Publications
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Influence of substituent position and cavity size of the regioisomers of monocarboxymethyl-α-, β-, and γ-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Tröger's base. Journal of Separation Science 2016, 39 (5), 980-985 DOI: 10.1002/jssc.201500845.
Influence of substituent position and cavity size of the regioisomers of monocarboxymethyl-α-, β-, and γ-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Tröger's base. Journal of Separation Science 2016, 39 (5), 980-985 DOI: 10.1002/jssc.201500845.
Influence of substituent position and cavity size of the regioisomers of monocarboxymethyl-α-, β-, and γ-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Tröger's base. Journal of Separation Science 2016, 39 (5), 980-985 DOI: 10.1002/jssc.201500845.
Interaction of Ruthenium(II) with Terminal Alkynes: Benchmarking DFT Methods with Spectroscopic Data. Organometallics 2016, 35 (7), 990-994 DOI: 10.1021/acs.organomet.6b00021.
Kinetic, thermodynamic and structural analysis of tamiphosphor binding to neuraminidase of H1N1 (2009) pandemic influenza. European Journal of Medicinal Chemistry 2016, 121, 100-109 DOI: 10.1016/j.ejmech.2016.05.016.
Magnetic Circular Dichroism Evidence for an Unusual Electronic Structure of a Tetracarbene–Oxoiron(IV) Complex. Journal of the American Chemical Society 2016, 138 (43), 14312-14325 DOI: 10.1021/jacs.6b07708.
Solvatochromic fluorene-linked nucleoside and DNA as color-changing fluorescent probes for sensing interactions. Chem. Sci. 2016, 7 (9), 5775-5785 DOI: 10.1039/C6SC02548J.
Spectroscopic Characterization and Reactivity of Triplet and Quintet Iron(IV) Oxo Complexes in the Gas Phase. Angewandte Chemie International Edition 2016, 55 (11), 3637-3641 DOI: 10.1002/anie.201511374.
Carboxylate-assisted C–H activation of phenylpyridines with copper, palladium and ruthenium: a mass spectrometry and DFT study. Chem. Sci. 2015, 6 (10), 5544-5553 DOI: 10.1039/C5SC01729G.
Direct One-Pot Synthesis of Nucleosides from Unprotected or 5-O-Monoprotected D-Ribose. Organic Letters 2015, 17 (18), 4604-4607 DOI: 10.1021/acs.orglett.5b02332.
Infrared and Visible Photodissociation Spectra of Rhodamine Ions at 3 K in the Gas Phase. The Journal of Physical Chemistry A 2015, 119 (51), 12648-12655 DOI: 10.1021/acs.jpca.5b08462.
Infrared spectroscopy of CHCl2+ molecular dications. International Journal of Mass Spectrometry 2015, 377, 109-115 DOI: 10.1016/j.ijms.2014.07.001.
Investigation of Geminally Diaurated Arene Complexes in the Gas Phase. Organometallics 2015, 34 (16), 3979-3987 DOI: 10.1021/acs.organomet.5b00343.
Reaction Intermediates Kinetics in Solution Investigated by Electrospray Ionization Mass Spectrometry: Diaurated Complexes. Journal of the American Chemical Society 2015, 137 (42), 13647-13657 DOI: 10.1021/jacs.5b08744.
Two-Color Infrared Predissociation Spectroscopy of C 6 H 6 2+ Isomers Using Helium Tagging. The Journal of Physical Chemistry A 2015, 119 (11), 2532-2542 DOI: 10.1021/jp5088064.
Electrochemical behaviour of 2,4-dinitrophenylhydrazi(o)ne as multi-redox centre DNA label at mercury meniscus modified silver solid amalgam electrode. Electrochimica Acta 2014, 126, 122-131 DOI: 10.1016/j.electacta.2013.09.147.
Enantioselective methodologies using N-carbamoyl-imines. Chem. Soc. Rev. 2014, 43 (2), 611-630 DOI: 10.1039/C3CS60321K.
Evidence for the Cyclic CN 2 Carbene in the Gas Phase. Organic Letters 2014, 16 (20), 5482-5485 DOI: 10.1021/ol5027602.
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.
Formation and stability of calcium complexes of dimethyl sulfoxide in water. International Journal of Mass Spectrometry 2014, 360, 8-14 DOI: 10.1016/j.ijms.2014.01.001.
Gas-phase studies of copper catalyzed aerobic cross coupling of thiol esters and arylboronic acids: REACTION MECHANISMS. Journal of Physical Organic Chemistry 2014, 27 (3), 198-203 DOI: 10.1002/poc.3262.
The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2014, 37 (19), 2779-2784 DOI: 10.1002/jssc.201400604.
The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2014, 37 (19), 2779-2784 DOI: 10.1002/jssc.201400604.
The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2014, 37 (19), 2779-2784 DOI: 10.1002/jssc.201400604.
The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2014, 37 (19), 2779-2784 DOI: 10.1002/jssc.201400604.