| Defining the SN1 Side of Glycosylation Reactions: Stereoselectivity of Glycopyranosyl Cations T Hansen, L Lebedel, WA Remmerswaal, S van Der Vorm, DPA Wander, ... ACS central science 5 (5), 781-788, 2019 | 123* | 2019 |
| Characterization of glycosyl dioxolenium ions and their role in glycosylation reactions T Hansen, H Elferink, JMA van Hengst, KJ Houthuijs, WA Remmerswaal, ... Nature Communications 11 (1), 2664, 2020 | 122 | 2020 |
| Stabilization of Glucosyl Dioxolenium Ions by “Dual Participation” of the 2,2-Dimethyl-2-(ortho-nitrophenyl)acetyl (DMNPA) Protection Group for 1,2-cis-Glucosylation WA Remmerswaal, KJ Houthuijs, R Van De Ven, H Elferink, T Hansen, ... The Journal of Organic Chemistry 87 (14), 9139-9147, 2022 | 19 | 2022 |
| Halogen atom participation in guiding the stereochemical outcomes of acetal substitution reactions KM Demkiw, WA Remmerswaal, T Hansen, GA van der Marel, ... Angewandte Chemie International Edition 61 (42), e202209401, 2022 | 16 | 2022 |
| Mapping the effect of configuration and protecting group pattern on glycosyl acceptor reactivity JMA van Hengst, RJC Hellemons, WA Remmerswaal, ... Chemical Science 14 (6), 1532-1542, 2023 | 15 | 2023 |
| Competing C‐4 and C‐5‐acyl stabilization of uronic acid glycosyl cations H Elferink, WA Remmerswaal, KJ Houthuijs, O Jansen, T Hansen, AM Rijs, ... Chemistry–A European Journal 28 (63), e202201724, 2022 | 13 | 2022 |
| Anomeric Triflates versus Dioxanium Ions: Different Product-Forming Intermediates from 3-Acyl Benzylidene Mannosyl and Glucosyl Donors WA Remmerswaal, H Elferink, KJ Houthuijs, T Hansen, F Ter Braak, ... The Journal of Organic Chemistry 89 (3), 1618-1625, 2024 | 11* | 2024 |
| Neighboring‐Group Participation by C‐2 Acyloxy Groups: Influence of the Nucleophile and Acyl Group on the Stereochemical Outcome of Acetal Substitution Reactions Y Chun, WA Remmerswaal, JDC Codée, KA Woerpel Chemistry–A European Journal 29 (57), e202301894, 2023 | 9 | 2023 |
| Origin of Stereoselectivity in SE2′ Reactions of Six‐membered Ring Oxocarbenium Ions WA Remmerswaal, T Hansen, TA Hamlin, JDC Codée Chemistry–A European Journal 29 (14), e202203490, 2023 | 6 | 2023 |
| JDC Codée in Comprehensive Glycoscience T Hansen, S van der Vorm, C Tugny, WA Remmerswaal, JMA van Hengst, ... Elsevier, Oxford, 2021 | 5 | 2021 |
| Stereoelectronic Effects in Glycosylation Reactions T Hansen, S van der Vorm, C Tugny, WA Remmerswaal, JMA van Hengst, ... Comprehensive Glycoscience: Volume 2, 83-102, 2021 | 3 | 2021 |
| Backside versus Frontside SN2 Reactions of Alkyl Triflates and Alcohols WA Remmerswaal, T de Jong, KNA van de Vrande, R Louwersheimer, ... Chemistry–A European Journal 30 (25), e202400590, 2024 | 1 | 2024 |
| The influence of acceptor acidity on hydrogen bond mediated aglycone delivery (HAD) through the picoloyl protecting group WA Remmerswaal, D Hoogers, M Hoopman, GA Van der Marel, ... European Journal of Organic Chemistry 27 (7), e202301063, 2024 | 1 | 2024 |
| Neighboring-Group Participation by a Less Electron-Donating, Participating C-2-Ester Ensures Higher 1,2-trans Stereoselectivity in Nucleophilic Substitution … Y Chun, WA Remmerswaal, JDC Codée, KA Woerpel The Journal of Organic Chemistry, 2025 | | 2025 |
| Computational and experimental studies of reactive intermediates in glycosylation reactions WA Remmerswaal Leiden University, 2024 | | 2024 |
| How configuration and protecting group pattern influence glycosyl acceptor reactivity JMA van Hengst, RJC Hellemons, WA Remmerswaal, T Hansen, ... Structure-reactivity relationships in glycosylation chemistry 14, 113, 2023 | | 2023 |
| Acceptor nucleophilicity–Glycosylation stereoselectivity mapping for all eight diastereomeric pyranosyl donors JMA van Hengst, WA Remmerswaal, T Hansen, HS Overkleeft, ... Structure-reactivity relationships in glycosylation chemistry, 83, 0 | | |
| Stereoselectivity of SN1-like reactions of all eight diastereoisomeric pyranosyl and 6-deoxy pyranosyl donors with D-or C-nucleophiles JMA van Hengst, WA Remmerswaal, T Hansen Structure-reactivity relationships in glycosylation chemistry, 33, 0 | | |