ol7b01431_si_002.cif (285.94 kB)

Iron-Catalyzed Oxidative C–H Functionalization of Internal Olefins for the Synthesis of Tetrasubstituted Furans

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posted on 01.06.2017, 11:48 by Jiang Lou, Quannan Wang, Kaikai Wu, Ping Wu, Zhengkun Yu
Tetrasubstituted furans were efficiently synthesized from Fe­(OAc)2-catalyzed C–H/C–H cross-dehydrogenative-coupling (CDC) reactions of activated carbonyl methylenes with S,S-functionalized internal olefins, that is, α-oxo ketene dithioacetals and analogues, under oxidative conditions. β-Ketoesters, 1,3-dicarbonyls, β-keto nitrile, and amide derivatives were used as the coupling partners. The resultant alkylthio- and carbonyl-functionalized furans could be further transformed to diverse arylated furan derivatives and furan-fused N-heterocycles, respectively. The control experiments have revealed a radical reaction pathway.

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