Pseudo Three-Component Synthesis of 1,3-Dioxol Derivatives from the Reaction Between Isocyanides and Aldehydes in Solventless Conditions

被引:0
|
作者
Kazemizadeh, Ali Reza [1 ]
Ramazani, Ali [1 ]
机构
[1] Islamic Azad Univ, Zanjan Branch, Dept Chem, Res Lab MCRs, Zanjan, Iran
关键词
Isocyanide; Multicomponent reactions; 1,3-Dioxol derivatives; Solventless conditions; STABILIZED PHOSPHORUS YLIDES; ONE-POT SYNTHESIS; 2,2-DISUBSTITUTED INDANE-1,3-DIONE DERIVATIVES; PASSERINI MULTICOMPONENT REACTION; STEREOSELECTIVE-SYNTHESIS; ACETYLENIC ESTERS; ALKYL; ACID; INDANE-1,2,3-TRIONE; DIALKYL;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pseudo three-component reaction between isocyanides and aldehydes in a 1:2 ratio in solventless conditions at room temperature led to 1,3-dioxol derivatives in high yields. The reaction proceeds cleanly under mild conditions and no side reactions were observed. The structures of the products were deduced from their H-1 NMR, C-13 NMR, mass, IR spectra and elemental analysis.
引用
收藏
页码:1558 / 1560
页数:3
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