| Site-specific modification of amino acids and peptides by aldehyde–alkyne–amine coupling under ambient aqueous conditions N Uhlig, CJ Li Organic letters 14 (12), 3000-3003, 2012 | 62 | 2012 |
| Gold-catalyzed tandem reactions of amide–aldehyde–alkyne coupling and cyclization-synthesis of 2, 4, 5-trisubstituted oxazoles P Querard, SA Girard, N Uhlig, CJ Li Chemical Science 6 (12), 7332-7335, 2015 | 47 | 2015 |
| Alkynes as an eco-compatible “on-call” functionality orthogonal to biological conditions in water N Uhlig, CJ Li Chemical Science 2 (7), 1241-1249, 2011 | 44 | 2011 |
| Aniline Carbamates: A Versatile and Removable Motif for Palladium‐Catalyzed Directed C H Activation N Uhlig, CJ Li Chemistry–A European Journal 20 (38), 12066-12070, 2014 | 41 | 2014 |
| Combined A3 Coupling and Click Chemistry Approach for the Synthesis of Dendrimer-Based Biological Tools A Sharma, D Mejía, A Regnaud, N Uhlig, CJ Li, D Maysinger, A Kakkar ACS Macro Letters 3 (10), 1079-1083, 2014 | 24 | 2014 |
| Selective DIBAL-H monoreduction of a diester using continuous flow chemistry: from benchtop to kilo Lab N Uhlig, A Martins, D Gao Organic Process Research & Development 24 (10), 2326-2335, 2020 | 14 | 2020 |
| Catalytic Nucleophilic Addition of Alkynes to Imines: The A3 (Aldehyde–Alkyne–Amine) Coupling N Uhlig, WJ Yoo, L Zhao, CJ Li Modern Alkyne Chemistry: Catalytic and Atom‐Economic Transformations, 239-268, 2014 | 14* | 2014 |
| Methods of preparing 1′-cyano nucleosides PR Badalov, S Bremner, MR Chin, D Gao, N Griggs, LV Heumann, C Lai, ... US Patent 11,613,553, 2023 | 13 | 2023 |
| Synthesis of 2, 5-Disubstituted Oxazoles from Arylacetylenes and α-Amino Acids through an I2/Cu (NO3) 2• 3H2O-Assisted Domino Sequence J Wang, Y Cheng, J Xiang, A Wu Synlett 30 (06), 743-747, 2019 | 9 | 2019 |
| Microwave-assisted CuCl-catalyzed three-component reactions of alkynes, aldehydes, and amino alcohols X Li, N Chen, J Xu Synthesis 51 (17), 3336-3344, 2019 | 7 | 2019 |
| Make mine nearly neat: Aqueous and high-concentration reactions for selective carbon-carbon bond formation N Uhlig McGill University, 2015 | 1 | 2015 |
| Methods of preparing 1-cyano nucleosides PR Badalov, S Bremner, MR Chin, D Gao, N Griggs, LV Heumann, C Lai, ... US Patent App. 18/108,480, 2023 | | 2023 |
| Flow Chemistry As an Enabling Tool for Scale-up of API Processes D Gao, T Vieira, A Stevens, N Uhlig, A Martins, L Heumann, ... 2022 AIChE Annual Meeting, 2022 | | 2022 |
| Methods of preparing 1'-cyano nucleosides Todd A. Wenderski, Pavel R. Badalov, Stacy Bremner, Matthew R. Chin, Detian ... WO Patent WO/2021/183,750, 2021 | | 2021 |
| Selective Monoreduction of a Pyridine Diester on a Kilogram Scale N UHLIG, A MARTINS, D GAO | | 2020 |
Chao-Jun LiMcGill Univ, Tulane Univ, Stanford UnivПідтверджена електронна адреса в mcgill.ca
