Nuclear oxidation in flavones and related compounds - Part XXXIV. Para-oxidation in the side-phenyl nucleus: Preparation of 6′-hydroxy-myricetin
K J Balakrishna N Prabhakara Rao T R Seshadri
Click here to view fulltext PDF
Permanent link:
https://www.ias.ac.in/article/fulltext/seca/033/03/0151-0154
Para oxidation in the side-phenyl nucleus has now been investigated using potassium persulphate and 3′-hydroxy-3:5:7:4′:5′-pentamethoxy flavone obtained conveniently from cannabiscitrin. The resulting quinol on methylation yields 3:5:7:3′:4′:5′:6′-heptamethoxy flavone and on demethylation 6′-hydroxy myricetin which is the first example of a flavone having four hydroxyl groups in the side-phenyl nucleus.
K J Balakrishna1 N Prabhakara Rao1 T R Seshadri1
© 2021-2022 Indian Academy of Sciences, Bengaluru.