Ian J. S. Fairlamb
Affiliations: | University of York, York, England, United Kingdom |
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"Ian Fairlamb"Mean distance: 8.82
Parents
Sign in to add mentor| Julia M. Dickinson | grad student | Manchester Metropolitan University | |
| Guy Lloyd-Jones | post-doc | University of Bristol |
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Publications
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| Aoki Y, Bauer M, Braun T, et al. (2019) Physical methods for mechanistic understanding: general discussion. Faraday Discussions |
| Aoki Y, Braun T, Davies D, et al. (2019) Understanding unusual element-element bond formation and activation: general discussion. Faraday Discussions |
| Wenzel MN, Owens PK, Bray JT, et al. (2017) Redox Couple Involving NOx in Aerobic Pd-Catalyzed Oxidation of sp(3)-C-H Bonds: Direct Evidence for Pd-NO3(-)/NO2(-) Interactions Involved in Oxidation and Reductive Elimination. Journal of the American Chemical Society |
| Younesi Y, Nasiri B, BabaAhmadi R, et al. (2016) Theoretical rationalisation for the mechanism of N-heterocyclic carbene-halide reductive elimination at Cu(III), Ag(III) and Au(III). Chemical Communications (Cambridge, England) |
| Fairlamb I, Reay A, Neumann L. (2016) Catalyst Efficacy of Homogeneous and Heterogeneous Palladium Catalysts in the Direct Arylation of Common Heterocycles Synlett. 27: 1211-1216 |
| Ronson TO, Burns MJ, Voelkel MH, et al. (2015) Total Synthesis and Stereochemical Revision of Phacelocarpus 2-Pyrone A. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Reay AJ, Fairlamb IJ. (2015) Catalytic C-H bond functionalisation chemistry: the case for quasi-heterogeneous catalysis. Chemical Communications (Cambridge, England). 51: 16289-307 |
| Fairlamb IJ. (2015) Redox-Active NOx Ligands in Palladium-Mediated Processes. Angewandte Chemie (International Ed. in English) |
| Reay AJ, Williams TJ, Fairlamb IJ. (2015) Unified mild reaction conditions for C2-selective Pd-catalysed tryptophan arylation, including tryptophan-containing peptides. Organic & Biomolecular Chemistry. 13: 8298-309 |
| Ronson TO, Voelkel MH, Taylor RJ, et al. (2015) Macrocyclic polyenynes: a stereoselective route to vinyl-ether-containing skipped diene systems. Chemical Communications (Cambridge, England). 51: 8034-6 |