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

Osamu Kitagawa; Katsuyuki Aoki; Tadashi Inoue; Takeo Taguchi

doi:10.1016/0040-4039(94)02261-9

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 › 査読

23 被引用数 (Scopus)

抄録

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.

本文言語	English
ページ（範囲）	593-596
ページ数	4
ジャーナル	Tetrahedron Letters
巻	36
号	4
DOI	https://doi.org/10.1016/0040-4039(94)02261-9
出版ステータス	Published - 1995 1月 23
外部発表	はい

ASJC Scopus subject areas

生化学
創薬
有機化学

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10.1016/0040-4039(94)02261-9

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AU - Taguchi, Takeo

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

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