Abstract
A more sustainable and versatile method to access antidiabetic glitazones is demanded. Herein, we report the unprecedented photocatalytic coupling of N-protected methylene thiazolidinediones with radical precursors (organoborates or carboxylic acids) under riboflavin tetraacetate catalysis. The methodology accepts various functional groups and affords (Het)Ar-(CH2)n-thiazolidinediones by transition-metal-free organic photoredox catalysis under mild conditions. The applicability of the developed protocol is showcased by the three-step preparation of the antidiabetic pioglitazone drug.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 10064-10073 |
| Numero di pagine | 10 |
| Rivista | Journal of Organic Chemistry |
| Volume | 90 |
| Numero di pubblicazione | 28 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 2025 |