Work

Aryl halide cross-coupling via formate-mediated transfer hydrogenation

Year: 2025

Type: article

Source: Nature Chemistry

DOI: 10.1038/s41557-024-01729-0

Authors: Yoon Cho, Yu-Hsiang Chang, Kevin P. Quirion, Zachary H. Strong, Zachary J. Dubey, Nam Nguyen, Seoyoung Lee, Natalie S. Taylor, Jessica M. Hoover, Nicholas A. White, Peng Liu, Michael J. Krische

Institutions: The University of Texas at Austin, University of Pittsburgh, Genentech, University of Minnesota

Language: English

Topic: Catalytic Cross-Coupling Reactions

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: green

Funders: National Science Foundation, U.S. Department of Health and Human Services, Welch Foundation, National Institutes of Health, National Institute of General Medical Sciences

Awards: MRI: Acquisition of a MALDI-TOF/TOF Mass Spectrometer for Molecular Structure Determination and Imaging, G1309160875, G3046638035, G3277079756, G4253020724, Upgrade of a 500 MHz NMR Spectrometer for Applications in Biomedical Research, Category I. Computing without Boundaries: Cyberinfrastructure for the Long Tail of Science, Computational Models for Reactivity and Selectivity in Transition Metal-Catalyzed Olefin Functionalization, MRI: Acquisition of Cutting-Edge GPU and MPI Nodes for the Interdisciplinary Pitt Center for Research Computing, Understanding Coupling Reactions of Heteroaryls, G5652751621, Catalytic C-C Bond Forming Hydrogenations, Category I: Bridges-2: Scalable Converged Computing, Data, and Analytics for Rapidly Evolving Science and Engineering Research, G781475104, G7991472476, G9000044859

OpenAlex ID: W4408341882

FWCI: 3.47

Cites: 76

Cited by: 12

Related to: 10