B. Berking, D. Karagrigoriou, G. Poulladofonou, D. Wilson, K. Neumann*, chemrxiv-2023-d5d3r

Stronger together: Polymeric sulfur ylides with minimal charge separation open a new generation of antifouling and biofilm preventing materials

K. Gavriel, D. van Doeselaar, D. Geers, K. Neumann*, 2023, chemrxiv-2023-q6vlj

Click’n lock: Rapid exchange between asymmetric tetrazines and thiols enables reversible, chemoselective clicking and on demand locking


(15)         R. Remmers, K. Neumann*, Biomater. Sci., 2023, 11, 1607.   

Reaching new lights: A review on photo-controlled nanomedicines and their in vivo evaluation

(14)         G. Poulladofonou, K. Neumann*, Polymer Chemistry, 2022, 13, 4416.

Poly(sulfur ylides): A new class of zwitterionic polymers with distinct thermal and solution behaviour

Publications at ETH Zurich and Edinburgh University

(13)         K. Neumann, A. Vujinovic, S. Kamara, Andre Zwicky, S. Baldauf, J. Bode, RSC Chemical Biology, 2023, accepted article.

Synthesis of Multi-Module Low Density Lipoprotein Receptor Class A Domains with Acid Labile Cyanopyridiniumylides (CyPY) as Aspartic Acid Masking Groups

(12)         J. Geng, Y. Zhang, Q. Gao, K. Neumann, H. Dong, H. Porter, M. Potter, H. Ren, D. Argyle and M. Bradley, Nature Chemistry, 2021, 13, 805.

Switching on prodrugs using radiotherapy

highlighted in synform: 2022/01, A14–A18.

(11)        D. Schauenburg, M. Divandari, K. Neumann, C. A. Spiegel, T. Hackett, Y. Dzeng, N. D.  Spencer and J. W.  Bode, Angewandte Chemie, 2020, 59, 14656.

Synthesis of polymers containing potassium acyltrifluoroborates (KATs) and post-polymerization ligation and conjugation

(10)        K. Neumann, J. Farnung, S. Baldauf and J. W. Bode, Nature Communication, 2020, 11, 982.

Prevention of aspartimide formation during peptide synthesis using cyanosulfurylides as carboxylic acid-protecting groups

(9)        K. Neumann*, A. Gambardella and M. Bradley*, ChemBioChem, 2019, 7, 872.

The Emerging Role of Tetrazines in Drug-Activation Chemistries

(8)        K. Neumann*, A. Gambardella, A. Lilienkampf and M. Bradley*, Chem. Sci. 2018, 9, 7198.

Tetrazine-mediated bioorthogonal prodrug–prodrug activation

(7)        K. Neumann*, A. Lilienkampf and M. Bradley*, Polym Int, 2017, 66, 1756.

Responsive polymeric nanoparticles for controlled drug delivery

(6)        K. Neumann, A. C. Gonzalez, M. Owens, A. Venturato, Y. Zhang, J. Geng and M. Bradley, Macromolecules, 2017, 50, 6026. 

An Approach to the High-Throughput Fabrication of Glycopolymer Microarrays through Thiol–Ene Chemistry

(5)        X. Feng, G. Wang, K. Neumann, W. Yao, L. Ding, S. Li, Y. Sheng, Y. Jiang, M. Bradley and R. Zhang, Materials Science and Engineering: C, 2017, 74, 270.

Synthesis and characterization of biodegradable poly(ether-ester) urethane acrylates for controlled drug release

(4)        K. Neumann, S. Jain, A. Gambardella, E. Valero, S. E. Walker, A. Lilienkampf and M. Bradley, ChemBioChem, 2017, 18, 91.

Tetrazine‐Responsive Self‐immolative Linkers

ChemBioChem Readers’ Choice – Most Read Articles in 2018 and 2019.

(3)        G. Wang, Z. Duan, Y. Sheng, K. Neumann, L. Deng, J. Li, M. Bradley and R. Zhang, Chem. Commun. 2016, 52, 10521.

Tuning the emission properties of a fluorescent polymer using a polymer microarray approach – identification of an optothermo responsive polymer

(2)     S. JainK. Neumann, Y. Zhang, E. Valero, J. Geng and M. Bradley, Macromolecules, 2016, 49, 5438.

Tetrazine-Mediated Postpolymerization Modification

(1)     K. Neumann, S. Jain, J. Geng and M. Bradley, Chem. Commun., 2016, 52, 11223.

Nanoparticle “switch-on” by tetrazine triggering

© neumann-lab