Direction of alkylation of 5-aryl-1,3,4-oxadiazoline-2-thiones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1997-09

AUTHORS

A. A. Ziyaev, G. G. Galust'yan

ABSTRACT

The reaction of potassium salt of 5-(2,4-dichlorophenyl)-1,3,4-oxadiazoline-2-thione with dimethyl sulfate was carried out in water and HMPT. It was shown that the nature of the solvent affects the ratio of the formed products of S- and N-methylation. The alkylation of 5-aryl-1,3,4-oxadiazoline-2-thiones with isomeric butyl chlorides showed that the reaction takes place only with n-butyl chloride with the formation of the corresponding S-butyl-substituted derivative. More... »

PAGES

1109-1111

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf02253229

DOI

http://dx.doi.org/10.1007/bf02253229

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1000649390


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