Journals / Turkish Journal of Chemistry / 2003 / Cilt: 27 - Sayı: 1

An Efficient Synthesis of Alnustone, a Naturally Occurring Compound

Pages
31–34
Publication Date
2003-01-01
DOI
—
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AI Summary & Key Takeaways

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

Alnustone, 4(E),6(E)-1,7-diphenyl-hepta-4,6-dien-3-one, was synthesized starting from benzaldehyde in three steps with an overall yield of 57%.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Alnustone, 4(E),6(E)-1,7-diphenyl-hepta-4,6-dien-3-one, was synthesized starting from benzaldehyde in three steps with an overall yield of 57%.
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Key Findings & Data:The condensation of benzaldehyde with acetone gave benzalacetone.
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Conclusion & Impact:The in situ enamination of benzylacetone with pyrrolidine and acetic acid followed by cinnamaldehyde treatment gave alnustone.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:alnustone · 4(E) · 6(E)-1

Abstract

Alnustone, 4(E),6(E)-1,7-diphenyl-hepta-4,6-dien-3-one, was synthesized starting from benzaldehyde in three steps with an overall yield of 57%. The condensation of benzaldehyde with acetone gave benzalacetone. The Pd-C catalyzed hydrogenation of benzalacetone afforded benzylacetone. The in situ enamination of benzylacetone with pyrrolidine and acetic acid followed by cinnamaldehyde treatment gave alnustone.

Özet

Alnustone, 4(E),6(E)-1,7-diphenyl-hepta-4,6-dien-3-one, was synthesized starting from benzaldehyde in three steps with an overall yield of 57%. The condensation of benzaldehyde with acetone gave benzalacetone. The Pd-C catalyzed hydrogenation of benzalacetone afforded benzylacetone. The in situ enamination of benzylacetone with pyrrolidine and acetic acid followed by cinnamaldehyde treatment gave alnustone.

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Cite This Article

GÖKSU, S., ÇELİK, H., SEÇEN, H. (2003). An Efficient Synthesis of Alnustone, a Naturally Occurring Compound. Turkish Journal of Chemistry, Cilt: 27 - Sayı: 1, 31–34. https://ajindex.com/articles/393408

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