Synthetic Route to 2-Deoxyaldoses by Fluoride-Catalyzed Solvolysis of Enol-Phosphate Esters

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概要

• 論文の詳細を見る

• 1-Alkenyl and phenyl phosphate esters undergo smooth cleavage of the phosphorus-oxygen linkage by fluoride-catalyzed alcoholysis to give aldehydes (ketones) and phenols, respectively. Application of this method provides a new route to 2-deoxyaldosugars from the enol-phosphates derived from vinylene carbonate telomers.

• 社団法人日本薬学会の論文
• 1980-04-25

著者

• 三尾 直樹

  Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)school Of Pharmacy Tokushima

• 滝沢 武夫

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 国枝 武久

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 滝沢 武夫

  Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address) Department Of Chemistry Uni

• 阿部 芳廣

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 国枝 武久

  Faculty Of Pharmaceutical Sciences Kumamoto University

• 国枝 武久

  Faculty Of Pharmaceutical Sciences University Of Tokyo

関連論文

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