Heterocycle‐Tethered Aurones: Synthesis and Evaluation of α‐Glucosidase Inhibition.
A wide range of heterocycle‐tethered aurones were synthesized using an efficient approach for the capture of in situ generated aurone‐based ortho‐quinone methide intermediates by 3‐(2‐hydroxyphenyl)enaminones and further ring‐opening and ring‐closure reaction with bidentate nucleophiles. The synthes...
| Publicado en: | BioMed Research International Vol. 2026; pp. 1 - 15 |
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| Autores principales: | , , , , , , |
| Formato: | pictorial research tables/charts Journal Article |
| Publicado: |
Wiley-Blackwell
4/17/2026
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| Acceso en línea: | Ver este registro en EBSCOhost |