| Literature DB >> 26396907 |
Andreas Schäfer1, Christopher Golz1, Hans Preut1, Carsten Strohmann1, Martin Hiersemann1.
Abstract
The title hydrate, C17H28O2·H2O, was synthesized in order to determine the relative configuration of the tetra-cyclic framework. The fused 5,6,7-tricarbocyclic core exhibits an entire cis-annulation, featuring a 1,4-cis-relation of the angular methyl groups in the six-membered ring. The oxa bridge of the ep-oxy-cyclo-heptane moiety is oriented towards the concave face of the boat-shaped mol-ecule, whereas the angular methyl groups are directed towards the convex face. The asymmetric unit of the crystal contains two nearly identical formula units, which are related via a pseudo-centre of symmetry. The structure could be solved in the space groups I-4 and I41/a. The refinement in the acentric space group, however, gave significantly better results and these are used in this paper. O-H⋯O hydrogen bonds are observed between the organic mol-ecules, between the organic mol-ecules and the water mol-ecules, and between the water mol-ecules, forming a chain along the c-axis direction.Entities:
Keywords: crystal structure; diterpenoid synthesis; hydrate; hydrogen bonding
Year: 2015 PMID: 26396907 PMCID: PMC4555390 DOI: 10.1107/S2056989015015698
Source DB: PubMed Journal: Acta Crystallogr E Crystallogr Commun