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
Hauptverfasser: Zhang, Yu, Sahoo, Prakash Kumar, Ren, Peng, Qin, Yuman, Cauwenbergh, Robin, Nimmegeers, Philippe, SivaRaman, Gandhi, Van Passel, Steven, Guidetti, Andrea, Das, Shoubhik
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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.
ISSN:1359-7345
1364-548X
DOI:10.1039/d2cc02661a