Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Synthetic Studies on the Flavone Derivatives. XIII. Synthesis of Flavones with Tetramethoxyl Groups in Ring B
MUNEKAZU IINUMATOSHIYUKI TANAKASHIN MATSUURA
Author information
Keywords: ^<13>C-NMR
JOURNAL FREE ACCESS

1984 Volume 32 Issue 9 Pages 3354-3360

Details
Abstract
2', 3', 4', 5, 5', 6, 7, 8-Octamethoxy-(Ia) and 2', 3', 4', 5, 5', 6, 7-heptamethoxyflavone (IIa) and their position isomers substituted with tetramethoxyl groups in ring B were synthesized to confirm the structures of agehoustin A and agehoustin B isolated from Ageratum houstonianum. The characteristics of the synthesized flavones were investigated by spectroscopic methods.
Content from these authors
© The Pharmaceutical Society of Japan
Previous article Next article
feedback
Top