Fun Hoong-Kun, Joycharat Nantiya, Voravuthikunchai Supayang Piyawan, Chantrapromma Suchada
Acta Crystallogr Sect E Struct Rep Online. 2010 Mar 20;66(Pt 4):o879-80. doi: 10.1107/S1600536810009499.
The title seco-dammarane triterpenoid, C(27)H(42)O(4) (systematic name: 3-{(3S,3aR,5aR,6S,7S,9aR,9bR)-6,9a,9b-trimethyl-3-[(R)-2-methyl-5-oxotetra-hydro-furan-2-yl]-7-(prop-1-en-2-yl)dodeca-hydro-1H-cyclo-penta-[a]naphthalen-6-yl}propanoic acid), has been isolated for the first time from the seeds of Aglaia forbesii. The mol-ecule has three fused rings and all rings are in trans-fused. The two cyclo-hexane rings are in standard chair conformations and the cyclo-pentane ring adopts an envelope conformation. Its absolute configuration was determined by the refinement of the Flack parameter to 0.26 (17). In the crystal, mol-ecules are linked into chains along [010] by O-H⋯O hydrogen bonds.
标题化合物裂环达玛烷三萜,化学式为C(27)H(42)O(4)(系统命名:3 - {(3S,3aR,5aR,6S,7S,9aR,9bR)-6,9a,9b - 三甲基 - 3 - [(R)-2 - 甲基 - 5 - 氧代四氢呋喃 - 2 - 基]-7 - (丙 - 1 - 烯 - 2 - 基)十二氢 - 1H - 环戊[a]萘 - 6 - 基}丙酸),首次从福氏米仔兰种子中分离得到。该分子有三个稠合环,且所有环均为反式稠合。两个环己烷环呈标准椅式构象,环戊烷环呈信封式构象。其绝对构型通过将Flack参数精修至0.26 (17)确定。在晶体中,分子通过O - H⋯O氢键沿[010]方向连接成链。