Jg. Rodriguez et al., MOLECULAR-STRUCTURE AND ABSOLUTE-CONFIGURATION OF TITHONIN, A HELIANGOLIDE FROM TITHONIA-ROTUNDIFOLIA, Journal of natural products, 58(3), 1995, pp. 446-449
The molecular structure and absolute configuration of tithonin [1], a
heliangolide isolated from Tithonia rotundifolia, have been determined
by X-ray diffraction analysis. Correlations between the position and
stereochemistry of the gamma-lactone ring fusion to the ten-membered r
ing and the sign of the Cotton effect of the n-pi transition of the C
=C-C=O chromophore of 1 have been analyzed.