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Issue 13, 2000
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Facile construction of the oxaphenalene skeleton by peri ring closure. Formal synthesis of mansonone F

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Abstract

A concise and divergent total synthesis of mansonone F has been accomplished via an efficient construction of the oxaphenalene skeleton by facile peri ring closure of the naphthol ether, and an effective preparation of the cyclization precursor starting from readily available 5-methoxy-1-tetralone by employing a palladium-induced aromatization of the naphthalinol.

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Publication details

The article was received on 07 Mar 2000, accepted on 16 May 2000 and first published on 15 Jun 2000


Article type: Communication
DOI: 10.1039/B001859G
Citation: Chem. Commun., 2000,0, 1203-1204

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    Facile construction of the oxaphenalene skeleton by peri ring closure. Formal synthesis of mansonone F

    Y. Suh, D. Shin, K. Min, S. Hyun, J. Jung and S. Seo, Chem. Commun., 2000, 0, 1203
    DOI: 10.1039/B001859G

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