Journal article

Secondary Phosphine Oxide Preligands for Palladium‐Catalyzed C–H (Hetero)Arylations: Efficient Access to Pybox Ligands


Authors listGhorai, D; Müller, V; Keil, H; Stalke, D; Zanoni, G; Tkachenko, BA; Schreiner, PR; Ackermann, L

Publication year2017

Pages3137-3141

JournalAdvanced Synthesis & Catalysis

Volume number359

Issue number18

DOI Linkhttps://doi.org/10.1002/adsc.201700663

PublisherWiley


Abstract

C–H arylations of oxazolines were accomplished with a well‐defined palladium catalyst derived from a secondary bisdiamantyl phosphine oxide. The single‐component secondary phosphine oxide (SPO)‐palladium complex enabled C–H activations with aryl bromides and challenging aryl chlorides in the absence of directing groups, setting the stage for the step‐economical synthesis of pybox ligands under racemization‐free reaction conditions.




Citation Styles

Harvard Citation styleGhorai, D., Müller, V., Keil, H., Stalke, D., Zanoni, G., Tkachenko, B., et al. (2017) Secondary Phosphine Oxide Preligands for Palladium‐Catalyzed C–H (Hetero)Arylations: Efficient Access to Pybox Ligands, Advanced Synthesis & Catalysis, 359(18), pp. 3137-3141. https://doi.org/10.1002/adsc.201700663

APA Citation styleGhorai, D., Müller, V., Keil, H., Stalke, D., Zanoni, G., Tkachenko, B., Schreiner, P., & Ackermann, L. (2017). Secondary Phosphine Oxide Preligands for Palladium‐Catalyzed C–H (Hetero)Arylations: Efficient Access to Pybox Ligands. Advanced Synthesis & Catalysis. 359(18), 3137-3141. https://doi.org/10.1002/adsc.201700663


Last updated on 2025-21-05 at 14:52