Tetrahedron Letters p. 3425 - 3428 (1991)
Update date:2022-08-03
Topics:
Sansbury, Francis H.
Warren, Stuart
Acid-catalysed cyclisation of substituted 1,6- or 1,4-alkane diols with suitably placed phenylthio groups leads to high yields of tetrahydropyrans formed by exo or endo hydroxyl participation during phenylthio migration with inversion at both the migration origin and terminus.
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