Diels-Alder reaction of N-allylic enamides and lactam derivatives through iodine mediated activation

Osamu Kitagawa, Katsuyuki Aoki, Tadashi Inoue, Takeo Taguchi

研究成果: Article

23 引用 (Scopus)

抜粋

The Diels-Alder reaction of N-allylic enamide and α,β-unsaturated lactam derivatives proceeded in the presence of I2 at low temperature through a cationic iodolactonization intermediate. With some substrates, this method of activation was proved to be more effective than by use of Lewis acids.

元の言語English
ページ(範囲)593-596
ページ数4
ジャーナルTetrahedron Letters
36
発行部数4
DOI
出版物ステータスPublished - 1995 1 23
外部発表Yes

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ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

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