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Synthesis of enantiopure ethyl deoxymonate B from allylic sulfinyl dihydropyrans
Authors:Roberto Fernández de la Pradilla  Nadia Lwoff
Institution:Instituto de Química Orgánica, CSIC, Juan de la Cierva, 3, 28006 Madrid, Spain
Abstract:A completely stereoselective dihydroxylation of a dihydropyranol and a cross-metathesis in the presence of a free homoallylic hydroxyl group are the key steps of a synthesis of enantiopure ethyl deoxymonate B from a sulfinyl dienol.
Keywords:Pseudomonic Acids  Allylic Sulfoxides  Sigmatropic rearrangement  Stereoselective dihydroxylation
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