Iodocarbocyclization and iodoaminocyclization reactions mediated by a metallic reagent

Osamu Kitagawa, Takeo Taguchi

研究成果: Article査読

63 被引用数 (Scopus)

抄録

We have developed new iodine-mediated carbocyclization and aminocyclization reactions through activation of intramolecular carbon or amide nucleophiles by metallic reagents. In the presence of 12 and Ti(OR)4 or TiCl4-Et3N, iodocarbocyclization of various active methine compounds having alkenyl or alkynyl groups proceeded in a highly stereospecific manner to give iodocyclo-alkanes or -alkenes in good yields. The present reaction can be also applied to asymmetric catalytic reaction; that is, the reaction of 4-alkenylmalonate derivatives with Ti(TADDOLate)2 catalyst gave iodoalkylcyclopentanes with excellent enantioselectivity (> 95%ee). Furthermore, iodoaminocyclization of unsaturated amide derivatives with an ambident nucleophilic center and iodoaziridination of N-allylic tosylamides, featuring regiocontrol and an activation of an amide nucleophile by a basic metallic reagent, were also established.

本文言語English
ページ(範囲)1191-1199
ページ数9
ジャーナルSynlett
8
DOI
出版ステータスPublished - 1999 1 1
外部発表はい

ASJC Scopus subject areas

  • 有機化学

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