Synthesis of 14β-Pregnanes. II. Nuclear Magnetic Resonance Sepctroscopic Evidence for the Conformation of the C-Rings in C/D cis-11β, 12β-Oxygenated Pregnanes

• 三橋 博

• 福岡 正道

抄録

The synthesis of C/D cis 11β, 12β-oxygenated pregnane derivatives from 3β, 12β-diacetoxy-5α, 25D-spirostan-11-one (II) vis dienone (V) is described. Nuclear magnetic resonance studies indicated the possible conformation of the C-ring in C/D-cis pregnane is not a boat but a chair form.

収録刊行物

• ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ

  ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ 17 (2), 324-328, 1969

  公益社団法人 日本薬学会

キーワード

• Drug Discovery
• General Chemistry
• General Medicine

詳細情報

• CRID: 1390282679149954304
• NII論文ID: 110003620883
• NII書誌ID: AA00602100
• DOI: 10.1248/cpb.17.324
• ISSN: 13475223
• ISSN: 00092363
• Web Site: http://www.jstage.jst.go.jp/article/cpb1958/17/2/17_2_324/_pdf
• Web Site: https://search.jamas.or.jp/link/ui/1970106501
• 本文言語コード: en
• データソース種別:
  • JaLC
  • Crossref
  • CiNii Articles
• 抄録ライセンスフラグ: 使用不可