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Benzene Tetraamide: A Covalent Supramolecular Dual Motif in Dynamic Covalent Polymer Networks

H. Zhang, A. van Hertrooij, T. Schnitzer, Y. Chen, S. Majumdar, R.A.T.M. van Benthem, R.P. Sijbesma,* J.P.A. Heuts*

Macromolecules 2023, 56, 16, 6452-6460.


Temperature Direct the Majority-Rules Principle in Supramolecular Copolymers Driven by Triazine-Brenzene Interactions

S.A.H. Jansen,⁺ H. Su,⁺ T. Schnitzer, G. Vantomme, E.W. Meijer*

Chem. Eur. J. 2023, e202301726.


Controlling Helical Asymmetry in Supramolecular Copolymers by In Situ Chemical Modification

F.V. de Graaf, S.A.H. Jansen, T. Schnitzer, E.W. Meijer,* G. Vantomme*

J. Am. Chem. Soc. 2023, 145, 14379–14386.


Crystal Structure Analysis of N-Acetylated Proline and Ring Size Analogs

T. Schnitzer, N. Trapp, L.-M. Fischer, H. Wennemers*

J. Pept. Sci. 2023, e3473.


How Subtle Changes Can Make a Difference: Reproducibility in Complex Supramolecular Systems

T. Schnitzer,⁺ M.D. Preuss,⁺ J. van Basten, S.M.C. Schoenmakers, A.J.H. Spiering, G. Vantomme, E.W. Meijer*

Angew. Chem. Int. Ed. 2022, 61, e202206738.


In-Situ Synthesis of Supramolecular Polymers: Finding the Right Conditions when Combining Covalent and Non-Covalent Synthesis

T. Schnitzer, S.A.H. Jansen, M.F.J. Mabesoone, G. Vantomme, E.W. Meijer*

Angew. Chem. Int. Ed. 2022, 61, e202206729.


Stereoselective Peptide Catalysis in Complex Environments – From River Water to Cell Lysates

T. Schnitzer, J.W. Rackl, H. Wennemers*

Chem. Sci. 2022, 13, 8963-8967.


Efficient Synthesis of Dipyrrolobenzenes and Dipyrrolopyrazines via Bidirectional Gold-Catalysis – A Combined Synthetic and Photophysical Study

R. Heckershoff,⁺ T. Schnitzer,⁺ T. Diederich, L. Eberle, P. Krämer, F. Rominger, M. Rudolph, A.S.K. Hashmi*

J. Am. Chem. Soc. 2022, 144, 8306–8316.


Unravelling the Complexity of Supramolecular Copolymerization Dictated by Triazine-Benzene Interactions

H. Su, S.A.H. Jansen, T. Schnitzer, E. Weyandt, A.T. Rösch, J. Liu, G. Vantomme, E.W. Meijer*

J. Am. Chem. Soc. 2021, 143, 17128–17135.


Rotational Isomerism of an Amide Substituted Squaraine Dye – A Combined Spectroscopic and Computational Study

A.T. Rösch, S.H.M. Söntjes, J. Robben, A.R.A. Palmans, T. Schnitzer*

J. Org. Chem. 2021, 86, 13100–13103.


Oligodimethylsiloxane-Oligoproline Block Co-Oligomers: the Interplay between Aggregation and Phase Segregation in Bulk and Solution

B.A.G. Lamers, A. Herlitschka, T. Schnitzer, M.F.J. Mabesoone, S.M.C. Schoenmakers, B.F.M. de Waal, A.R.A. Palmans, H. Wennemers,* E.W. Meijer*

J. Am. Chem. Soc. 2021, 143, 4032–4042.


Peptide-Metal Frameworks with Metal Strings Guided by Dispersion Interactions

T. Schnitzer, E. Paenurk, N. Trapp, R. Gershoni-Poranne, H. Wennemers*

J. Am. Chem. Soc. 2021, 143, 644–648.


Synthesis of Complex Molecular Systems – The Foreseen Role of Organic Chemists

T. Schnitzer,* G. Vantomme*

ACS Cent. Sci. 2020, 6, 2060–2070.


Deactivation of Secondary Amine Catalysts via Aldol Reaction – Amine Catalysis under Solvent-Free Conditions

T. Schnitzer, H. Wennemers*

J. Org. Chem. 2020, 85, 7633–7640.


Amine Catalysis with Substrates Bearing N‐Heterocyclic Moieties Enabled by Control over the Enamine Pyramidalization Direction

J.S. Möhler,⁺ T. Schnitzer,⁺ H. Wennemers*

Chem. Eur. J. 2020, 26, 15623–15628.


Impact of the 𝛽-Turn Hydrogen Bond in the Trans/Cis Ratio and the Performance of the Peptide Catalyst H-DPro-Pro-Glu-NH₂

T. Schnitzer,* R.L. Ganzoni, H. Wennemers*

Tetrahedron 2020, 76, 131184–131188.


Organocatalysed Conjugate Addition Reactions of Aldehydes to Nitroolefins with Anti Selectivity

T. Schnitzer, A. Budinska, H. Wennemers*

Nat. Catal. 2020, 3, 143–147.


Effect of the Enamine Pyramidalization Direction on the Reactivity of Secondary Amine Organocatalysts

T. Schnitzer,⁺ J.S. Möhler,⁺ H. Wennemers*

Chem. Sci. 2020, 11, 1943–1947.


Why Proline? Influence of Ring Size on the Collagen Triple Helix

J. Egli,⁺ T. Schnitzer,⁺ J. Dietschreit, C. Ochsenfeld, H. Wennemers*

Org. Lett. 2020, 22, 348–351.


Effect of 𝛽³-Amino Acids on the Performance of the Peptidic Catalyst H-DPro-Pro-Glu-NH₂

T. Schnitzer, H. Wennemers*

Helv. Chim. Acta 2019, 102, e1900070.


Effect of 𝛾-substituted Proline Derivatives on the Performance of the Peptidic Catalyst H-DPro-Pro-Glu-NH₂

T. Schnitzer, H. Wennemers*

Synthesis 2018, 22, 4377–4382.


Influence of the trans/cis Conformer Ratio on the Stereoselectivity of Peptidic Catalysts

T. Schnitzer, H. Wennemers*

J. Am. Chem. Soc. 2017, 139, 15356–15362.


Is More Better? A Comparison of Tri- and Tetrapeptidic Catalysts

T. Schnitzer, M. Wiesner, P. Krattiger, J. D. Revell, H. Wennemers*

Org. Biomol. Chem. 2017, 15, 5877– 5881.


A Stereoselective Tripeptide Catalyst for Conjugate Addition Reactions of Acetophenones to Dicyanoolefins

T. Schnitzer, H. Wennemers*

Synlett 2017, 28, 1282–1286.


Addition of Organometallic Reagents to Chiral N-Methoxylactams: Enantioselective Syntheses of Pyrrolidines and Piperidines

M. Jäkel, J. Qu, T. Schnitzer, G. Helmchen*

Chem. Eur. J. 2013, 19, 16746–16755.

⁺ authors contributed equally, * corresponding author

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