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Synthesis of Cycloartocarpesin Trimethyl Ether

Publication Type : Journal Article

Thematic Areas : Biotech

Publisher : Taylor & Francis

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

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Campus : Amritapuri

School : School of Biotechnology

Center : Biotechnology, Phytochemistry Labs, Sanitation Biotechnology

Department : biotechnology

Year : 1985

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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