Browsing by Subject "c-aryl glycosides"
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Item Synthetic studies on the pluramycin family of antitumor antibiotics : the total synthesis of isokidamycin(2010-12) O'Keefe, Brian Michael; Martin, Stephen F.; Krische, Michael J.; Bielawski, Christopher W.; Laude, David A.; Whitman, Christian P.A total synthesis of the complex C-aryl glycoside isokidamycin was achieved during an effort to construct the natural product kidamycin, a member of the pluramycin family of antitumor antibiotics. The angolosamine carbohydrate was appended, along with annelation of a benzene ring by the implementation of the Martin group's silicon tether-directed, intramolecular aryne-furan cycloaddition strategy. The vancosamine-derived carbohydrate was then installed by an O -> C-glycoside rearrangement. A novel protocol for the carbonylative cross-coupling of ortho-disubstituted aryl iodides with aryl boronic acids and alkynyl zinc reagents was also discovered during efforts to introduce the pyranone ring of kidamycin. The reaction proved general, as a variety of electron-rich and electron-poor aryl iodides, boronic acids, and alkynyl-zinc reagents participated in the cross-coupling.