Chemistry–A European Journal

An Efficient, Overall [4+ 1] Cycloadditon of 1, 3??Dienes and Nitrene Precursors

Q Wu, J Hu, X Ren, JS Zhou

Index: Wu, Qiong; Hu, Jian; Ren, Xinfeng; Zhou, Jianrong Chemistry - A European Journal, 2011 , vol. 17, # 41 p. 11553 - 11558

Full Text: HTML

Citation Number: 23

Abstract

Abstract Intermolecular cycloadditions of conjugated dienes and nitrene precursors usually produce aziridines. A generally useful method was lacking to directly provide the [4+ 1] cycloadducts, 3-pyrrolines. We have realized this transformation by using an uniquely active catalyst, copper (II) 1, 1, 1, 5, 5, 5-hexafluoroacetylacetonate ([Cu (hfacac) 2]). The method is applicable to a wide array of dienes with good yields. When 1, 4-disubsituted dienes are ...

Related Articles:

Reaction of perhalofluoroalkyl sulfinates with one-electron transfer oxidants. A facile method for the synthesis of perhalofluorocarboxylic acids

[Journal of Fluorine Chemistry, , vol. 49, # 3 p. 433 - 437]

High Temperature, Vapor Phase Reactions of Some Fluorocarbon Derivatives with Oxidizing Agents

[Journal of the American Chemical Society, , vol. 80, p. 2313,2316]

Reaction of perhalofluoroalkyl sulfinates with one-electron transfer oxidants. A facile method for the synthesis of perhalofluorocarboxylic acids

[Journal of Fluorine Chemistry, , vol. 49, # 3 p. 433 - 437]

Chlorotrifluoroethylene-derived fluids. I. Model compound synthesis

[Journal of Fluorine Chemistry, , vol. 55, # 3 p. 271 - 282]

5-Perfluoroalkyl bicyclic amide acetals

[Journal of Fluorine Chemistry, , vol. 21, p. 359 - 364]

More Articles...