[HTML version][PDF version][CIF][3d view][Structure Factors][Supplementary Material][CIF check Report][Issue contents]  [Open access]

[Contents scheme]

Acta Cryst. (2010). E66, o1531  [ doi:10.1107/S1600536810019483 ]

Acanthoic acid

S. Suwancharoen, W. Tommeurd, C. Phurat, N. Muangsin and S. Pornpakakul

Abstract: The title compound [systematic name: (1R,4aR,7S,8aS,10aS)-1,4a,7-trimethyl-7-vinyl-1,2,3,4,4a,6,7,8,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylic acid], C20H30O2, is a pimarane-type diterpene extracted from Croton oblongifolius. There are two independent molecules in the asymmetric unit. In both of these, the six-membered rings A, B and C adopt chair, boat and half-chair conformations, respectively. Rings A and B are trans-fused. The two molecules in the asymmetric unit form O-H...O hydrogen-bonded R22(8) dimers. The absolute configuration was assigned on the basis of the published literature on analogous structures.

Online 5 June 2010


Copyright © International Union of Crystallography
IUCr Webmaster