Tepanone, a retrochalcone from Ellipeia cuneifolia

S.M. Colegate; L.B. Din; Emilio Ghisalberti; A. Latiff

doi:10.1016/0031-9422(92)80377-Q

Tepanone, a retrochalcone from Ellipeia cuneifolia

S.M. Colegate, L.B. Din, Emilio Ghisalberti, A. Latiff

School of Molecular Sciences

Research output: Contribution to journal › Article

11 Citations (Scopus)

Abstract

Tepanone, (2E)-1-phenyl-3-(2-hydroxy-3,4,6-trimethoxyphenyl)prop-2-enone was isolated from roots and stembark of Ellipeia cuneifolia. The structure was deduced from spectroscopic data and confirmed by synthesis of the methylated derivative, methyltepanone. Methyltepanone exists as the two readily interconvertible trans and cis isomers.

Original language	English
Pages (from-to)	2123-2126
Journal	Phytochemistry
Volume	31
Issue number	6
DOIs	https://doi.org/10.1016/0031-9422(92)80377-Q
Publication status	Published - 1992

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Colegate, S. M., Din, L. B., Ghisalberti, E., & Latiff, A. (1992). Tepanone, a retrochalcone from Ellipeia cuneifolia. Phytochemistry, 31(6), 2123-2126. https://doi.org/10.1016/0031-9422(92)80377-Q

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AB - Tepanone, (2E)-1-phenyl-3-(2-hydroxy-3,4,6-trimethoxyphenyl)prop-2-enone was isolated from roots and stembark of Ellipeia cuneifolia. The structure was deduced from spectroscopic data and confirmed by synthesis of the methylated derivative, methyltepanone. Methyltepanone exists as the two readily interconvertible trans and cis isomers.

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DO - 10.1016/0031-9422(92)80377-Q

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