SYNTHETIC STUDIES ON N-ACETYL DERIVATIVES OF AMINO-ACIDS AND THIOLACTONE USING VILSMEIER-HAACK REAGENT

被引：29

作者：

BALASUNDARAM, B ^{[1
]}

VENUGOPAL, M ^{[1
]}

PERUMAL, PT ^{[1
]}

机构：

[1] CENT LEATHER RES INST,DIV ORGAN CHEM,MADRAS 600020,TAMIL NADU,INDIA

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 26期

关键词：

D O I：

10.1016/S0040-4039(00)60540-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A variety of N-acetyl derivatives of amino acids have been subjected to Vilsmeier reagent to obtain 2,4-dichloro-3,5-diformylpyrrole and 2-formylmethylene-4-substituted oxazolidin-5-ones. The N-acetyl homo cysteine thiolactone gave 5-chloro-3-formylthieno (2,3-b)pyridine on reaction with Vilsmeier reagent.

引用

页码：4249 / 4252

页数：4

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