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...
| Published in: | BioMed Research International Vol. 2026; pp. 1 - 15 |
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| Main Authors: | , , , , , , |
| Format: | pictorial research tables/charts Journal Article |
| Published: |
Wiley-Blackwell
4/17/2026
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| Online Access: | View this record in EBSCOhost |