Absolute Stereochemistry of (-)-Preorixine and Related Compounds

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概要

• 論文の詳細を見る

• The absolute stereochemistry of the C-2' position of (-)-preorixine, postulated to be an important biosynthetic precursor of various quinoline alkaloids, was assigned as R by the combination of its chemical transformation and the extended Mosher method. The stereochemistry of the C-2' position of (+)-orixine was also concluded to be R, establishing taht no inversion occurred when (-)-preorixine was transformed into (+)-orixine.

• 公益社団法人日本薬学会の論文
• 1996-10-15

著者

• 野副 重男

  東北大薬

• Murata K

  Faculty Of Pharmaceutical Sciences Tohoku University

• FUNAYAMA Shinji

  Department of Kampo Pharmaceutical Sciences, Nihon Pharmaceutical University

• Murata Kiyoshi

  Faculty Of Pharmaceutical Sciences Tohoku University

• NOZOE Shigeo

  Faculty of Pharmaceutical Sciences, Tohoku University

• Murata K

  Graduate School Of Pharmaceutical Sciences Osaka University

• Nozoe Shigeo

  Faculty Of Pharmaceutical Sciences Tohoku University

• FUNAYAMA Shinji

  (Present address)Dept. of Bioscience and Biotechnology, Aomori University

• Funayama S

  Dep. Of Kampo Pharmaceutical Sciences Nihon Pharmaceutical Univ.

• Nozoe Shigeo

  Faculty Of Pharmaceutical Science Tohoku University

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