This invention relates to a process for stereoselectively preparing a nucleoside of the following formula: wherein R.sub.3, R.sub.4, and B are defined herein. The process includes reacting a furanose compound with a nucleobase in the presence of a halide salt. Also disclosed is another process for stereoselectively synthesizing an intermediate that can be used to make the starting compound in the first-mentioned process.

 
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> Method of preparing percarboxy-cyclodextrins by means of regioselective oxidation at position 6 of alpha-, beta-, or gamma- cyclodextrins and applications thereof

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