Issue 13, 2000

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

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.

Article information

Article type
Communication
Submitted
07 Mar 2000
Accepted
16 May 2000
First published
15 Jun 2000

Chem. Commun., 2000, 1203-1204

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, 1203 DOI: 10.1039/B001859G

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