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Chiral pyrylium salts are almost unknown in the literature, and none that are epimerizable have been reported prior to our work. Herein, we report two new epimerizable pyryliums and the kinetics of the diastereomeric equilibration of these and one other example. All of these required a careful analysis of the (1)H NMR spectrum to identify the stereoisomers, particularly for one of them. The temporal evolution of the relative isomeric concentrations was determined through acquisition of progressive NMR spectra. The base-catalyzed isomerization kinetics were successfully modeled as sequential, pseudo-first-order reactions that transition through a long-lived intermediate. These results suggest that the pseudobase intermediate is the operative catalyst when epimerizations are initiated with amines with pK(a) 7.4 or greater. Given the bulky nature of the operative acid (pyrylium) and base (pseudobase), the rate of these epimerizations is sensitive to steric bulk in the pyrylium. Thus, the reaction kinetics slow by a factor of 25 when substituents are placed at the ortho versus para position on the pyrylium cyclohexane ring. This is likely due to the difficulty of pseudobase attack at the sterically crowded pyrylium acidic hydrogen position.

Synthesis of New Chiral Pyrylium Salts and Their Phosphinine and Pyridine Derivatives. -Reactions of ketone (I) with acyl chlorides provide new chiral and achiral pyrylium salts. Treatment of the latter with tris(trimethylsilyl)phosphine or ammonium hydroxide results in the formation of phosphinine and pyridine derivatives. -(VAN DER VELDE, N. A.; KORBITZ, H. T.; GARNER*, C. M.; Tetrahedron Lett. 53 (2012) 43, 5742-5744, http://dx.

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