(+)-Cedrol hemihydrate: a natural product derived from drying eastern red cedar (Juniperus virginiana) wood

Bryan C. Chakoumakos, Xiaoping Wang

Research output: Contribution to journalArticlepeer-review

Abstract

Cedrol-like compounds are of pharmacological interest due to their diverse range of medicinal effects and are used globally in traditional medicines and cosmetics. Many cedrol tautomers are known from molecular studies but few have been studied in crystalline form by X-ray diffraction. Acicular white crystals collected from the wood of eastern red cedar (Juniperus virginiana) are determined to be (+)-cedrol hemihydrate, namely, (1S,2R,5S,7R,8R)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undecan-8-ol hemihydrate, C15H26O·0.5H2O, a novel packing of two unique cedrol molecules (Z' = 2) with a single water molecule [space group P212121; a = 6.1956 (1), b = 14.5363 (1), and c = 30.9294 (4) Å]. The hydrogen bonding forms a one-dimensional spiral chain running along the a axis, following the chirality of the cedrol molecule, through hydrogen-bonding interactions with a right-handed helical configuration in graph-set notation Δ - [Formula presented](6) > a > c > b. The crystal packing and symmetry are different from crystalline isocedrol due to the different hydrogen-bonding geometry.

Original languageEnglish
Pages (from-to)43-48
Number of pages6
JournalActa Crystallographica Section C: Structural Chemistry
Volume80
DOIs
StatePublished - Jan 28 2024

Funding

A portion of this work used resources at the Spallation Neutron Source, a DOE Office of Science User Facility operated by the Oak Ridge National Laboratory. Andrey Kovalevsky assisted with the X-ray data collection.

FundersFunder number
Office of Science
Oak Ridge National Laboratory

    Keywords

    • cedrol
    • chirality
    • crystal structure
    • eastern red cedar
    • hydrogen bonding
    • pharmacological interest
    • spiral chain
    • traditional medicine
    • tricyclic sesquiterpene

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