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

A series of novel tetrabromo-α,α’-bis(substituted-benzyl)-cycloalkanones  have been synthesized through a rapid, simple, and efficient methodology in  an excellent isolated yield and characterized via IR, NMR (1H 13C NMR,  DEPT135, DEPT90) and Mass spectrometry. All compounds have been assayed for  in vitro antimicrobial activities against eight bacteria, e. g.  Staphylococcus aureus, Bacillus subtilis, and Listeria monocytogenes,  Salmonella enteritidis, Pseudomonas aeruginosa, Enterobacter aerogenes,  Salmonella typhimurium, and Escherichia coli and five fungi e.g. Botrytis  cinerea, Rhizoctonia solani, Fusarium oxysporum, Sclerotonia sclerotiorum,  and Phytophthora capsici. They showed strong antibacterial activity than  antifungal activities. Compounds 4c, 4d and 4i containing methoxy or chloro  substituent on the para or meta position of the phenyl ring showed comparable  MIC values to streptomycin and tetracycline standard antibiotics. Among all  the tested compounds 4i exhibited good to moderate antifungal activity  against all fungal strains used in the present study

Synthesis and antimicrobial activity of novel tetrabromo-α,α’-bis(substituted-benzyl)cycloalkanones