| N-heterocyclic carbene-functionalized magic-number gold nanoclusters MR Narouz, KM Osten, PJ Unsworth, RWY Man, K Salorinne, S Takano, ... Nature chemistry 11 (5), 419-425, 2019 | 341 | 2019 |
| Modular Synthesis of Triarylmethanes through Palladium‐Catalyzed Sequential Arylation of Methyl Phenyl Sulfone M Nambo, CM Crudden Angewandte Chemie 126 (3), 761-765, 2014 | 173 | 2014 |
| Recent advances in the synthesis of triarylmethanes by transition metal catalysis M Nambo, CM Crudden ACS Catalysis 5 (8), 4734-4742, 2015 | 163 | 2015 |
| Ultrastable Gold Nanoparticles Modified by Bidentate N-Heterocyclic Carbene Ligands RWY Man, CH Li, MWA MacLean, OV Zenkina, MT Zamora, LN Saunders, ... Journal of the American Chemical Society 140 (5), 1576-1579, 2018 | 158 | 2018 |
| Preparation of quaternary centers via nickel-catalyzed suzuki–miyaura cross-coupling of tertiary sulfones ZT Ariki, Y Maekawa, M Nambo, CM Crudden Journal of the American Chemical Society 140 (1), 78-81, 2018 | 129 | 2018 |
| Rh-Catalyzed Arylation and Alkenylation of C60 Using Organoboron Compounds M Nambo, R Noyori, K Itami Journal of the American Chemical Society 129 (26), 8080-8081, 2007 | 125 | 2007 |
| Water‐Soluble N‐Heterocyclic Carbene‐Protected Gold Nanoparticles: Size‐Controlled Synthesis, Stability, and Optical Properties K Salorinne, RWY Man, CH Li, M Taki, M Nambo, CM Crudden Angewandte Chemie International Edition 56 (22), 6198-6202, 2017 | 120 | 2017 |
| Iterative protecting group-free cross-coupling leading to chiral multiply arylated structures CM Crudden, C Ziebenhaus, JPG Rygus, K Ghozati, PJ Unsworth, ... Nature Communications 7 (1), 11065, 2016 | 105 | 2016 |
| Development of versatile sulfone electrophiles for Suzuki–Miyaura cross-coupling reactions M Nambo, EC Keske, JPG Rygus, JCH Yim, CM Crudden ACS Catalysis 7 (2), 1108-1112, 2017 | 96 | 2017 |
| Aziridinofullerene: A versatile platform for functionalized fullerenes M Nambo, Y Segawa, K Itami Journal of the American Chemical Society 133 (8), 2402-2405, 2011 | 95 | 2011 |
| The concise synthesis of unsymmetric triarylacetonitriles via Pd-catalyzed sequential arylation: a new synthetic approach to tri-and tetraarylmethanes M Nambo, M Yar, JD Smith, CM Crudden Organic letters 17 (1), 50-53, 2015 | 94 | 2015 |
| Regioselective Unsymmetrical Tetraallylation of C60 through Palladium Catalysis M Nambo, A Wakamiya, S Yamaguchi, K Itami Journal of the American Chemical Society 131 (42), 15112-15113, 2009 | 78 | 2009 |
| Arylative desulfonation of diarylmethyl phenyl sulfone with arenes catalyzed by scandium triflate M Nambo, ZT Ariki, D Canseco-Gonzalez, DD Beattie, CM Crudden Organic letters 18 (10), 2339-2342, 2016 | 72 | 2016 |
| A bench-stable Pd catalyst for the hydroarylation of fullerene with boronic acids S Mori, M Nambo, LC Chi, J Bouffard, K Itami Organic Letters 10 (20), 4609-4612, 2008 | 66 | 2008 |
| Synthesis and enantioseparation of chiral Au 13 nanoclusters protected by bis-N-heterocyclic carbene ligands H Yi, KM Osten, TI Levchenko, AJ Veinot, Y Aramaki, T Ooi, M Nambo, ... Chemical Science 12 (31), 10436-10440, 2021 | 54 | 2021 |
| Pd-catalyzed desulfonative cross-coupling of benzylic sulfone derivatives with 1, 3-oxazoles JCH Yim, M Nambo, CM Crudden Organic letters 19 (14), 3715-3718, 2017 | 54 | 2017 |
| Palladium‐Catalyzed Carbon–Carbon Bond Formation and Cleavage of Organo (hydro) fullerenes M Nambo, K Itami Chemistry–A European Journal 15 (19), 4760-4764, 2009 | 53 | 2009 |
| Desulfonylative transformations of sulfones by transition-metal catalysis, photocatalysis, and organocatalysis M Nambo, Y Maekawa, CM Crudden ACS Catalysis 12 (5), 3013-3032, 2022 | 51 | 2022 |
| Modular synthesis of α-fluorinated arylmethanes via desulfonylative cross-coupling M Nambo, JCH Yim, LBO Freitas, Y Tahara, ZT Ariki, Y Maekawa, ... Nature Communications 10 (1), 4528, 2019 | 46 | 2019 |
| Synthesis and Characterization of Enantiopure Chiral Bis NHC-Stabilized Edge-Shared Au10 Nanocluster with Unique Prolate Shape RWY Man, H Yi, S Malola, S Takano, T Tsukuda, H Häkkinen, M Nambo, ... Journal of the American Chemical Society 144 (5), 2056-2061, 2022 | 42 | 2022 |
