Journals / Turkish Journal of Chemistry / 2020 / Cilt: 44 - Sayı: 3

Syntheses and antibacterial activities of 4 linear nonphenolic diarylheptanoids

Pages
589–601
Publication Date
2020-06-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

All of the synthesized compound exhibited different degrees of antimicrobial activity at concentrations between 20-100 μg/disc against the test organisms.

📌 3 Key Takeaways

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Objective & Hypothesis:Four linear nonphenolic diarylheptanoids were synthesized and their antibacterial activities were studied. $S $-2-Me-CBS-catalysed reduction of alnustone with BH$_{3}$.SMe$_{2}$ gave $R $ - 4$E$,6$E $-1,7-diphenylhepta-4,6-dien-3-ol, a natural product.
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Key Findings & Data:Reduction of alnustone with Na in t-BuOH at -15 $^{\circ}$C under NH$_{3}$ atm gave $E $-1,7-diphenylhept-5-en-3-one as a Birch-type reduction product. $t$-BuOK catalysed condensation of benzalacetone with propionyl chloride gave 4$Z$,6$E $-5-hydroxy-1,7-diphenylhepta-4,6-dien-3-one, a natural product. 1$E$,4$Z$,6$E $-5-Hydroxy-4-phenethyl-1,7-diphenylhepta-1,4,6-trien-3-one, a curcuminoid, was synthesized starting from pentan-2,4-dione in 3 steps.
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Conclusion & Impact:All of the synthesized compound exhibited different degrees of antimicrobial activity at concentrations between 20-100 μg/disc against the test organisms.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Linear diarylheptanoid · curcuminoid · alnustone

Abstract

Four linear nonphenolic diarylheptanoids were synthesized and their antibacterial activities were studied. $S $-2-Me-CBS-catalysed reduction of alnustone with BH$_{3}$.SMe$_{2}$ gave $R $ - 4$E$,6$E $-1,7-diphenylhepta-4,6-dien-3-ol, a natural product. Reduction of alnustone with Na in t-BuOH at -15 $^{\circ}$C under NH$_{3}$ atm gave $E $-1,7-diphenylhept-5-en-3-one as a Birch-type reduction product. $t$-BuOK catalysed condensation of benzalacetone with propionyl chloride gave 4$Z$,6$E $-5-hydroxy-1,7-diphenylhepta-4,6-dien-3-one, a natural product. 1$E$,4$Z$,6$E $-5-Hydroxy-4-phenethyl-1,7-diphenylhepta-1,4,6-trien-3-one, a curcuminoid, was synthesized starting from pentan-2,4-dione in 3 steps. The synthesized chemical compounds were applied against 2 gram-positive bacteria Bacillus cereus and Arthrobacter agilis , 4 gram-negative bacteria Pseudomonas aeruginosa, Xanthomonas campestris, Klebsiella oxytoca and Helicobacter pylori , and 1 yeast Candida albicans by the disc diffusion method. All of the synthesized compound exhibited different degrees of antimicrobial activity at concentrations between 20-100 μg/disc against the test organisms.

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Cite This Article

DEMİR, Ş. B., SEÇİNTİ, H., ÇELEBİOĞLU, N., ÖZDAL, M., SEZEN, A., GÜLMEZ, Ö., ALGUR, Ö. F., SEÇEN, H. (2020). Syntheses and antibacterial activities of 4 linear nonphenolic diarylheptanoids. Turkish Journal of Chemistry, Cilt: 44 - Sayı: 3, 589–601. https://ajindex.com/articles/184145

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