Publication Type:

Journal Article

Source:

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

URL:

http://www.tandfonline.com/doi/abs/10.1080/00397918508077260

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.

Cite this Research Publication

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

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