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Synthesis and characterization of novel unnatural bichalcones

Five bichalcones ( 5-1 ∼ 5-4 , 9 ) were prepared by the reaction of biphenyl-4,4′-dicarbaldehyde ( 4 ) and 4,4′-dioxybenzaldehyde ( 8 ) with the respective acetophenone analogs via Claisen-Schmidt condensation and were then fully identified by 1H-NMR, 13 C-NMR and mass analyses.

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Bibliographic Details
Published in:Archives of pharmacal research 2010, 33(12), , pp.1919-1926
Main Authors: Gurung, Santosh K., Kim, Soo Bae, Park, Haeil
Format: Article
Language:English
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Summary:Five bichalcones ( 5-1 ∼ 5-4 , 9 ) were prepared by the reaction of biphenyl-4,4′-dicarbaldehyde ( 4 ) and 4,4′-dioxybenzaldehyde ( 8 ) with the respective acetophenone analogs via Claisen-Schmidt condensation and were then fully identified by 1H-NMR, 13 C-NMR and mass analyses.
ISSN:0253-6269
1976-3786
DOI:10.1007/s12272-010-1205-2