Synthesis of 2′,3′,4,4′,6′-Pentahydroxychalcone, an Aglycone of Carthamin, and Its Isomerization into 4′,5,6,7- and 4′,5,7,8-Tetrahydroxyflavanone, Carthamidin and Isocarthamidin
- 1 December 1978
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 51 (12) , 3627-3630
- https://doi.org/10.1246/bcsj.51.3627
Abstract
2′,3′,4,4′,6′-Pentahydroxychalcone (4), an aglycone of carthamin, was synthesized by the demethoxymethylation of 2′,3′,4,4′,6′-pentakis(methoxymethoxy)chalcone prepared by the condensation of 2,3,4,6-tetrakis(methoxymethoxy)acetophenone with p-methoxymethoxybenzaldehyde. 4 was converted into 4′,5,6,7- and 4′,5,7,8-tetrahydroxyflavanone (5 and 6) by boiling with methanolic hydrochloric acid. On the basis of the comparisons of the properties of 5 and 6 with those of carthamidin (A) and isocarthamidin (B) derived from natural product, the structures originally assigned for A and B should be reversed.This publication has 3 references indexed in Scilit:
- 4′,5,6,7-Oxygenated Flavones and FlavanonesJournal of Pharmaceutical Sciences, 1964
- Synthetic experiments in the benzopyrone seriesProceedings of the Indian Academy of Sciences - Section A, 1949
- Carthamin. INIPPON KAGAKU KAISHI, 1930