@article{oai:kanazawa-u.repo.nii.ac.jp:00010823,
 author = {前多, 肇 and 千木, 昌人 and 添田, 貴宏 and 宇梶, 裕 and Watanabe, Yasutaka and Sakai, Takahiro and Maeda, Hajime and Segi, Masahito and Soeta, Takahiro and Ukaji, Yutaka},
 issue = {2},
 journal = {Heterocycles},
 month = {Sep},
 note = {Magnesium-alkoxide directed photoaddition of tetrahydrofurans to γ,γ-disubstituted allylic alcohols was achieved. When the allylic alcohols were treated with Grignard reagent in THF under light, the corresponding γ-(2-tetrahydrofuryl) substituted alcohols were regioselectively obtained in up to 82% yield. The conversion of the hydroxyl group to the corresponding bromomagnesium alkoxide was crucial., Embargo Period 24 months},
 pages = {833--844},
 title = {Magnesium-Alkoxide Directed Photoaddition of Tetrahydrofurans to γ,γ-Disubstituted Allylic Alcohols},
 volume = {93},
 year = {2016}
}