Skeletal and Stereochemical Diversification of Tricyclic Frameworks Inspired by Ca2+-ATPase Inhibitors, Artemisinin and Transtaganolide D.

[摘要]：with the three-dimensional structural diversity of tricyclic systems were designed and expeditiously synthesized (4-5 steps). A synthetic strategy featuring stereochem. diversification of ring-junctions and control of cyclization modes was devised to access varied mol. architectures in a systematic fashion.

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