An N 3-(p-methoxyphenoxy)acetyloxazolidine-2-thione has been synthesized and employed in the glycolate asymmetric aldol addition reaction with aromatic and aliphatic aldehydes. The observed diastereoselectivies ranged from 62:38 to 80:20 when the reaction was conducted at-25 o C. The diastereoselectivities improved to 75:25 to 94:6 when the reaction was conducted at-78 o C. The absolute stereochemistry of the aldol adducts was determined by 1 H NMR spectroscopy and X-ray crystallography. The 1 H NMR spectra of the aldol adducts contained a signal (the -proton of the glycolate position of the aldol sidechain) that was highly deshielded.

A new synthetic methodology has been developed for the synthesis of sulfinate alkyl and aryl esters. The methodology involves the combination of <i>p</i>-toluenesulfinic acid and 1,1’-carbonyl diimidazole (CDI) to create the putative reagent sulfinyl imidazole. The process spontaneously releases carbon dioxide upon the addition of the CDI to the acid suggesting the rapid formation of the proposed reagent. Reaction of this reagent with a series of alcohols (primary, secondary, and tertiary) afforded the corresponding sulfinate alkyl esters in good to excellent yield by the addition of alcohols. It was also possible to form the related sulfinate aryl esters by treating the proposed sulfinyl imidazole with selected phenols (phenol, <i>p</i>-tert-butylphenol, and thymol). The aryl esters were formed in excellent conversion based on analysis of the 500 MHz 1H NMR spectra of the crude reaction mixtures.

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