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- W2953057608 abstract "Oxidative cycloaddition of a 2-cyclohexenone or α-tetralone and an alkene with dried Mn(OAc)3 in benzene at 80−140 °C provides a general route to dihydrobenzofurans 15 and dihydronaphthofurans 17. Although the yields are modest, this one-pot reaction provides simple access to these compounds, which have previously been prepared by multistep routes. Oxidative cycloaddition of 2-cyclohexenones with β-methylstyrenes provides a new route to benzofuranoid neolignans, which was applied to the synthesis of conocarpan (22). The formation of 2-acetoxyhexanedioic acids 27 and 47 from acetoxylation of 2-cyclohexenones in HOAc, but not in benzene, opens up a new class of Mn(OAc)3 reactions and explains Watt and Demir's discovery that much higher yields of α‘-acetoxy enones are obtained in benzene than in HOAc." @default.
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- W2953057608 date "1997-10-01" @default.
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- W2953057608 title "Synthesis of 2,3-Dihydrobenzofurans by Mn(OAc)<sub>3</sub>-Based Oxidative Cycloaddition of 2-Cyclohexenones with Alkenes. Synthesis of (±)-Conocarpan" @default.
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- W2953057608 doi "https://doi.org/10.1021/jo9708506" @default.
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