Abstract
The preferential conformer and conformer ratio in the cyclohexane, oxane, and thiane derivatives bearing both trimethylsiloxy (or methoxymethyleneoxy) and tributylstannyl groups at the geminal position were determined on the basis of their 3 J( 1 1 9 Sn- 1 3 C) coupling constants and 1 3 C NMR spectral analyses at low temperature.
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