Synthesis of Oxazolidin-2-ones and Imidazolidin-2-ones Directly from 1,3-Diols or 3-Amino Alcohols using Iodobenzene Dichloride and Sodium Azide

被引：11
|
作者：
He, Tian [1 ]
Gao, Wen-Chao [1 ]
Wang, Wei-Kun [1 ]
Zhang, Chi [1 ]
机构：
[1] Nankai Univ, State Key Lab Elementoorgan Chem, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Res Inst Elementoorgan Chem, Tianjin 300071, Peoples R China
来源：
ADVANCED SYNTHESIS & CATALYSIS | 2014年 / 356卷 / 05期
基金：
中国国家自然科学基金;
关键词：
imidazolidin-2-ones; iodobenzene dichloride; oxazolidin-2-ones; sodium azide; CATALYTIC OXIDATIVE CARBONYLATION; ONE-POT SYNTHESIS; CYCLIC UREAS; CARBON-DIOXIDE; STEREOSELECTIVE SYNTHESIS; FACILE SYNTHESIS; 2-OXAZOLIDINONES; OXAZOLIDINONES; CONVERSION; OPTIMIZATION;
D O I：
10.1002/adsc.201300982
中图分类号：
O69 [应用化学];
学科分类号：
081704 ;
摘要：
A general and efficient method for the synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols and 3-amino alcohols has been developed using the same reagent combination of iodobenzene dichloride (PhICl2) and sodium azide (NaN3).
引用
收藏
页码：1113 / 1118
页数：6
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