Regiocontrolled Iodoaminocyclization Reaction of an Ambident Nucleophile Mediated by Basic Metallic Reagent

Masao Fujita, Osamu Kitagawa, Takashi Suzuki, Takeo Taguchi

研究成果: Article

54 引用 (Scopus)

抜粋

A new and general method of iodine-mediated cyclization reactions of allyl or homoallyl carbamates, ureas, and amides was found to give N-cyclized products as single regioisomers. The present reaction proceeded in good yield through regiocontrol (N-cyclization > O-cyclization) and the increase in the reactivity of an ambident nucleophile by a basic metallic reagent. The N-cyclization selectivity was remarkably affected by the additive employed. The iodoaminocyclization reaction of the homoallyl carbamates and ureas with a chiral center at the homoallylic position was found to proceed with high 1,3-cis- and 1,3-trans-selectivity, respectively.

元の言語English
ページ(範囲)7330-7335
ページ数6
ジャーナルJournal of Organic Chemistry
62
発行部数21
DOI
出版物ステータスPublished - 1997 1 1

    フィンガープリント

ASJC Scopus subject areas

  • Organic Chemistry

これを引用