
TY  - JOUR
A1  - Hillis, WE 
A1  - Horn, DHS 
T1  - Nuclear magnetic resonance spectra and structures of some C-glycosyl flavonoids
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1965
VL  - 18
IS  - 4
SP  - 531
EP  - 542
KW  - 
UR  - https://doi.org/10.1071/CH9650531 
N2  - From an examination of the nuclear magnetic resonance spectra, optical rotations, and other properties of a number of flavonoid C-glycosides, their acetates, and related model compounds, it is concluded that vitexin, bayin, puerarin, and isohemiphloin are C-&#946;-D-glucosides with the sugar substituent in the 8-position of the flavonoid nucleus. Hemiphloin and saponaretin are two of the corresponding 6-substituted compounds. In hemiphloin and isohemiphloin the phenyl B ring has the equatorial configuration. 
ER  -

