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 › peer-review

13 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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title = "Tepanone, a retrochalcone from Ellipeia cuneifolia",

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.",

author = "S.M. Colegate and L.B. Din and Emilio Ghisalberti and A. Latiff",

year = "1992",

doi = "10.1016/0031-9422(92)80377-Q",

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T1 - Tepanone, a retrochalcone from Ellipeia cuneifolia

AU - Colegate, S.M.

AU - Din, L.B.

AU - Ghisalberti, Emilio

AU - Latiff, A.

PY - 1992

Y1 - 1992

N2 - 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.

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.

U2 - 10.1016/0031-9422(92)80377-Q

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

M3 - Article

VL - 31

SP - 2123

EP - 2126

JO - Phytochemistry

JF - Phytochemistry

IS - 6

ER -

Tepanone, a retrochalcone from Ellipeia cuneifolia

Abstract

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