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Related Datasets
1 of 3
A quantitative approach to predicting rate constants for aqueous racemization allows pointless stereoselective syntheses to be avoided - Ballard A, Buurma NJ (2017). Cardiff University. 10.17035/d.2017.0043106638. Chemical reaction dynamics and mechanisms Chemical synthesis Catalysis and surfaces Chemical measurement
Borane Catalyzed Stereoselective C–H insertion, Cyclopropanation, and Ring-Opening Reactions - data - Dasgupta A, Babaahmadi R, Slater B, et al. (2020). Cardiff University. 10.17035/d.2020.0111365980. Catalysis and surfaces Chemical synthesis
Chiral carbene–borane adducts: precursors for borenium catalysts for asymmetric FLP hydrogenations - Lam J, Günther BAR, Farrell JM, et al. (2016). Cardiff University. 10.17035/d.2016.0011648516. Chemical synthesis Chemical X-ray Crystallography Chemical Synthetic Methodology Imines
Contrasting frustrated Lewis pair reactivity with selenium- and boron-based Lewis acids - Wilkins LC, Gunther BAR, Walther M, et al. (2017). Cardiff University. 10.17035/d.2017.0011648620. Chemical synthesis
Copper(II) complexes of pyridine-oxazoline (Pyox) ligands: coordination chemistry, ligand stability and catalysis - Ward BD, Hallett AJ, Kariuki B (2016). Cardiff University. 10.17035/d.2015.100130. Chemical synthesis
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Last updated on 2015-10-11 at 12:52
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