Publication Type:

Journal Article


Synthetic Communications, Taylor & Francis, Volume 15, Number 13, p.1165–1170 (1985)



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.

Cite this Research Publication

A. Banerji and Goomer, N. C., “Synthesis of Cycloartocarpesin Trimethyl Ether”, Synthetic Communications, vol. 15, pp. 1165–1170, 1985.