Acanthoic acid

Autor: Sunisa Suwancharoen, Wantanee Tommeurd, Chuttree Phurat, Nongnuj Muangsin, Surachai Pornpakakul
Jazyk: angličtina
Rok vydání: 2010
Předmět:
Zdroj: Acta Crystallographica Section E, Vol 66, Iss 7, Pp o1531-o1531 (2010)
Druh dokumentu: article
ISSN: 16005368
1600-5368
DOI: 10.1107/S1600536810019483
Popis: 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.
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