USING MICROBIAL REDUCTION TO SYNTHESIZE CARBACYCLIN

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概要

• 論文の詳細を見る

• Microbial reduction of 7-methoxycarbonyl bicyclo[4. 3. 0]non-3-en-8-one ((±)-3) afforded the optically active (-)-3,which was efficiently converted by ring contraction using thallium (III) nitrate to the intermediate (11) used to synthesize carbacyclin (1).

• 公益社団法人日本薬学会の論文
• 1986-07-25

著者

• 末宗 洋

  Faculty of Pharmaceutical Sciences, Kyushu University

• 酒井 浄

  Faculty of Pharmaceutical Sciences, Kyushu University

• 酒井 浄

  Faculty Of Pharmaceutical Sciences Kyushu University

• 末宗 洋

  九州大学薬学部

• 秋田 弘幸

  School Of Pharmaceutical Science Toho University

• 秋田 弘幸

  理化学研究所

• 大石 武

  The Institute of Physical and Chemical Research (Riken)

• 末宗 洋

  九州大学大学院薬学府

• 船越 和久

  Faculty Of Pharmaceutical Sciences Kyushu University

• 秋田 弘幸

  The Institute of Physical and Chemical Research (Riken)

• Xie Zhuo-Feng

  Faculty of Pharmaceutical Sciences, Kyushu University

• Xie Z‐f

  Kyushu Univ. Fukuoka Jpn

• Xie Zhuo-feng

  Faculty Of Pharmaceutical Sciences Kyushu University

• 末宗 洋

  九州大学大学院薬学研究院

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