PHOTOREACTION OF N-2-ALKENYLTHIOPHTHALIMIDES : 1,4-DITHIANE FORMATION BY INTRA- AND INTERMOLECULAR TWO-FOLD PHOTOREACTIONS AND THE X-RAY ANALYSIS OF THE DITHIANES

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概要

• 論文の詳細を見る

• Upon irradiation, N-2 alkenylthiophthalimides (8 and 9) effectively gave 1,4-dithianes as a pair of stereoisomers. The structures of the products, 10b-i and 10b-ii, are confirmed on the basis of their X-ray analyses. Plausible reaction pathways are discussed.

• 公益社団法人日本薬学会の論文
• 1986-10-25

著者

• 青江 啓一

  Organic Chemistry Research Laboratory, Tanabe Seiyaku Co., Ltd.,

• 佐藤 泰彦

  Organic Chemistry Research Laboratory, Tanabe Seiyaku Co., Ltd.,

• 金岡 祐一

  Faculty of Pharmaceutical Sciences, Hokkaido University

• 佐藤 泰彦

  Organic Chemistry Research Laboratory Tanabe Seiyaku Co. Ltd.

• 町田 實

  北海道医療大学歯学部

• 金岡 祐一

  Toyama Women's College

• 金岡 裕一

  Faculty Of Pharmaceutical Sciences Hokkaido University

• 町田 實

  Faculty of Pharmaceutical Sciences, Higashi Nippon Gakuen University

• 町田 實

  Faculty Of Pharmaceutical Sciences Higashi-nippon-gakuen University

• 小田 和明

  Faculty of Pharmaceutical Sciences, Higashi-Nippon-Gakuen University

• 青江 啓一

  Organic Chemistry Research Laboratory:tanabe Seiyaku Co. Ltd.

• 小田 和明

  北海道医療大学歯学部

• 小田 和明

  北海道医療大学薬学部薬化学教室

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