Abstract
The reaction of l-methylene-2-trimethylsilyl spiro[2.n] alkanes with aldehydes under almost neutral conditions using tetrabutylammonium fluoride is consistent with 80% of diastereoisomeric pairs of spiromethylene cyclopropyl carbinols. This study elucidates the stereochemistry of these alcohols using the GC/FT-IR technique for inseparable mixtures and FT-IR dilution technique for a separable pair.
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