Synthesis and Antimicrobial Activity of Newly Synthesized Substituted 3-flavanol
Corresponding Author(s) : P.S. Utale
Asian Journal of Chemistry,
Vol. 11 No. 2 (1999): Vol 11 Issue 2
Abstract
2´-Hydroxy-5´-chlorochalcone and its derivatives react with
H2O2 in presence of NaOH to give 6-chloro-3-flavanol and its
derivatives. These synthesised compounds were tested against
test organisms Staphylococcus aurecus, Staphylococous pyrogens,
S. agalactiae, S. faecalis, Corynebacterium ulcerans, C.
minutissimum, Clostridum septicum, Clostridium tetani and
Escherichia coli. The % MIC values were determined by using
serial dilution method.
Keywords
Synthesis
Antimicrobial Activity
Newly Synthesized
Substituted 3-flavanol
Utale, P., Raghuwanshi, P., & Doshi, A. (2010). Synthesis and Antimicrobial Activity of Newly Synthesized Substituted 3-flavanol. Asian Journal of Chemistry, 11(2), 644–646. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/23336
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