Stereoselective oxylactonization. Preparation of 2-deoxy-DL-ribono-1,4-lactone derivatives from 3-silyloxy-4-alkenamides.

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概要

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• The oxylactonization of 3-silyloxy-4-alkenamides proceeds stereoselectively by treatment with <I>m</I>-chloroperbenzoic acid to give the corresponding 2-deoxy-DL-ribono-1,4-lactone derivatives.

• 公益社団法人 日本化学会の論文

著者

• Miwa Tetsuo

  Department of Chemistry, Faculty of Science, The University of Tokyo

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• Stereoselective oxylactonization. Preparation of 2-deoxy-DL-ribono-1,4-lactone derivatives from 3-silyloxy-4-alkenamides.

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