| Merging organocatalysis and gold catalysis—a critical evaluation of the underlying concepts CCJ Loh, D Enders Chemistry–A European Journal 18 (33), 10212-10225, 2012 | 242 | 2012 |
| Exploiting the electrophilic properties of indole intermediates: new options in designing asymmetric reactions CCJ Loh, D Enders Angewandte Chemie International Edition 1 (51), 46-48, 2011 | 145 | 2011 |
| Merging organocatalysis and gold catalysis: enantioselective synthesis of tetracyclic indole derivatives through a sequential double friedel–crafts type reaction CCJ Loh, J Badorrek, G Raabe, D Enders Chemistry–A European Journal 48 (17), 13409-13414, 2011 | 144 | 2011 |
| Streocontrolled construction of six vicinal stereogenic centers on spiropyrazolones via organocascade Michael/Michael/1, 2-addition reactions P Chauhan, S Mahajan, CCJ Loh, G Raabe, D Enders Organic letters 16 (11), 2954-2957, 2014 | 136 | 2014 |
| Asymmetric synthesis of pyrroloindolones by N-heterocyclic carbene catalyzed [2+ 3] annulation of α-chloroaldehydes with nitrovinylindoles. Q Ni, H Zhang, A Grossmann, CCJ Loh, C Merkens, D Enders Angewandte Chemie International Edition 52 (51), 2013 | 129 | 2013 |
| Organocatalytic, Asymmetric Synthesis of 3‐Sulfenylated N‐Boc‐Protected Oxindoles C Wang, X Yang, CCJ Loh, G Raabe, D Enders Chemistry-a European Journal 18 (37), 11531, 2012 | 83 | 2012 |
| Exploiting non-covalent interactions in selective carbohydrate synthesis CCJ Loh Nature Reviews Chemistry 5 (11), 792-815, 2021 | 82 | 2021 |
| Enantioselective Synthesis of Tetrahydrocarbazoles through a Michael Addition/Ciamician–Plancher Rearrangement Sequence: Asymmetric Synthesis of a Potent Constrained Analogue … CCJ Loh, G Raabe, D Enders Chemistry-a European Journal 18 (42), 13250, 2012 | 76 | 2012 |
| A multistage halogen bond catalyzed strain-release glycosylation unravels new hedgehog signaling inhibitors C Xu, CCJ Loh Journal of the American Chemical Society 141 (13), 5381-5391, 2019 | 71 | 2019 |
| Asymmetric organocatalytic Michael/Henry domino reactions through hydrogen-bond activation: kinetic access to indane scaffolds bearing cis-vicinal substituents. CCJ Loh, I Atodiresei, D Enders Chemistry-A European Journal 19 (33), 2013 | 61 | 2013 |
| Rhodium-catalyzed allylation reactions MB Thoke, Q Kang Synthesis 51 (13), 2585-2631, 2019 | 59 | 2019 |
| Asymmetric domino synthesis of indanes bearing four contiguous stereocentres catalyzed by sub-mol% loadings of a squaramide in minutes CCJ Loh, D Hack, D Enders Chemical Communications 49 (87), 10230-10232, 2013 | 53 | 2013 |
| A robust and tunable halogen bond organocatalyzed 2-deoxyglycosylation involving quantum tunneling C Xu, VUB Rao, J Weigen, CCJ Loh Nature communications 11 (1), 4911, 2020 | 46 | 2020 |
| Ausnutzung der elektrophilen Eigenschaften von Indol‐Intermediaten: neue Optionen in der Planung asymmetrischer Reaktionen CCJ Loh, D Enders Angewandte Chemie 1 (124), 46-49, 2011 | 46 | 2011 |
| Exploiting Distal Reactivity of Coumarins: A Rhodium‐Catalyzed Vinylogous Asymmetric Ring‐Opening Reaction CCJ Loh, M Schmid, B Peters, X Fang, M Lautens Angewandte Chemie International Edition 55 (14), 4600-4604, 2016 | 45 | 2016 |
| An ultra-low thiourea catalyzed strain-release glycosylation and a multicatalytic diversification strategy C Xu, CCJ Loh Nature Communications 9 (1), 4057, 2018 | 37 | 2018 |
| Enantioselective organocatalytic domino synthesis of tetrahydropyridin-2-ols JP Wan, CCJ Loh, F Pan, D Enders Chemical Communications 48 (80), 10049-10051, 2012 | 36 | 2012 |
| Thiourea-catalyzed domino Michael–Mannich [3+ 2] cycloadditions: A strategy for the asymmetric synthesis of 3, 3′-pyrrolidinyl-dispirooxindoles Y Zhi, K Zhao, C von Essen, K Rissanen, D Enders Synlett 28 (20), 2876-2880, 2017 | 33 | 2017 |
| Rhodium‐Catalyzed Asymmetric Cycloisomerization and Parallel Kinetic Resolution of Racemic Oxabicycles CCJ Loh, M Schmid, R Webster, A Yen, SK Yazdi, PT Franke, M Lautens Angewandte Chemie International Edition 55 (34), 10074-10078, 2016 | 32 | 2016 |
| Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth‐Generation Rhodium Catalytic System CCJ Loh, X Fang, B Peters, M Lautens Chemistry–A European Journal 21 (40), 13883-13887, 2015 | 32 | 2015 |
Mark LautensProfessor of ChemistryVerified email at utoronto.ca
