| Understanding chemical reactivity using the activation strain model FMBTAH Pascal Vermeeren, Stephanie C. C. van der Lubbe, Célia Fonseca Guerra Nature Protocols 15, 649-667, 2020 | 300 | 2020 |
| Nucleophilic Substitution (SN2): Dependence on Nucleophile, Leaving Group, Central Atom, Substituents, and Solvent TA Hamlin, M Swart, FM Bickelhaupt ChemPhysChem 19 (11), 1315-1330, 2018 | 276 | 2018 |
| How Lewis Acids Catalyze Diels–Alder Reactions P Vermeeren, TA Hamlin, I Fernández, FM Bickelhaupt Angewandte Chemie 132 (15), 6260-6265, 2020 | 200 | 2020 |
| Chemical reactivity from an activation strain perspective P Vermeeren, TA Hamlin, FM Bickelhaupt Chemical Communications 57 (48), 5880-5896, 2021 | 133 | 2021 |
| The Pauli repulsion-lowering concept in catalysis TA Hamlin, FM Bickelhaupt, I Fernández Accounts of Chemical Research 54 (8), 1972-1981, 2021 | 122 | 2021 |
| Oxoammonium salt oxidations of alcohols in the presence of pyridine bases JM Bobbitt, AL Bartelson, WF Bailey, TA Hamlin, CB Kelly The Journal of Organic Chemistry 79 (3), 1055-1067, 2014 | 109 | 2014 |
| How dihalogens catalyze Michael addition reactions TA Hamlin, I Fernández, FM Bickelhaupt Angewandte Chemie International Edition 58 (26), 8922-8926, 2019 | 106 | 2019 |
| PyFrag 2019—Automating the exploration and analysis of reaction mechanisms X Sun, TM Soini, J Poater, TA Hamlin, FM Bickelhaupt Journal of Computational Chemistry 40 (25), 2227-2233, 2019 | 93 | 2019 |
| Origin of the α‐Effect in SN2 Reactions T Hansen, P Vermeeren, FM Bickelhaupt, TA Hamlin Angewandte Chemie International Edition 60 (38), 20840-20848, 2021 | 91 | 2021 |
| Oxidation of α-Trifluoromethyl alcohols using a recyclable oxoammonium salt CB Kelly, MA Mercadante, TA Hamlin, MH Fletcher, NE Leadbeater The Journal of Organic Chemistry 77 (18), 8131-8141, 2012 | 88 | 2012 |
| Toward a unified mechanism for oxoammonium salt-mediated oxidation reactions: a theoretical and experimental study using a hydride transfer model TA Hamlin, CB Kelly, JM Ovian, RJ Wiles, LJ Tilley, NE Leadbeater The Journal of Organic Chemistry 80 (16), 8150-8167, 2015 | 87 | 2015 |
| Regioselectivity of Epoxide Ring‐Openings via SN2 Reactions Under Basic and Acidic Conditions T Hansen, P Vermeeren, A Haim, MJH van Dorp, JDC Codée, ... European Journal of Organic Chemistry 2020 (25), 3822-3828, 2020 | 83 | 2020 |
| How oriented external electric fields modulate reactivity S Yu, P Vermeeren, TA Hamlin, FM Bickelhaupt Chemistry–A European Journal 27 (18), 5683-5693, 2021 | 78 | 2021 |
| Chemoselectivity of Tertiary Azides in Strain‐Promoted Alkyne‐Azide Cycloadditions D Svatunek, N Houszka, TA Hamlin, FM Bickelhaupt, H Mikula Chemistry–A European Journal 25 (3), 754-758, 2019 | 76 | 2019 |
| Origin of rate enhancement and asynchronicity in iminium catalyzed Diels–Alder reactions P Vermeeren, TA Hamlin, I Fernández, FM Bickelhaupt Chemical Science 11 (31), 8105-8112, 2020 | 75 | 2020 |
| Structural distortion of cycloalkynes influences cycloaddition rates both by strain and interaction energies TA Hamlin, BJ Levandowski, AK Narsaria, KN Houk, FM Bickelhaupt Chemistry–A European Journal 25 (25), 6342-6348, 2019 | 73 | 2019 |
| Role of orbital interactions and activation strain (distortion energies) on reactivities in the normal and inverse electron-demand cycloadditions of strained and unstrained … BJ Levandowski, TA Hamlin, FM Bickelhaupt, KN Houk The Journal of organic chemistry 82 (16), 8668-8675, 2017 | 71 | 2017 |
| The pnictogen bond: A quantitative molecular orbital picture L de Azevedo Santos, TA Hamlin, TC Ramalho, FM Bickelhaupt Physical Chemistry Chemical Physics 23 (25), 13842-13852, 2021 | 65 | 2021 |
| Nucleophilic substitution in solution: activation strain analysis of weak and strong solvent effects TA Hamlin, B van Beek, LP Wolters, FM Bickelhaupt Chemistry–A European Journal 24 (22), 5927-5938, 2018 | 65 | 2018 |
| A quantitative molecular orbital perspective of the chalcogen bond L de Azevedo Santos, SCC van Der Lubbe, TA Hamlin, TC Ramalho, ... ChemistryOpen 10 (4), 391-401, 2021 | 62 | 2021 |
