Researcher Portfolio

Neumann, Constanze N.

Department for Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA, Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States, Research Group Neumann, Max-Planck-Institut für Kohlenforschung, Max Planck Society

Researcher Profile

Position: Research Group Neumann, Max-Planck-Institut für Kohlenforschung, Max Planck Society

Position: Department for Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA

Position: Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States

Researcher ID: https://pure.mpg.de/cone/persons/resource/persons260532

External references

WorldCat Search for Neumann, Constanze N.

Google Scholar Search for Neumann, Constanze N.

Publications

: Bengsch, M., & Neumann, C. N. (2025). Metal-Organic Framework–Specific Catalysis. ChemCatChem, e202402102. doi:10.1002/cctc.202402102. [PubMan] : Jin, Q., Bruzzese, P. C., Vetere, A., Weidenthaler, C., Budiyanto, E., Henglin, M., Nöthling, N., Schnegg, A., & Neumann, C. N. (2024). Programmable Metal Arrangements in Metal-Organic Polyhedra and Frameworks. ChemRxiv: the Preprint Server for Chemistry. doi:10.26434/chemrxiv-2024-h09tl. [PubMan] : Karam, L., Farès, C., Weidenthaler, C., & Neumann, C. N. (2024). Expedited Synthesis of Metal Phosphides Maximizes Dispersion, Air Stability, and Catalytic Performance in Selective Hydrogenation. Angewandte Chemie International Edition, 63(33): e202404292. doi:10.1002/anie.202404292. [PubMan] : Qiu, Z., Deng, H., & Neumann, C. N. (2024). Site-Isolated Rhodium(II) Metalloradicals Catalyze Olefin Hydrofunctionalization. Angewandte Chemie International Edition, 63(18): e202401375. doi:10.1002/anie.202401375. [PubMan] : Qiu, Z., & Neumann, C. N. (2024). Influence of Cage Effects in Directing the Outcome of C–X Bond Forming Reactions. ACS Organic & Inorganic Au, 4(1), 1-25. doi:10.1021/acsorginorgau.3c00044. [PubMan] : Halder, R., Ma, G., Rickmeier, J., McDaniel, J. W., Petzold, R., Neumann, C. N., Murphy, J. M., & Ritter, T. (2023). Deoxyfluorination of phenols for chemoselective ¹⁸F-labeling of peptides. Nature Protocols, 18(11), 3614-3651. doi:10.1038/s41596-023-00890-z. [PubMan] : Gómez-Suárez, A., & Neumann, C. N. (2023). Stereochemistry in All Its Shapes and Forms: The 56^th Bürgenstock Conference. Angewandte Chemie International Edition, 62(39): e202309468. doi:10.1002/anie.202309468. [PubMan] : Qiu, Z., Deng, H., & Neumann, C. N. (2023). Site Isolated Rh(II) Metalloradicals Catalyze Olefin Hydrosilylation. ChemRxiv: the Preprint Server for Chemistry. doi:10.26434/chemrxiv-2023-v3zgd. [PubMan] : Karam, L., & Neumann, C. N. (2022). Heterogeneously Catalyzed Carboxylic Acid Hydrogenation to Alcohols. ChemCatChem, 14(22): e202200953. doi:10.1002/cctc.202200953. [PubMan] : Deng, H., Bengsch, M., Tchorz, N., & Neumann, C. N. (2022). Sterically Controlled Late-Stage Functionalization of Bulky Phosphines. Chemistry – A European Journal, 28(51): e202202074. doi:10.1002/chem.202202074. [PubMan] : Neumann, C. N., Payn, M. T., Rozeveld, S. J., Wu, Z., Zhang, G., Comito, R. J., Miller, J. T., & Dincă, M. (2021). Structural Evolution of MOF-Derived RuCo, A General Catalyst for the Guerbet Reaction. ACS Applied Materials and Interfaces, 13(44), 52113-52124. doi:10.1021/acsami.1c09873. [PubMan] : Payne, M. T., Neumann, C. N., Stavitski, E., & Dincǎ, M. (2021). Complexes of Platinum Group Metals with a Conformationally Locked Scorpionate in a Metal–Organic Framework: An Unusually Close Apical Interaction of Palladium(II). Inorganic Chemistry, 60(16), 11764-11774. doi:10.1021/acs.inorgchem.1c00941. [PubMan] : Neumann, C. N., Rozeveld, S. J., & Dincă, M. (2021). MOF-Derived RuCo Catalyzes the Formation of a Plasticizer Alcohol from Renewable Precursors. ACS Catalysis, 11(14), 8521-8526. doi:10.1021/acscatal.1c01391. [PubMan] : Neumann, C. N., & Ritter, T. (2020). Transition-Metal-Mediated and Transition-Metal-Catalyzed Carbon–Fluorine Bond Formation. In P. A. Evans (Ed.), Organic Reactions (pp. 613). John Wiley and Sons. doi:10.1002/0471264180.or104.03. [PubMan] : Neumann, C. N., Rozeveld, S. J., Yu, M., Rieth, A. J., & Dincă, M. (2019). Metal–Organic Framework-Derived Guerbet Catalyst Effectively Differentiates between Ethanol and Butanol. Journal of the American Chemical Society, 141(44), 17477-17481. doi:10.1021/jacs.9b08968. [PubMan] : Neumann, C. N., & Ritter, T. (2017). Facile C−F Bond Formation through a Concerted Nucleophilic Aromatic Substitution Mediated by the PhenoFluor Reagent. Accounts of Chemical Research, 50(11), 2822-2833. doi:10.1021/acs.accounts.7b00413. [PubMan] : Beyzavi, M. H., Mandal, D., Strebl, M. G., Neumann, C. N., D'Amato, E. M., Chen, J., Hooker, J. M., & Ritter, T. (2017). ¹⁸F‑Deoxyfluorination of Phenols via Ru π‑Complexes. ACS Central Science, 3(9), 944-948. doi:10.1021/acscentsci.7b00195. [PubMan] : Neumann, C. N., & Ritter, T. (2016). C–H fluorination: U can fluorinate unactivated bonds. Nature Chemistry, 8(9), 822-823. doi:10.1038/nchem.2604. [PubMan] : Neumann, C. N., Hooker, J. M., & Ritter, T. (2016). Concerted nucleophilic aromatic substitution with ¹⁹F⁻ and ¹⁸F⁻. Nature, 534(7607), 369-373. doi:10.1038/nature17667. [PubMan] : D'Amato, E. M., Neumann, C. N., & Ritter, T. (2015). Selective Aromatic C-H Hydroxylation Enabled by η⁶-Coordination to Iridium(III). Organometallics, 34(18), 4626-4631. doi:10.1021/acs.organomet.5b00731. [PubMan] : Shen, X., Neumann, C. N., Kleinlein, C., Goldberg, N. W., & Ritter, T. (2015). Alkyl Aryl Ether Bond Formation with PhenoFluor. Angewandte Chemie International Edition, 54(19), 5662-5665. doi:10.1002/anie.201500902. [PubMan] : Neumann, C. N., & Ritter, T. (2015). Late-Stage Fluorination: Fancy Novelty or Useful Tool? Angewandte Chemie International Edition, 54(11), 3216-3221. doi:10.1002/anie.201410288. [PubMan] : Liang, T., Neumann, C. N., & Ritter, T. (2013). Introduction of Fluorine and Fluorine-Containing Functional Groups. Angewandte Chemie International Edition, 52(32), 8214-8264. doi:10.1002/anie.201206566. [PubMan] : Kamlet, A. S., Neumann, C. N., Lee, E., Carlin, S. M., Moseley, C. K., Stephenson, N., Hooker, J. M., & Ritter, T. (2013). Application of Palladium-Mediated ¹⁸F-Fluorination to PET Radiotracer Development: Overcoming Hurdles to Translation. PLoS One, 8(3): e59187. doi:10.1371/journal.pone.0059187. [PubMan] : Lee, E., Kamlet, A. S., Powers, D. C., Neumann, C. N., Boursalian, G. B., Furuya, T., Choi, D. C., Hooker, J. M., & Ritter, T. (2011). A Fluoride-Derived Electrophilic Late-Stage Fluorination Reagent for PET Imaging. Science, 334(6056), 639-642. doi:10.1126/science.1212625. [PubMan]