Publications
Ferrocene-Containing DNA Monolayers: Influence of Electrostatics on the Electron Transfer Dynamics. Langmuir : the ACS journal of surfaces and colloids 2021, 37 (11), 3359-3369.
Fe-Catalyzed reactions of 2-chloro-1,7-dienes and allylmalonates. Tetrahedron Letters 2007, 48 (26), 4539-4541 DOI: 10.1016/j.tetlet.2007.04.143.
Extension of the Library of Biologically Active γ-Alkylidene Butenolides. Synthesis 2008, 2008 (21), 3465-3472 DOI: 10.1055/s-0028-1083181.
Extending molecular dynamics with dipolar NMR tensors as constraints to chiral phosphorus compounds. Physical Chemistry Chemical Physics 2024, 26 (31), 20814-20819.
Exploring the "Goldilocks Zone" of Semiconducting Polymer Photocatalysts by Donor-Acceptor Interactions. Angewandte Chemie-International Edition 2018, 57 (43), 14188-14192 DOI: 10.1002/anie.201809702.
Exploring Supramolecular Gels in Flow-Type Chemistry-Design and Preparation of Stationary Phases. Industrial and Engineering Chemistry Research 2021, 60 (28), 10056-10063.
Exploring positions 6 and 7 of a quinazoline-based scaffold leads to changes in selectivity and potency towards RIPK2/3 kinases. European Journal of Medicinal Chemistry 2023, 260 (November).
Exploring long-range fluorine-carbon J-coupling for conformational analysis of deoxyfluorinated disaccharides: A combined computational and NMR study. Bioorganic Chemistry 2024, 147 (JUN 2024).
Experimentally Calibrated Analysis of the Electronic Structure of CuO+: Implications for Reactivity. Angewandte Chemie-International Edition 2018, 57 (52), 17053-17057 DOI: 10.1002/anie.201811362.
Expedient production of site specifically nucleobase-labelled or hypermodified RNA with engineered thermophilic DNA polymerases. Nature Communications 2024, 15 (1).
Expedient production of site specifically nucleobase-labelled or hypermodified RNA with engineered thermophilic DNA polymerases (vol 15, 3054, 2023). Nature Communications 2024, 15 (1).
Exfoliation of Crystalline 2D Carbon Nitride: Thin Sheets, Scrolls and Bundles via Mechanical and Chemical Routes. Macromolecular Rapid Communications 2013, 34 (10), 850-854 DOI: 10.1002/marc.201300086.
Exclusive Papers of the Editorial Board Members and Topical Advisory Panel Members of Catalysts in Section "Catalysis in Organic and Polymer Chemistry". Catalysts 2024, 14 (7).
Examination of small molecule losses in 5-methylpyranopelargonidin MS/MS CID spectra by DFT calculations: MS/MS and DFT of 5-methylpyranopelargonidin. Journal of Mass Spectrometry 2014, 49 (12), 1314-1321 DOI: 10.1002/jms.3466.
Evidence for the Cyclic CN 2 Carbene in the Gas Phase. Organic Letters 2014, 16 (20), 5482-5485 DOI: 10.1021/ol5027602.
Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide. Organic Letters 2016, 18 (21), 5656-5659 DOI: 10.1021/acs.orglett.6b02897.
Enantioselective synthesis of spiroimidazolones by synergistic catalysis. Catalysis Today 2024, 428 (February).
Enantioselective Synthesis of Spiro Heterocyclic Compounds Using a Combination of Organocatalysis and Transition-Metal Catalysis. Chemical Record 2023, 23 (7).
Enantioselective Synthesis of (-)-Methoxyestrone. European Journal of Organic Chemistry 2011, 2011 (18), 3279-3282 DOI: 10.1002/ejoc.201100317.
Enantioselective Synthesis of All-Carbon Quaternary Centers Structurally Related to Amaryllidaceae Alkaloids. Chemistry-a European Journal 2018, 24 (40), 10069-10072 DOI: 10.1002/chem.201802493.
Enantioselective PCCP Brønsted acid-catalyzed aminalization of aldehydes. Beilstein Journal of Organic Chemistry 2021, 17 (September), 2433-2440.
Enantioselective Organocatalytic Synthesis of Sulfur-Containing Spirocyclic Compounds: Organocatalytic Synthesis of Sulfur-Containing Spiro Compounds. European Journal of Organic Chemistry 2013, 2013 (35), 7979-7988 DOI: 10.1002/ejoc.201300931.
Enantioselective Organocatalytic Synthesis of 1,2,3-Trisubstituted Cyclopentanes. European Journal of Organic Chemistry 2021, 2021 (36), 5080-5089.
Enantioselective Organocatalytic Amination of Pyrazolones. Asian Journal of Organic Chemistry 2013, 2 (1), 64-68 DOI: 10.1002/ajoc.201200168.
Enantioselective methodologies using N-carbamoyl-imines. Chem. Soc. Rev. 2014, 43 (2), 611-630 DOI: 10.1039/C3CS60321K.