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dc.contributor.authorZhou, Lin
dc.contributor.authorTimmermann, Barbara N.
dc.contributor.authorGrittini, Carina
dc.contributor.authorBruck, Michael A.
dc.contributor.authorEnemark, John H.
dc.date.accessioned2015-05-04T17:15:49Z
dc.date.available2015-05-04T17:15:49Z
dc.date.issued1996
dc.identifier.citationZhou, L., Timmermann, B.N., Grittini, C., Bruck, M.A., and Enemark, J.H. "Tarapacol 15-Acetate, a New Diterpenoid from Grindelia tarapacana Phil." Acta Cryst. (1996). C52, 1042-1044 http://dx.doi.org/10.1107/S0108270195013473en_US
dc.identifier.urihttp://hdl.handle.net/1808/17565
dc.description.abstractIn the title compound, 15-acetoxy-14(S)-hydroxy-13-epi-manoyl oxide {IUPAC systematic name: 2-(dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran-3-yl)-2-hydroxyethyl acetate}, C22H38N4, rings A and B have chair conformations. Ring C adopts a boat conformation with the 16-methyl group in an axial position and the bulky glycol monoacetate group in an equatorial position. Ring systems A/B and B/C (conventional IUPAC labdane diterpenoid nomenclature) are trans fused about the C(5)-C(10) and C(8)-C(9) bonds, respectively. The present study establishes the relative stereochemistry at the C(14) position.en_US
dc.description.sponsorshipThis work was supported by a grant to the American Association for the Advancement of Science from the John D. and Catherine T. MacArthur Foundation, awarded to BNT. The structure was determined in the Molecular Structure Laboratory of the Department of Chemistry as a special class project in Chemistry 517.en_US
dc.publisherInternational Union of Crystallographyen_US
dc.titleTarapacol 15-Acetate, a New Diterpenoid from Grindelia tarapacana Phil.en_US
dc.typeArticle
kusw.kuauthorTimmerman, Barbara N.
kusw.kudepartmentDepartment of Medical Chemistryen_US
dc.identifier.doi10.1107/S0108270195013473
kusw.oaversionScholarly/refereed, publisher version
kusw.oapolicyThis item does not meet KU Open Access policy criteria.
dc.rights.accessrightsopenAccess


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