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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 15, 1985 - Issue 13
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Original Articles

Synthesis of Cycloartocarpesin Trimethyl Ether

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Pages 1165-1170 | Published online: 19 Dec 2006
 

Abstract

The synthesis of chromenoflavone, cycloartocarpesin trimethyl ether (1b) has been achieved through the aroylation of lithium enolate of evodionol (2) with 2,4-dimethoxybenzoyl chloride followed by cyclodehydration of the β-diketone (3) with D-toluenesulphonic acid.

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