电邮这篇文章 New Method of Synthesis of Biologically Active Get(aryl)chalcogenylacetates of Tris(2-hydroxyethyl)ammonium
- 作者: Adamovich S.N.1, Oborina Е.N.1, Ushakov I.А.2, Mirskova А.N.1
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隶属关系:
- A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- Irkutsk National Research Technical University
- 期: 卷 88, 编号 10 (2018)
- 页面: 2227-2229
- 栏目: Letters to the Editor
- URL: https://journal-vniispk.ru/1070-3632/article/view/222512
- DOI: https://doi.org/10.1134/S1070363218100353
- ID: 222512
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详细
Physiologically and pharmacologically active het(aryl)chalcogenylacetates of tris(2-hydroxyethyl)ammonium of pharmacopeial purity have been synthesized by the reaction of het(aryl)chalcogenylacetic acids with sodium (potassium) hydroxide and triethanolamine hydrochloride by one-pot method in quantitative yield (up to 99.8%).
作者简介
S. Adamovich
A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
编辑信件的主要联系方式.
Email: mir@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033
Е. Oborina
A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: mir@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033
I. Ushakov
Irkutsk National Research Technical University
Email: mir@irioch.irk.ru
俄罗斯联邦, Irkutsk
А. Mirskova
A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: mir@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033
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