Sequential [3+2] cycloaddition/reaffangement reaction of imidazolone nitrones and allenoates for the efficient synthesis of functionalized imidazolidinone

被引：32
|
作者：
Wu, Xi [1 ]
Na, Risong [1 ]
Liu, Honglei [1 ]
Liu, Jun [1 ,2 ]
Wang, Min [1 ]
Zhong, Jiangchun [1 ]
Guo, Hongchao [1 ]
机构：
[1] China Agr Univ, Dept Appl Chem, Beijing 100193, Peoples R China
[2] Chem Ind Press, Beijing 100011, Peoples R China
来源：
TETRAHEDRON LETTERS | 2012年 / 53卷 / 03期
基金：
中国国家自然科学基金;
关键词：
Cycloaddition; Rearrangement; Sequential reaction; Nitrone; Allenoate; CHIRAL NITRONES; 1,3-DIPOLAR CYCLOADDITION; DIPOLAR CYCLOADDITION; ALLENES; PRECURSORS;
D O I：
10.1016/j.tetlet.2011.11.049
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Sequential [3+2] cycloaddition/rearrangement reaction of imidazolone nitrones and allenoates is described. The reaction was carried out in refluxing toluene to provide the methylene imidazolidinone derivatives in high yield. It provides a simple and convenient strategy for the synthesis of functionalized imidazolidinones. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码：342 / 344
页数：3
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