Supplemental Observations on Atropisomerism of Fungal Bis(naphtho-y-pyrone)s

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Abstract

Epimerization reactions of bis(naphtho-y-pyrone) derivatives, ustilaginoidin A (2) and dihydroisoustilaginoidin A (6), were examined by refluxing the compounds in acetic acid and in p-xylene. The epimerization occurred in acetic acid but not in p-xylene. From the reaction mixture in the case of dihydroisoustilaginoidin A, the starting material and the epimer at the biaryl linkage, dihydroustilaginoidin A (7), were isolated and characterized. The circular dichroism Cotton effects due to chiral exciton coupling of biaryl compounds is discussed. © 1990, The Pharmaceutical Society of Japan. All rights reserved.

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Koyama, K., Aida, S., & Natori, S. (1990). Supplemental Observations on Atropisomerism of Fungal Bis(naphtho-y-pyrone)s. Chemical and Pharmaceutical Bulletin, 38(8), 2259–2261. https://doi.org/10.1248/cpb.38.2259

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