Carbon-13 NMR Chemical Shift of Methyl Group: A Useful Parameter for Structural Analysis of C-Methylated Flavonoids
2006 ◽
Vol 1
(11)
◽
pp. 1934578X0600101
Keyword(s):
Group A
◽
The 13C NMR resonances corresponding to the C-Me group of C-6 and/or C-8 C-methylated-flavonoids absorb between 6.7–10.0 ppm and typically between 6.7–8.7 ppm. A comparative 13C NMR study reflects that the 13C NMR chemical shifts reported for 6-hydroxy-5-methyl-3′,4′,5′-trimethoxyaurone-4-O-α-L-rhamnoside from Pterocarpus santalinus and 8-C-methyl-5,7,2′,4′- tetramethoxyflavanone from Terminalia alata are inconsistent with the assigned structures, and therefore need reconsideration.
2001 ◽
Vol 14
(3)
◽
pp. 166-171
◽
2017 ◽
Vol 16
(2)
◽
pp. 147-151
◽
Keyword(s):
1980 ◽
Vol 45
(10)
◽
pp. 2772-2778
◽
Keyword(s):