Facile synthesis of both linear and angular triquinanes from the tricyclo[5.4.0.01,5]undec-9-ene-8,11-dione efficiently produced by a combination of electro- and photochemical reactions

Maki, Shôjirô; Toyoda, K.; Mori, Takeshi; Kosemura, Seiji; Yamamura, Shosuke

doi:10.1016/s0040-4039(00)76976-0

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A Reactions Of Alkenes With Alkanoic Acids1

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2009

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Cited by 11 publications

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“…159 b. Reactions of alkenes with 1,3-dicarbonyl and related compounds Radical adducts formed by ethyl acetoacetate, diethyl malonate or malononitrile with vinyl ethyl ether or styrene are oxidised at the anode to cationic intermediates, which react with external or internal nucleophiles being thus converted into linear (108,109) and/or cyclic products (110,111). The adducts formed with styrene also give dimers 112.…”

Section: A Reactions Of Alkenes With Alkanoic Acidsmentioning

confidence: 99%