Abstract
6,6- and 6,5-Spiroketals were prepared in good overall yields by alkylation and epoxide-opening reactions of 3,4-dihydro-6-[( para-toluenesulfonyl)methyl]-2 H-pyran ( 1) and subsequent acid catalysed cyclisation. The diastereoselectivity of the cyclisations was determined by a combination of 2D-NMR spectroscopy and X-ray crystallography. Attempted preparation of a 7,6-spiroketal using the same methodology was unsuccessful.
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