Oxidative Trimerization of Catechol to Hexahydroxytriphenylene | Zendy

Morimoto Koji | Zendy; Dohi Toshifumi | Zendy; Kita Yasuyuki | Zendy

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Oxidative Trimerization of Catechol to Hexahydroxytriphenylene

Author(s) -

Morimoto Koji,

Dohi Toshifumi,

Kita Yasuyuki

Publication year - 2013

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201201515

Subject(s) - hypervalent molecule , chemistry , catechol , oxidative coupling of methane , reagent , oxidative phosphorylation , iodine , green chemistry , environmentally friendly , organic chemistry , combinatorial chemistry , catalysis , reaction mechanism , biochemistry , ecology , biology

Direct oxidative coupling is an attractive tool for environmentally benign green chemistry. We report the novel oxidative synthesis of hexahydroxytriphenylene by using a hypervalent iodine reagent. The reaction proceeds under very mild conditions for reducing acid waste and in a very short time at room temperature.

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