Transition metal-free approach for late-stage benzylic C(sp)-H etherifications and esterifications
We report a transition metal-free approach for the regioselective functionalization of benzylic C(sp 3 )-H bonds using alcohols and carboxylic acids as the nucleophiles. This straightforward and general route has provided various benzylic ethers and esters, including twelve pharmaceutically relevant...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2022-10, Vol.58 (81), p.11454-11457 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We report a transition metal-free approach for the regioselective functionalization of benzylic C(sp
3
)-H bonds using alcohols and carboxylic acids as the nucleophiles. This straightforward and general route has provided various benzylic ethers and esters, including twelve pharmaceutically relevant compounds.
Herein, we report a transition metal-free approach for the regioselective functionalisation of benzylic C(sp
3
)-H bonds using alcohols and carboxylic acids as the nucleophiles. Late stage functionalization has been done with complex drug molecules. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d2cc02661a |