The Reduction of Chlorodeoxy Sugars by Tributyltin Hydride

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概要

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• Acetylated chlorodeoxy sugars were prepared by the use of sulfuryl chloride. These chlorodeoxy sugars were then successfully reduced to deoxy sugars by the use of tri-<I>n</I>-butyltin hydride. α,α-Azobis-isobutyronitrile, which has been known to be an effective radical initiator, was found to be indispensable for the reaction.

• 公益社団法人 日本化学会の論文

著者

• Ueda Nobuhiko

  Department of Chemistry, Osaka University College of Science

• Arita Hitoshi

  Department of Chemistry, Osaka University College of Science

関連論文

• Treatment Parameters for the Efficacy of Transscleral Cyclophotocoagulation in Rabbits Using a Diode Laser
• The Reduction of Chlorodeoxy Sugars by Tributyltin Hydride

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