Synlett 1998; 1998(12): 1402-1404
DOI: 10.1055/s-1998-1967
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Carbohydrates to Carbocycles: Regio- and Stereoselectivity in the Intramolecular [2+2] Photocycloaddition of Dienic 2-Enono-δ-lactones

Ana M. Gómez* , Susana Mantecón, Sara Velazquez, Serafín Valverde, Pal Herczegh, J. Cristóbal López
  • *Instituto de Química Orgánica General, C.S.I.C., Juan de la Cierva 3, Madrid 28006, Spain; Fax 34 91 5 64 48 53; E-mail: clopez@cc.csic.es
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Carbohydrate derived 2-enono-δ-lactones, substituted at C-6, C-7 or C-8 with an electron-rich unsaturation, undergo efficient [2+2] intramolecular photocycloaddition to generate densely functionalized, fused carbocyclic systems.

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