Photocyclization of styrylpyrazines.

• 太田 明廣

• 長谷川 和子

• 天野 克代

• 森 千春

• 大沢 明子

• 池田 清貴

• 渡辺 徳弘

抄録

Irradiation of several 2-(β-arylvinyl) pyrazines at room temperature using a high pressure mercury lamp afforded aza-phenanthrenes in moderate yields. The ring closure of 2-[β-(3-pyridyl) vinyl] pyrazine (IIIb) occurred only at the 4-position of the pyridine ring, whereas 2-[β-(2-naphthyl) vinyl] pyrazine (IIIe) cyclized at the 1-position of the naphthalene ring. 2, 5-Distyrylpyrazine (VIa) and 2, 5-bis [β-(2-pyridyl) vinyl] pyrazine (VIb) were also irradiated in refluxing benzene to give dibenzo [a, h] phenazine (XVI) and dipyrido [3, 2-α : 3´, 2´-h] phenazine (XVII), respectively.

収録刊行物

• ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ

  ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ 27 (11), 2596-2601, 1979

  公益社団法人 日本薬学会

キーワード

• polycyclic phenazine derivatives

詳細情報

• CRID: 1390001204165239936
• NII論文ID: 110003623506
• NII書誌ID: AA00602100
• DOI: 10.1248/cpb.27.2596
• ISSN: 13475223
• ISSN: 00092363
• Web Site: http://www.jstage.jst.go.jp/article/cpb1958/27/11/27_11_2596/_pdf
• Web Site: https://search.jamas.or.jp/link/ui/1980110481
• 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