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

页码：1113 / 1118

页数：6

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