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

来源：

ASIAN JOURNAL OF CHEMISTRY | 2013年 / 25卷 / 03期

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

页码：1558 / 1560

页数：3

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