English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Unexpected ring closure of 2-(1-(4-fluorophenyl)-5-methyl-1 H -1,2,3-triazole-4-carbonyl)- N -phenylhydrazine-1-carbothioamide ( 3 ) on exposure to sulfuric acid at room temperature for an extended duration (12 h) gave 4-((5-(1-(4-fluorophenyl)-5-methyl-1 H -1,2,3-triazol-4-yl)-1,3,4-thiadiazol-2-yl)amino)benzenesulfonic acid ( 4 ) in 75% yield. The use of sulfuric acid led to sulfonation at the  para -position of the benzene ring in phenyl isothiocyanate. The crystal structure comprises two independent types of molecules of  4  and two disordered ether solvent molecules. The synthesized benzenesulfonic acid inhibits the growth of both  Listeria monocytogenes  and  Escherichia coli  and its activity was comparable to those obtained for ampicillin and vancomycin.

phosphorus, sulfur, and silicon and the related elements

4-((5-(1-(4-Fluorophenyl)-5-methyl-1 H -1,2,3-triazol-4-yl)-1,3,4-thiadiazol-2-yl)amino)benzenesulfonic acid: unexpected synthesis, structure elucidation and antimicrobial activity