Abstract
The crystal and molecular structure of the natural product Zoapatanolide B has been determined by X-ray crystallographic analysis. The compound, obtained from the leaves ofMontanoa tomentosa, is a heliangolide sesquiterpene lactone. The two molecules of the asymmetric unit are linked together by hydrogen bonding and this results in conformational differences when the ester side chains (at C(9)) are compared.
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Cowe, H.J., Cox, P.J. & Alan Howie, R. Crystal and molecular structure of Zoapatanolide B, a sesquiterpene lactone. Journal of Crystallographic and Spectroscopic Research 20, 571–576 (1990). https://doi.org/10.1007/BF01221899
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DOI: https://doi.org/10.1007/BF01221899