Reaction between alkyl isocyanides and dialkyl acetylenedicarboxylates in the presence of 1-aryl-2-thiocyanatoethanone yields highly functionalised iminolactones

被引：3

作者：

Hassanabadi, Alireza ^{[1
]}

Hosseini-Tabatabaei, Mohammad R. ^{[1
]}

机构：

[1] Islamic Azad Univ, Zahedan Branch, Dept Chem, Zahedan, Iran

来源：

JOURNAL OF CHEMICAL RESEARCH | 2012年 / 12期

关键词：

three-component reactions; dialkyl acetylenedicarboxylates; alkyl isocyanides; 1-aryl-2-thiocyanatoethanone; ONE-POT SYNTHESIS; DIMETHYL ACETYLENEDICARBOXYLATE; HETEROCYCLIC-SYSTEMS; ACETYLENIC ESTERS; CONSTRUCTION; CONDENSATION; DERIVATIVES; ANHYDRIDE;

D O I：

10.3184/174751912X13518651809556

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The reactive intermediate produced in the reaction between alkyl isocyanides and dialkyl acetylenedicarboxylates was trapped by 1-aryl-2-thiocyanatoethanone to yield highly functionalised iminolactones derivatives in good yields.

引用

页码：706 / 708

页数：3

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