Journal article
Authors list: Ghorai, D; Müller, V; Keil, H; Stalke, D; Zanoni, G; Tkachenko, BA; Schreiner, PR; Ackermann, L
Publication year: 2017
Pages: 3137-3141
Journal: Advanced Synthesis & Catalysis
Volume number: 359
Issue number: 18
DOI Link: https://doi.org/10.1002/adsc.201700663
Publisher: Wiley
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.
Abstract:
Citation Styles
Harvard Citation style: Ghorai, 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 style: Ghorai, 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