Allylation of quinones via photoinduced electron-transfer reactions from allylstannanes.
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概要
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Photochemical reactions of quinones with allylstannanes provided four types of products: adducts of allyl group to the carbonyl oxygens of quinones, adducts of allyl group to the olefinic carbons, adducts of allyl group to the carbonyl carbons, and hydroquinones. An electron-transfer mechanism was confirmed by <SUP>1</SUP>H-CIDNP (Chemically Induced Dynamic Nuclear Polarization) method. This study suggests that a) photoinduced electron transfer from allylstannanes to quinones produces the corresponding quinone anion radicals and tin cation radicals, b) the tin cation radicals cleave to give allyl radicals as well as tin cation, and c) the allyl radicals attack the quinone anion radicals resulting in the formation of final products, allylated quinones.
- 公益社団法人 日本化学会の論文
著者
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Imahori Hiroshi
Department Of Material And Life Science Graduate School Of Engineering Osaka University
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Maruyama Kazuhiro
Department Of Chemistry Faculty Of Science Kyoto University
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