Abstract
The reaction of Viehe's salt (Me2N+=CCl2Cl-) with various carbohydrate diols (manno, allo) in the presence of a base is reported, the products being, after hydrolysis, either carbonate (with pyridine) or the carbamate (with triethylamine). A rationalization of the two different types of product formed is given in terms of the stereoelectronic control proposal by Deslongchamps.

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