Free-Radical Mediated [3 + 2] Methylenecyclopentane Annulations of Electron-Poor Alkenes

Abstract
Methylenecyclopropanes that on ring opening form unstabilized or electron-rich radicals effect methylenecyclopentane annulations of electron-poor alkenes in good yields with thiyl-radical catalysis. Similar vinylcyclopropane-based annulations involving unstabilized radicals can also succeed under stannyl-radical catalysis.
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