EFFECTS OF SUBSTITUENTS ON THE CHLORINATION OF METHYL 3-HYDROXYTHIOPHENE-2-CARBOXYLATE AND ON THE REACTION OF THE RESULTING CHLORINATED PRODUCTS WITH ACTIVE HYDROGEN CONTAINING COMPOUNDS

被引：9

作者：

CORRAL, C

LISSAVETZKY, J

MANZANARES, I

机构：

[1] Institute, de Química Médica, CSIC, Madrid, 28006

来源：

JOURNAL OF HETEROCYCLIC CHEMISTRY | 1990年 / 27卷 / 02期

关键词：

D O I：

10.1002/jhet.5570270237

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The title tandem reactions that produce 5‐substituted compounds of methyl 3‐hydroxythiophene‐2‐carboxylate can also be applied with a minor modification to the 4‐alkyl and 4‐aryl derivatives thereof. On the other hand, 5‐alkyl and 5‐aryl derivatives that undergo a similar smooth chlorination behave in the second reaction in a different manner. Copyright © 1990 Journal of Heterocyclic Chemistry

引用

页码：315 / 319

页数：5

共 10 条

[1]

BIEVER P, 1954, ANN CHIM, V9, P674

[2]

BRELIVET J, 1971, B SOC CHIM FR, P1344

[3] REACTIONS WITH METHYL 3-HYDROXYTHIOPHENE-2-CARBOXYLATE .2. A NEW ROUTE TO MONO-ALKYL AND DI-ALKYL ETHERS OF THIOTETRONIC AND ALPHA-HALOGENOTHIOTETRONIC ACIDS [J].