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pubmed-article:19117487pubmed:abstractTextInspired by the common skeletal motifs of Ca(2+)-ATPases inhibitors involving artemisinin and transtaganolide D, small molecule collections with the three-dimensional structural diversity of tricyclic systems were designed and expeditiously synthesized (4-5 steps). A synthetic strategy featuring stereochemical diversification of ring-junctions and control of cyclization modes was devised to access varied molecular architectures in a systematic fashion.lld:pubmed
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pubmed-article:19117487pubmed:authorpubmed-author:OguriHirokiHlld:pubmed
pubmed-article:19117487pubmed:authorpubmed-author:YamagishiYuta...lld:pubmed
pubmed-article:19117487pubmed:authorpubmed-author:OikawaHideaki...lld:pubmed
pubmed-article:19117487pubmed:authorpubmed-author:HirumaTakahis...lld:pubmed
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pubmed-article:19117487pubmed:articleTitleSkeletal and stereochemical diversification of tricyclic frameworks inspired by Ca(2+)-ATPase inhibitors, artemisinin and transtaganolide D.lld:pubmed
pubmed-article:19117487pubmed:affiliationDivision of Chemistry, Graduate School of Science, and Division of Innovative Research, Hokkaido University, N21, W10, Sapporo 001-0021, Japan.lld:pubmed
pubmed-article:19117487pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19117487pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed