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Synlett 1994; 1994(4): 273-274
DOI: 10.1055/s-1994-22825
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Free-Radical Mediated [3 + 2] Methylenecyclopentane Annulations of Electron-Poor Alkenes

C. C. Huval* , K. M. Church, D. A. Singleton
  • *Department of Chemistry, Texas A&M University, College Station, Texas 77843-3255 USA
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Publikationsdatum:
22. März 2002 (online)

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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.