Publication Type : Journal Article
Thematic Areas : Biotech
Publisher : Letters in Organic Chemistry
Source : Letters in Organic Chemistry, vol. 11, pp. 225–229, 2014.
Campus : Amritapuri, Coimbatore
School : School of Physical Sciences, School of Biotechnology
Center : Biotechnology, Phytochemistry Labs
Department : Department of Sciences, biotechnology, Chemistry
Year : 2014
Abstract : Baker-Venkataraman (BV) rearrangement is the method of choice for the synthesis of flavones. The major limitation of BV is that it requires extensive protections and deprotections of hydroxyl groups which make the process lengthy and cumbersome. In the present study, a three step efficient method has been developed using simple protecting groups and easily available starting materials. New syntheses for acacetin, chrysoeriol, diosmetin, tricin and other hydroxylated flavones are described. - See more at: http://www.eurekaselect.com/120227/article#sthash.yQrZK0AA.dpuf
Cite this Research Publication : Pandurangan Nanjan and Dr. Asoke Banerji, “A new synthesis for acacetin, chrysoeriol, diosmetin, tricin and other hydroxylated flavones by modified baker-venkataraman transformation”, Letters in Organic Chemistry, vol. 11, pp. 225–229, 2014.