Conformational Difference between Mono- and Diprotonated cis-2,5-Diphenylpiperazinium Salts in the Solid State

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概要

• 論文の詳細を見る

• Monohydrochlorides of cis-2,5-diphenylpiperazine assume a chair conformation, while the corresponding dihydrochlorides assume a boat form regardless of the substituent(s) at the nitrogen atom.

• 公益社団法人日本薬学会の論文
• 2000-12-01

著者

• 高須 清誠

  京都大学大学院薬学研究科

• 冨士 薫

  Institute For Chemical Research Kyoto University

• Takasu Kiyosei

  Institute Of Chemical Research Kyoto University

• TAGA Tohru

  Faculty of Pharmaceutical Sciences, Kyoto University

• Taga Tohru

  Faculty Of Pharmaceutical Sciences Kyoto University

• Bando Masahiko

  Otsuka Parmaceutical Co. Ltd.

• Taga T

  Faculty Of Pharmaceutical Sciences Kyoto University

• TAKASU Kiyosei

  Instutite for Chemical Research, Kyoto University

• MIYAMOTO Hisashi

  Otsuka Pharmaceutical Co., Ltd.,

• TANAKA Kiyoshi

  Instutite for Chemical Research, Kyoto University

• FUJI Kaoru

  Instutite for Chemical Research, Kyoto University

• Miyamoto Hisashi

  Otsuka Pharmaceutical Co. Ltd.

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