Acyclic C-nucleoside analogs of the type of 5-C-polyhydroxyalkyl-1,3,4-thiadiazoles.

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概要

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• The synthesis of some acyclic <I>C</I>-nucleoside analogs possessing thiadiazole rings was achieved by the heterocyclization of the 4-arylthiosemicarbazones of D-galactose, D-glucose, D-mannose, D-arabinose, and lactose, Acetylation of the thiadiazoles afforded the corresponding 2-(<I>N</I>-acetylarylamino)-5-polyacetoxyalkyl-1,3,4-thiadiazoles and periodate oxidation gave the corresponding 5-(arylamino)-1,3,4-thiadiazole-2-carbaldehyde.

• 公益社団法人 日本化学会の論文

著者

• Mousaad Ahmed

  Chemistry Department, Faculty of Science, Alexandria University

• El Ashry

  Chemistry Department, Faculty of Science, Alexandria University

• Nassr Mahmoud

  Chemistry Department, Faculty of Science, Alexandria University

• El Kilany

  Chemistry Department, Faculty of Science, Alexandria University

関連論文

• Acyclic C-nucleoside analogs of the type of 5-C-polyhydroxyalkyl-1,3,4-thiadiazoles.

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