Synlett 2012; 23(14): 2059-2062
DOI: 10.1055/s-0032-1316585
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© Georg Thieme Verlag Stuttgart · New York

Aerobic Photooxidative Cleavage of Vicinal Diols to Carboxylic Acids Using 2-Chloroanthraquinone

Yoko Matsusaki
Gifu Pharmaceutical University, 1-25-4, Daigaku-nishi, Gifu 501-1196, Japan, Fax: +81(58)2308108   eMail: itoha@gifu-pu.ac.jp
,
Tomoaki Yamaguchi
Gifu Pharmaceutical University, 1-25-4, Daigaku-nishi, Gifu 501-1196, Japan, Fax: +81(58)2308108   eMail: itoha@gifu-pu.ac.jp
,
Norihiro Tada
Gifu Pharmaceutical University, 1-25-4, Daigaku-nishi, Gifu 501-1196, Japan, Fax: +81(58)2308108   eMail: itoha@gifu-pu.ac.jp
,
Tsuyoshi Miura
Gifu Pharmaceutical University, 1-25-4, Daigaku-nishi, Gifu 501-1196, Japan, Fax: +81(58)2308108   eMail: itoha@gifu-pu.ac.jp
,
Akichika Itoh*
Gifu Pharmaceutical University, 1-25-4, Daigaku-nishi, Gifu 501-1196, Japan, Fax: +81(58)2308108   eMail: itoha@gifu-pu.ac.jp
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Publikationsverlauf

Received: 14. Mai 2012

Accepted after revision: 07. Juni 2012

Publikationsdatum:
26. Juli 2012 (online)


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Abstract

We developed the aerobic photooxidative cleavage of vicinal diols to carboxylic acids using 2-chloroanthraquinone in the presence of photoirradiation with a high-pressure mercury lamp. This is the first metal-free reaction using molecular oxygen as the terminal oxidant.