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- W2041575210 abstract "The electron-transfer photochemistry of homochrysanthemol, 1, resulted exclusively in intramolecular substitution at the quaternary cyclopropane carbon, generating the five-membered cyclic ethers, 2 and 4. The alternative addition to the terminal carbon of the double bond, which would result in seven-membered cyclic ethers, 3 and 5, was not observed. Apparently, the five-membered transition state leading to 2 and 4 is significantly favored over the seven-membered one required for formation of 3 and 5. These results stand in interesting contrast to the previously established reaction pattern of chrysanthemol, 8, which is captured exclusively at the terminal vinyl carbon. The divergent regiochemistry of 1(*)(+) and 8(*)(+) (even though the tethers between vinylcyclopropane and alcohol functions differ only by a single CH(2) group) elucidates the principles governing the course of nucleophilic capture in radical cations." @default.
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- W2041575210 date "1999-04-29" @default.
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- W2041575210 title "Electron Transfer Photochemistry of Homochrysanthemol: Intramolecular Nucleophilic Attack on the Cyclopropane Ring" @default.
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- W2041575210 doi "https://doi.org/10.1021/jo9903048" @default.
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