{"database":"biostudies-literature","file_versions":[],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":51,"searchCount":0},"additional":{"submitter":["Sloman DL"],"funding":["NCI NIH HHS"],"pagination":["9952-5"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3134420"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["133(26)"],"pubmed_abstract":["Kibdelones are hexacyclic tetrahydroxanthones and potent anticancer agents isolated from an Australian microbe. Herein, we describe the synthesis of a chiral, nonracemic iodocyclohexene carboxylate EF ring fragment of the kibdelones employing an intramolecular iodo halo-Michael aldol reaction and its merger with an ABCD ring fragment to afford the congener kibdelone C."],"journal":["Journal of the American Chemical Society"],"pubmed_title":["Total synthesis and absolute stereochemical assignment of kibdelone C."],"pmcid":["PMC3134420"],"funding_grant_id":["R01 CA137270-01A1","R01 CA137270-02","R01 CA137270"],"pubmed_authors":["Bacon JW","Sloman DL","Porco JA"],"view_count":["51"],"additional_accession":[]},"is_claimable":false,"name":"Total synthesis and absolute stereochemical assignment of kibdelone C.","description":"Kibdelones are hexacyclic tetrahydroxanthones and potent anticancer agents isolated from an Australian microbe. Herein, we describe the synthesis of a chiral, nonracemic iodocyclohexene carboxylate EF ring fragment of the kibdelones employing an intramolecular iodo halo-Michael aldol reaction and its merger with an ABCD ring fragment to afford the congener kibdelone C.","dates":{"release":"2011-01-01T00:00:00Z","publication":"2011 Jul","modification":"2024-11-13T16:25:19.869Z","creation":"2019-03-27T03:06:59Z"},"accession":"S-EPMC3134420","cross_references":{"pubmed":["21648477"],"doi":["10.1021/ja203642n"]}}