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Generation of Radical Species from Cyclohexane-1,2-dione and the Reaction with Olefins : Preparation of 4,5-Dihydro-7(6H)-benzofuranone Derivatives

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Title: Generation of Radical Species from Cyclohexane-1,2-dione and the Reaction with Olefins : Preparation of 4,5-Dihydro-7(6H)-benzofuranone Derivatives
Authors: Miura, Masanori Browse this author
Arai, Noriyoshi Browse this author →KAKEN DB
Narasaka, Koichi Browse this author
Issue Date: 1998
Publisher: Chemical Society of Japan
Journal Title: Bulletin of the Chemical Society of Japan
Volume: 71
Issue: 6
Start Page: 1437
End Page: 1441
Publisher DOI: 10.1246/bcsj.71.1437
Abstract: Oxidation of cyclohexane-1,2-dione with ammonium hexanitratocerate(IV) (CAN) generates 2,3-dioxocyclohexyl radical, which reacts with electron-rich olefins to afford the corresponding addition products. The adducts thus generated are converted to 4,5-dihydro-7(6H)-benzofuranone by acid treatment. In addition to cyclohexane-1,2-dione, radical species are also generated from cyclopentane-1,2-dione and cycloheptane-1,2-dione.
Type: article
URI: http://hdl.handle.net/2115/70768
Appears in Collections:工学院・工学研究院 (Graduate School of Engineering / Faculty of Engineering) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 新井 則義

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