Publications

10. Cook, A.; Yadav, P. K.; Wender, P. A. Circular RNA delivery in vitro and in vivo using doubly-branched aminoethoxy-functionalized ionizable lipid nanoparticles. J. Am. Chem Soc. 2026 [accepted].

9. Ives, R. A.; Azulay, D. N.; Cook, A.; Dagar, M.; Fansher, D. J.; Keshari, R.; Ojha, A. A.; Patel, S.; Sandoval-Pauker, C.; Sanghai, N.; Trinh, B. K.; Yadav, V.; Zheng, Z. Reconsidering Excellence in the Chemical Sciences: Lessons from First-Generation Chemists. ACS Cent. Sci., 2026, 12, 1260–1265.

DOI: 10.1021/acscentsci.6c00822

8. Cook, A.; Kassymbek, A.; Vaezghaemi, A.; Barbery, C.; Newman, S. G. An SN1-Approach to Cross-Coupling: Deoxygenative Arylation Facilitated by the β-Silicon Effect. J. Am. Chem. Soc. 2024. 146, 19929–19938.

DOI: 10.1021/jacs.4c03197

7. Cook, A.; Newman, S. G. Alcohols as substrates in transition metal-catalyzed arylation, alkylation and related reactions. Chem. Rev. 2024, 124, 6078–6144.

DOI: 10.1021/acs.chemrev.4c00094

6. Cook, A.; St. Onge, P.; Newman, S. G. Deoxygenative Suzuki-Miyaura Arylation of Tertiary Alcohols Through Silyl Ethers. Nature Synthesis 2023, 2, 663–669.

DOI: 10.1038/s44160-023-00275-w

5. Cook, A.; Bezaire, M.; Newman, S. G. Nickel-Catalyzed Desulfonylative Olefination of β-Hydroxysulfones. Org. Chem. Front., 2023, 10, 1399–1404.

DOI: 10.1039/D2QO01999J

4. St. Onge, P.; Khan, S. I.; Cook, A.; Newman, S. G. Reductive Cleavage of C(sp2)-CF3 Bonds in Trifluoromethylpyridines. Org. Lett., 2023, 25, 1030–1034.

DOI: 10.1021/acs.orglett.3c00258

3. Cook, A.; MacLean, H.; St. Onge, P.; Newman, S. G. Nickel-Catalyzed Reductive Deoxygenation of Diverse C-O Bond-Bearing Functional Groups. ACS Catal., 2021, 11, 13337–13347.

DOI: 10.1021/acscatal.1c03980

2. Cook, A.; Clément, R.; Newman, S. G. Reaction Screening in Multiwell Plates: High-Throughput Optimization of a Buchwald-Hartwig Amination. Nature Protocols 2021, 16, 1152–1169.

DOI: 10.1038/s41596-020-00452-7

1. Cook, A.; Prakash, S.; Zheng, Y.-Z.; Newman, S. G. Exhaustive Reduction of Esters Enabled by Nickel Catalysis. J. Am. Chem. Soc. 2020, 142, 8109–8115.

DOI: 10.1021/jacs.0c02405

science for societal change.