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Atom-Economical and Metal-Free Synthesis of Multisubstituted Furans from Intramolecular Aziridine Ring Opening

机译:分子内氮丙啶环的开环原子取代和无金属合成多取代基呋喃

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Multisubstituted furans were prepared from dialkyl 2-(aziridin-2-ylmethylene)malonate and/or 1,3-dione through aziridine ring opening by the internal carbonyl oxygen with the assistance of BF_(3)·OEt_(2), followed by aromatization. This synthetic method is free from any metal and is atom-economical with all of the atoms in the starting material retained in the final product.
机译:在BF_(3)·OEt_(2)的辅助下,通过内部羰基氧通过氮丙啶开环,由2-(叠氮基-2-基亚甲基)丙二酸二烷基酯和/或1,3-二酮制备多取代基的呋喃。 。这种合成方法不含任何金属,并且经济实惠,原材料中的所有原子都保留在最终产品中。

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