Dr Paul Dingwall
Dr Paul Dingwall
Lecturer in Physical Organic Chemistry, Queen's University Belfast
Verified email at qub.ac.uk
Cited by
Cited by
The Houk–List transition states for organocatalytic mechanisms revisited
A Armstrong, RA Boto, P Dingwall, J Contreras-García, MJ Harvey, ...
Chemical Science 5 (5), 2057-2071, 2014
Chemoselective polymerizations from mixtures of epoxide, lactone, anhydride, and carbon dioxide
C Romain, Y Zhu, P Dingwall, S Paul, HS Rzepa, A Buchard, CK Williams
Journal of the American Chemical Society 138 (12), 4120-4131, 2016
High power Nb-doped LiFePO4 Li-ion battery cathodes; pilot-scale synthesis and electrochemical properties
ID Johnson, E Blagovidova, PA Dingwall, DJL Brett, PR Shearing, JA Darr
Journal of Power Sources 326, 476-481, 2016
Understanding a hydroformylation catalyst that produces branched aldehydes from alkyl alkenes
P Dingwall, JA Fuentes, L Crawford, AMZ Slawin, M Buhl, ML Clarke
Journal of the American Chemical Society 139 (44), 15921-15932, 2017
Ruthenium (II) and osmium (II) vinyl complexes as highly sensitive and selective chromogenic and fluorogenic probes for the sensing of carbon monoxide in air
A Toscani, C Marin-Hernandez, ME Moragues Pons, F Sancenón Galarza, ...
Chemistry-A European Journal 21 (41), 14529-14538, 2015
Rationalization of an Unusual Solvent‐Induced Inversion of Enantiomeric Excess in Organocatalytic Selenylation of Aldehydes
J Burés, P Dingwall, A Armstrong, DG Blackmond
Angewandte Chemie International Edition 53 (33), 8700-8704, 2014
Highly sensitive and selective molecular probes for chromo-fluorogenic sensing of carbon monoxide in air, aqueous solution and cells
A Toscani, C Marin-Hernandez, J Robson, E Chua, P Dingwall, A White, ...
Wiley, 2019
Fast continuous alcohol amination employing a hydrogen borrowing protocol
R Labes, C Mateos, C Battilocchio, Y Chen, P Dingwall, GR Cumming, ...
Green Chemistry 21 (1), 59-63, 2019
Photochemical Homologation for the Preparation of Aliphatic Aldehydes in Flow
Y Chen, M Leonardi, P Dingwall, R Labes, P Pasau, DC Blakemore, ...
The Journal of organic chemistry 83 (24), 15558-15568, 2018
C–H functionalisation of aldehydes using light generated, non-stabilised diazo compounds in flow
P Dingwall, A Greb, LNS Crespin, R Labes, B Musio, JS Poh, P Pasau, ...
Chemical Communications 54 (83), 11685-11688, 2018
CO‐Free Enantioselective Hydroformylation of Functionalised Alkenes: Using a Dual Catalyst System to Give Improved Selectivity and Yield
R Pittaway, P Dingwall, JA Fuentes, ML Clarke
Advanced Synthesis & Catalysis 361 (18), 4334-4341, 2019
Understanding Catalyst Structure–Selectivity Relationships in Pd-Catalyzed Enantioselective Methoxycarbonylation of Styrene
S Gallarati, P Dingwall, JA Fuentes, M Bühl, ML Clarke
Organometallics, 2020
Composition of catalyst resting states of hydroformylation catalysts derived from bulky mono-phosphorus ligands, rhodium dicarbonyl acetylacetonate and syngas
RC How, P Dingwall, RT Hembre, JA Ponasik, GS Tolleson, ML Clarke
Molecular Catalysis 434, 116-122, 2017
Atroposelective Synthesis, Structure and Properties of a Novel Class of Axially Chiral N‐Aryl Quinolinium Salt
JS Sweet, S Rajkumar, P Dingwall, PC Knipe
European Journal of Organic Chemistry, 2021
Data supporting" Photochemical homologation for the preparation of aliphatic aldehydes in flow"
Y Chen, M Leonardi, P Dingwall, P Pasau, D Blakemore, S Ley
Research data supporting" CH Functionalisation of Aldehydes using Light Generated, Non-Stabilised Diazo Compounds in Flow"
PA Dingwall, A Greb, LNS Crespin, R Labes, B Musio, JS Poh, P Pasau, ...
Mechanistic Understanding of Proline Analogs and Related Protic Lewis Bases (n → π*)
A Armstrong, P Dingwall
Lewis Base Catalysis in Organic Synthesis, 145-190, 2016
Mechanistic insights into organocatalysis
PA Dingwall
Imperial College London, 2013
Figure 11. Chemo-Selective Polymerizations Using Mixtures of Epoxide, Lactone, Anhydride and CO2
HS Rzepa, C Romain, P Dingwall, Y Zhu, S Paul, A Buchard, C K Williams
Figure 10. Chemo-Selective Polymerizations Using Mixtures of Epoxide, Lactone, Anhydride and CO2. Figure 13.
HS Rzepa, C Romain, P Dingwall, Y Zhu, S Paul, A Buchard, C K Williams
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