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

• TAKASU Kiyosei

• MIYAMOTO Hisashi

• TANAKA Kiyoshi

• TAGA Tohru

• BANDO Masahiko

• FUJI Kaoru

抄録

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.

収録刊行物

• ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ

  ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ 48 (12), 2014-2016, 2000

  公益社団法人 日本薬学会

キーワード

• piperazine
• conformation
• X-ray analysis
• ^<15>N-NMR

詳細情報

• CRID: 1390001204160586112
• NII論文ID: 130003948009
• NII論文ID: 110003635421
• NII書誌ID: AA00602100
• DOI: 10.1248/cpb.48.2014
• COI: 1:CAS:528:DC%2BD3cXos1eitLw%3D
• ISSN: 13475223
• ISSN: 00092363
• ISSN: http://id.crossref.org/issn/00092363
• NDL書誌ID: 5584975
• PubMed: 11145163
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I5584975
• Web Site: http://www.jstage.jst.go.jp/article/cpb1958/48/12/48_12_2014/_pdf
• 本文言語コード: en
• データソース種別:
  • JaLC
  • NDL
  • Crossref
  • PubMed
  • CiNii Articles
• 抄録ライセンスフラグ: 使用不可