Publication Type : Journal Article
Thematic Areas : Biotech
Publisher : Taylor & Francis
Source : Synthetic Communications, Taylor & Francis, Volume 15, Number 13, p.1165–1170 (1985)
Url : http://www.tandfonline.com/doi/abs/10.1080/00397918508077260
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.