New Method of Synthesis of Biologically Active Get(aryl)chalcogenylacetates of Tris(2-hydroxyethyl)ammonium View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-10

AUTHORS

S. N. Adamovich, Е. N. Oborina, I. А. Ushakov, А. N. Mirskova

ABSTRACT

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%).

PAGES

2227-2229

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363218100353

DOI

http://dx.doi.org/10.1134/s1070363218100353

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1110193362


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