Functionally Substituted Isothiazole- and Isoxazolecarboxamides
- 作者: Dikusar E.A.1, Petkevich S.K.1, Zhukovskaya N.A.1, Zvereva T.D.1, Kurman P.V.2
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隶属关系:
- Institute of Physical Organic Chemistry
- Institute of Bioorganic Chemistry
- 期: 卷 55, 编号 4 (2019)
- 页面: 462-468
- 栏目: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/220249
- DOI: https://doi.org/10.1134/S1070428019040079
- ID: 220249
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详细
Convenient synthetic approaches to functionally substituted 5-phenyl-1,2-oxazole-3-carboxamides and 4,5-dichloro-1,2-thiazole-3-carboxamides were developed on the basis of reactions of the corresponding carboxylic acid chlorides with primary aromatic and aliphatic amines. Optimal ratios acid chloride—amine (or amine hydrochloride)–triethylamine were found so that the reaction did not involve active chlorine atom in position 5 of the isothiazole ring.
作者简介
E. Dikusar
Institute of Physical Organic Chemistry
编辑信件的主要联系方式.
Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk
S. Petkevich
Institute of Physical Organic Chemistry
Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk
N. Zhukovskaya
Institute of Physical Organic Chemistry
Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk
T. Zvereva
Institute of Physical Organic Chemistry
Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk
P. Kurman
Institute of Bioorganic Chemistry
Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk
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