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Formal synthesis of ent-dysiherbaine from sulfinyl dihydropyrans by sigmatropic rearrangement and tethered aminohydroxylation
Authors:Roberto Ferná  ndez de la Pradilla,Nadia Lwoff,Alma Viso
Affiliation:Instituto de Química Orgánica, CSIC, Juan de la Cierva, 3, 28006 Madrid, Spain
Abstract:A stereospecific [2,3]-sigmatropic rearrangement of a sulfinyl dihydropyran, followed by a tethered aminohydroxylation reaction, are the key steps of a formal synthesis of ent-dysiherbaine from an enantiopure sulfinyl dienol.
Keywords:Allylic sulfoxides   Sigmatropic rearrangement   Tethered aminohydroxylation
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