[2,3]-Sigmatropic rearrangements of 3-sulfinyl dihydropyrans: application to the syntheses of the cores of ent-dysiherbaine and deoxymalayamicin A.

@article{FernndezdelaPradilla200823SigmatropicRO,
  title={[2,3]-Sigmatropic rearrangements of 3-sulfinyl dihydropyrans: application to the syntheses of the cores of ent-dysiherbaine and deoxymalayamicin A.},
  author={Roberto Fern{\'a}ndez de la Pradilla and Nadia Lwoff and Miguel A del {\'A}guila and Mariola Tortosa and Alma Viso},
  journal={The Journal of organic chemistry},
  year={2008},
  volume={73 22},
  pages={
          8929-41
        }
}
The [2,3]-sigmatropic rearrangement of a variety of configurationally stable diastereomeric allylic sulfinyl dihydropyrans, produced by base-promoted cyclization of sulfinyl dienols, has been studied. In some cases, the efficient transformation of these substrates into dihydropyranols required an in-depth study of reaction conditions, with the preferred protocol relying on the use of DABCO in warm toluene. This methodology has been applied to the syntheses of the cores of ent-dysiherbaine and… 
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