Enviar artigo por via de e-mail New Method of Synthesis of Biologically Active Get(aryl)chalcogenylacetates of Tris(2-hydroxyethyl)ammonium
- Autores: Adamovich S.1, Oborina Е.1, Ushakov I.2, Mirskova А.1
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Afiliações:
- A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- Irkutsk National Research Technical University
- Edição: Volume 88, Nº 10 (2018)
- Páginas: 2227-2229
- Seção: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/222512
- DOI: https://doi.org/10.1134/S1070363218100353
- ID: 222512
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Resumo
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%).
Sobre autores
S. Adamovich
A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Autor responsável pela correspondência
Email: mir@irioch.irk.ru
Rússia, ul. Favorskogo 1, Irkutsk, 664033
Е. Oborina
A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: mir@irioch.irk.ru
Rússia, ul. Favorskogo 1, Irkutsk, 664033
I. Ushakov
Irkutsk National Research Technical University
Email: mir@irioch.irk.ru
Rússia, Irkutsk
А. Mirskova
A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: mir@irioch.irk.ru
Rússia, ul. Favorskogo 1, Irkutsk, 664033
