<i>b</i>]furans from Phenols via Direct <i>Ortho</i> Functionalization by Extended Pummerer Reaction" @default.
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• W2028485764 doi "https://doi.org/10.1021/ja1030134" @default.
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