Verticine ethanol hydrate (2/1/1)
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AbstractThe two symmetry-independent molecules of the title compound, cevane-3 beta,6 alpha,20-triol ethanol hydrate (2/1/1), 2C(27)H(45)NO(3). C2H6O . H2O, have the same stereochemical assignments. The six-membered rings A, B, E and F are in the chair conformation, while ring D is in a boat conformation. The ring fusions are A/B trans, B/C trans, C/D cis, D/E trans and E/F trans. The verticine molecules are bridged by water and ethanol molecules via hydrogen bonds to form two-dimensional layers, and the crystal structure is built up by stacking of these layers.
All Author(s) ListZhang JN, Lin G, Ho YP, Li P, Chow AHL
Journal nameActa Crystallographica Section C: Crystal Structure Communications
Year2000
Month7
Day1
Volume Number56
PublisherWILEY-BLACKWELL
Pages907 - 909
ISSN0108-2701
eISSN1600-5759
LanguagesEnglish-United Kingdom
Web of Science Subject CategoriesChemistry; Chemistry, Multidisciplinary; Crystallography; CRYSTALLOGRAPHY

Last updated on 2020-22-11 at 23:50