An industrial perspective on counter anions in gold catalysis: underestimated with respect to “Ligand effects”

The conversion of a variety of well-known test reactions, representing the key reactivity patterns of gold catalysis, were analyzed by GC and 1H NMR. The study is focused on establishing of a strategical approach for the consideration of ligand influence and counter anion influence during the cataly...

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Main Authors: Schießl, Jasmin (Author) , Schulmeister, Jürgen (Author) , Doppiu, Angelino (Author) , Wörner, Eileen (Author) , Rudolph, Matthias (Author) , Karch, Ralf (Author) , Hashmi, A. Stephen K. (Author)
Format: Article (Journal)
Language:English
Published: 25 March 2018
In: Advanced synthesis & catalysis
Year: 2018, Volume: 360, Issue: 13, Pages: 2493-2502
ISSN:1615-4169
DOI:10.1002/adsc.201800233
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/adsc.201800233
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.201800233
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Author Notes:Jasmin Schießl, Jürgen Schulmeister, Angelino Doppiu, Eileen Wörner, Matthias Rudolph, Ralf Karch, A. Stephen K. Hashmi
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Summary:The conversion of a variety of well-known test reactions, representing the key reactivity patterns of gold catalysis, were analyzed by GC and 1H NMR. The study is focused on establishing of a strategical approach for the consideration of ligand influence and counter anion influence during the catalyst optimization including an industrial perspective. The study shows a dominance of the counter anion, a dominance which up to now has been neglected in most of the routine screenings. In addition, a drastic substrate-dependency became obvious, even a marginal variation of the substrate already could strongly effect the catalytic activity and change the optimal counter anion or ligand. Based on the collected data a strategic concept for an efficient screening for a specific substrate is introduced, this concept can serve as an important guideline for catalyst optimization in homogeneous gold catalysis.
Item Description:Gesehen am 21.04.2020
Physical Description:Online Resource
ISSN:1615-4169
DOI:10.1002/adsc.201800233