Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Jordan M. Rabus"'
Autor:
Jordan M. Rabus, Shanshan Guan, Lauren M. Schultz, Maha T. Abutokaikah, Philippe Maître, Benjamin J. Bythell
Publikováno v:
Journal of the American Society for Mass Spectrometry. 33:1745-1752
Autor:
Deva Saroja Talasila, Evan Stephenson, Jordan M. Rabus, Matthew J. Queensen, Kellsie Jurkowski, Eike B. Bauer, Michael Barnes-Flaspoler
Publikováno v:
European Journal of Organic Chemistry. 2019:7348-7358
Publikováno v:
Journal of The American Society for Mass Spectrometry
Journal of The American Society for Mass Spectrometry, Springer Verlag (Germany), 2020, 2020 (2), pp.89-101. ⟨10.1021/jasms.0c00074⟩
Journal of The American Society for Mass Spectrometry, Springer Verlag (Germany), 2020, 2020 (2), pp.89-101. ⟨10.1021/jasms.0c00074⟩
We investigate the structure and dissociation pathways of the deprotonated amphoteric peptide arginylglycylasparic acid, [RGD-H]−. We model the pertinent gas-phase structures and fragmentation chem...
Publikováno v:
Physical Chemistry Chemical Physics. 19:25643-25652
We investigate the gas-phase structures and fragmentation chemistry of two isomeric sodium-cationized carbohydrates using combined tandem mass spectrometry, hydrogen/deuterium exchange experiments, and computational methods. Our model systems are the
Autor:
Jordan M. Rabus, Ashley R. Wagoner, Philippe Maître, Benjamin J. Bythell, Maha T. Abutokaikah
Publikováno v:
Journal of The American Society for Mass Spectrometry
Journal of The American Society for Mass Spectrometry, Springer Verlag (Germany), 2018, 29 (12), pp.2380-2393. ⟨10.1007/s13361-018-2065-0⟩
Journal of The American Society for Mass Spectrometry, Springer Verlag (Germany), 2018, 29 (12), pp.2380-2393. ⟨10.1007/s13361-018-2065-0⟩
We investigate the tandem mass spectrometry of regiospecifically labeled, deprotonated sucrose analytes. We utilize density functional theory calculations to model the pertinent gas-phase fragmentation chemistry of the prevalent glycosidic bond cleav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a87678248152d91fcc94ea66d521f42c
https://hal.archives-ouvertes.fr/hal-02334557
https://hal.archives-ouvertes.fr/hal-02334557
Publikováno v:
Journal of the American Society for Mass Spectrometry. 30(7)
We demonstrate increasing the charge state of small molecules using derivatized lysine as our model system. Lysine is chemically tagged with three tertiary amines which enables efficient production of highly charged analytes. A +3 charge state is obt
Publikováno v:
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2018, 20 (44), pp.27897-27909. ⟨10.1039/c8cp02620c⟩
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2018, 20 (44), pp.27897-27909. ⟨10.1039/c8cp02620c⟩
We investigate the gas-phase structures and fragmentation chemistry of deprotonated carbohydrate anions using combined tandem mass spectrometry, infrared spectroscopy, regioselective labelling, and theory. Our model system is deprotonated, [lactose-H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6e195a547d8930c14971b840289f1a9
https://hal.archives-ouvertes.fr/hal-02334556
https://hal.archives-ouvertes.fr/hal-02334556
Publikováno v:
Journal of the American Society for Mass Spectrometry. 29(8)
We characterize the primary fragmentation reactions of three isomeric lithiated D-hexose sugars (glucose, galactose, and mannose) utilizing tandem mass spectrometry, regiospecific labeling, and theory. We provide evidence that these three isomers pop
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 407:221-229
Commercial ferrocenium hexafluorophosphate ([FeCp 2 ]PF 6 ) was found to be an efficient catalyst for the etherification of terminal, tertiary propargylic alcohols with primary and secondary alcohols (5 h to 3 days reaction time at 40 °C in CH 2 Cl
Publikováno v:
Catalysis Communications. 47:45-48
The cationic ruthenium allenylidene complex R Ru R ax −[Ru(indenyl)L(PPh 3 ) C C CPh 2 ] + PF 6 catalyzes the etherification of secondary and tertiary propargylic alcohols in a formal nucleophilic substitution reaction utilizing primary and seconda