2023
DOI: 10.1055/s-0042-1752655
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Nickel-Сatalyzed Carbon–Selenium Bond Formations under Mild Conditions

Abstract: A nickel-catalyzed C–Se cross-coupling between aryl iodides and selenols is described. The newly developed catalytic methodology offers facile access to various unsymmetrical selenium-containing motifs. The reaction features excellent functional group tolerance, wide substrate scope, good efficiency, and operates under mild reaction conditions. Notably, this protocol could be readily scaled up to gram scale without the loss of yield.

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Cited by 3 publications
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References 48 publications
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“…28 Rueping and Yue describe a Ni-catalyzed technique for incorporating selenium atoms at sp 2 sites with aryl iodides as counterparts. 29 Following up on their interest in C-H functionalization, Chen and Zhao report a radical-based approach for accessing isoindolinones with ammonium persulfate as the oxidant. 30 Zhou and Yu describe the utilization of Cp*Rh(III)Cl 2 catalysts for enabling a series of transfer hydrogenation events with isopropanol as the hydride source.…”
Section: Cluster Synlettmentioning
confidence: 99%
“…28 Rueping and Yue describe a Ni-catalyzed technique for incorporating selenium atoms at sp 2 sites with aryl iodides as counterparts. 29 Following up on their interest in C-H functionalization, Chen and Zhao report a radical-based approach for accessing isoindolinones with ammonium persulfate as the oxidant. 30 Zhou and Yu describe the utilization of Cp*Rh(III)Cl 2 catalysts for enabling a series of transfer hydrogenation events with isopropanol as the hydride source.…”
Section: Cluster Synlettmentioning
confidence: 99%