L.-C. Campeau
Affiliations: | 2007- | Process Chemistry | Merck & Co., Inc. |
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Publications
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Muir G, Caballero-García G, Muilu T, et al. (2025) Unmasking the halide effect in diastereoselective Grignard reactions applied to C4´ modified nucleoside synthesis. Nature Communications. 16: 1679 |
Lucas C, Fung E, Nodwell M, et al. (2024) A flexible and scalable synthesis of 4'-thionucleosides. Chemical Science |
Michel NWM, Gabbey AL, Edjoc RK, et al. (2024) Nickel-Catalyzed Reductive Arylation of Redox Active Esters for the Synthesis of α-Aryl Nitriles: Investigation of a Chlorosilane Additive. The Journal of Organic Chemistry |
Davison EK, Petrone DA, Meanwell M, et al. (2022) Practical and concise synthesis of nucleoside analogs. Nature Protocols |
Gabbey AL, Michel NWM, Hughes JME, et al. (2022) Synthesis of α-Aryl Secondary Amides via Nickel-Catalyzed Reductive Coupling of Redox-Active Esters. Organic Letters |
Meanwell M, Fehr G, Ren W, et al. (2021) Diversity-oriented synthesis of glycomimetics. Communications Chemistry. 4: 96 |
Piou T, Campeau LC. (2021) Bringing amines back into aziridination. Nature Chemistry. 13: 1027-1028 |
Klapars A, Chung JYL, Limanto J, et al. (2021) Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods. Chemical Science. 12: 9031-9036 |
Meanwell M, Silverman SM, Lehmann J, et al. (2020) A short de novo synthesis of nucleoside analogs. Science (New York, N.Y.). 369: 725-730 |
Campeau LC, Hazari N. (2019) Cross-Coupling and Related Reactions: Connecting Past Success to the Development of New Reactions for the Future. Organometallics. 38: 3-35 |