Journals / Turkish Journal of Chemistry / 2004 / Cilt: 28 - Sayı: 4

Stereoselective Photochemistry of Methoxy Chalcones in Solution and Their Radical Scavenging Activity

Pages
515–521
Publication Date
2004-04-01
DOI
—
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AI Summary & Key Takeaways

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

Precursor chalcones showed high superoxide radical scavenging activity although the dimers were inactive.

📌 3 Key Takeaways

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Objective & Hypothesis:The photochemical dimerization of 3 known methoxy derivatives of chalcones, (2E)-1-(2-methoxy)phenyl-3-phenylpropen-1-one (1), (2E)-1-(3-methoxy)phenyl-3-phenyl-propen-1-one (2), and (2E)-1-(4-methoxy) phenyl-3-phenylpropen-1-one (3), yielded 3 new d -truxinic type dimers in solution: rel-(1b ,2a)- di-(2-methoxy)-benzoyl-rel-(3b ,4a )-diphenylcyclobutane (4), rel-(1b ,2a )-di-(3-methoxy)benzoyl-rel-(3b, 4a )-diphenylcyclobutane (5), and rel-(1b ,2a)- di-(4-methoxy)benzoyl-rel-(3b ,4a )-diphenylcyclobutane (6), stereoselectively.
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Key Findings & Data:The photochemical dimerization of 3 known methoxy derivatives of chalcones, (2E)-1-(2-methoxy)phenyl-3-phenylpropen-1-one (1), (2E)-1-(3-methoxy)phenyl-3-phenyl-propen-1-one (2), and (2E)-1-(4-methoxy) phenyl-3-phenylpropen-1-one (3), yielded 3 new d -truxinic type dimers in solution: rel-(1b ,2a)- di-(2-methoxy)-benzoyl-rel-(3b ,4a )-diphenylcyclobutane (4), rel-(1b ,2a )-di-(3-methoxy)benzoyl-rel-(3b, 4a )-diphenylcyclobutane (5), and rel-(1b ,2a)- di-(4-methoxy)benzoyl-rel-(3b ,4a )-diphenylcyclobutane (6), stereoselectively.
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Conclusion & Impact:Precursor chalcones showed high superoxide radical scavenging activity although the dimers were inactive.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Chalcone · Photodimerizations · Solution

Abstract

The photochemical dimerization of 3 known methoxy derivatives of chalcones, (2E)-1-(2-methoxy)phenyl-3-phenylpropen-1-one (1), (2E)-1-(3-methoxy)phenyl-3-phenyl-propen-1-one (2), and (2E)-1-(4-methoxy) phenyl-3-phenylpropen-1-one (3), yielded 3 new d -truxinic type dimers in solution: rel-(1b ,2a)- di-(2-methoxy)-benzoyl-rel-(3b ,4a )-diphenylcyclobutane (4), rel-(1b ,2a )-di-(3-methoxy)benzoyl-rel-(3b, 4a )-diphenylcyclobutane (5), and rel-(1b ,2a)- di-(4-methoxy)benzoyl-rel-(3b ,4a )-diphenylcyclobutane (6), stereoselectively. Precursor chalcones showed high superoxide radical scavenging activity although the dimers were inactive.

Özet

The photochemical dimerization of 3 known methoxy derivatives of chalcones, (2E)-1-(2-methoxy)phenyl-3-phenylpropen-1-one (1), (2E)-1-(3-methoxy)phenyl-3-phenyl-propen-1-one (2), and (2E)-1-(4-methoxy) phenyl-3-phenylpropen-1-one (3), yielded 3 new d -truxinic type dimers in solution: rel-(1b ,2a)- di-(2-methoxy)-benzoyl-rel-(3b ,4a )-diphenylcyclobutane (4), rel-(1b ,2a )-di-(3-methoxy)benzoyl-rel-(3b, 4a )-diphenylcyclobutane (5), and rel-(1b ,2a)- di-(4-methoxy)benzoyl-rel-(3b ,4a )-diphenylcyclobutane (6), stereoselectively. Precursor chalcones showed high superoxide radical scavenging activity although the dimers were inactive.

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Cite This Article

YAYLI, N., ÜÇÜNCÜ, O., YAŞAR, A., GÖK, Y. (2004). Stereoselective Photochemistry of Methoxy Chalcones in Solution and Their Radical Scavenging Activity. Turkish Journal of Chemistry, Cilt: 28 - Sayı: 4, 515–521. https://ajindex.com/articles/382237

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