Addition of Carboxylic Acids to gem-Difluoroalkenes for the Synthesis of gem-Difluoromethylenated Compounds

We herein describe a straightforward protocol for the synthesis of carboxylic esters containing a gem-difluoromethylene unit. Readily available carboxylic acids can act as nucleophiles to add regioselectively to tetrasubstituted or trisubstituted β,β-difluoroacrylates (formal hydroacetoxylation) for...

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Veröffentlicht in:Organic letters 2024-02, Vol.26 (6), p.1261-1264
Hauptverfasser: Zong, Yuwei, Tsui, Gavin Chit
Format: Artikel
Sprache:eng
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Zusammenfassung:We herein describe a straightforward protocol for the synthesis of carboxylic esters containing a gem-difluoromethylene unit. Readily available carboxylic acids can act as nucleophiles to add regioselectively to tetrasubstituted or trisubstituted β,β-difluoroacrylates (formal hydroacetoxylation) for the construction of RCO2–CF2 bonds. Thermal conditions are sufficient without the use of catalysts or additives.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.4c00095