Decarboxylative Negishi Coupling of Redox‐Active Aliphatic Esters by Cobalt Catalysis

A cobalt‐catalyzed decarboxylative Negishi coupling reaction of redox‐active aliphatic esters with organozinc reagents was developed. The method enabled efficient alkyl–aryl, alkyl–alkenyl, and alkyl–alkynyl coupling reactions under mild reaction conditions with no external ligand or additive needed...

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Veröffentlicht in:Angewandte Chemie International Edition 2018-10, Vol.57 (40), p.13096-13100
Hauptverfasser: Liu, Xu‐Ge, Zhou, Chu‐Jun, Lin, E., Han, Xiang‐Lei, Zhang, Shang‐Shi, Li, Qingjiang, Wang, Honggen
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Sprache:eng
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Zusammenfassung:A cobalt‐catalyzed decarboxylative Negishi coupling reaction of redox‐active aliphatic esters with organozinc reagents was developed. The method enabled efficient alkyl–aryl, alkyl–alkenyl, and alkyl–alkynyl coupling reactions under mild reaction conditions with no external ligand or additive needed. The success of an in situ activation protocol and the facile synthesis of the drug molecule (±)‐preclamol highlight the synthetic potential of this method. Mechanistic studies indicated that a radical mechanism is involved. Keen to couple: A cobalt‐catalyzed decarboxylative Negishi coupling reaction of N‐hydroxyphthalimide (NHPI) esters with organozinc reagents enabled efficient alkyl–aryl, alkyl–alkenyl, and alkyl–alkynyl coupling under mild conditions without an external ligand or additive (see scheme). The success of an in situ activation protocol and the facile synthesis of the drug molecule (±)‐preclamol highlight the potential of this method.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201806799