Cite the Following Article
Enantioselective supramolecular devices in the gas phase. Resorcin[4]arene as a model system
Caterina Fraschetti, Matthias C. Letzel, Antonello Filippi, Maurizio Speranza and Jochen Mattay
Beilstein J. Org. Chem. 2012, 8, 539–550.
https://doi.org/10.3762/bjoc.8.62
How to Cite
Fraschetti, C.; Letzel, M. C.; Filippi, A.; Speranza, M.; Mattay, J. Beilstein J. Org. Chem. 2012, 8, 539–550. doi:10.3762/bjoc.8.62
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Fraschetti, C.; Letzel, M. C.; Paletta, M.; Mattay, J.; Crestoni, M. E.; Chiavarino, B.; Filippi, A. Unprotected Galactosamine as a Dynamic Key for a Cyclochiral Lock. Journal of the American Society for Mass Spectrometry 2021, 32, 736–743. doi:10.1021/jasms.0c00437
- Chen, X.; Kang, Y.; Zeng, S. Analysis of stereoisomers of chiral drug by mass spectrometry. Chirality 2018, 30, 609–618. doi:10.1002/chir.22833
- Nolting, D.; Malek, R.; Makarov, A. Ion traps in modern mass spectrometry. Mass spectrometry reviews 2017, 38, 150–168. doi:10.1002/mas.21549
- Filippi, A.; Fraschetti, C.; Guarcini, L.; Zazza, C.; Ema, T.; Speranza, M. Spectroscopic Discrimination of Diastereomeric Complexes Involving an Axially Chiral Receptor. Chemphyschem : a European journal of chemical physics and physical chemistry 2017, 18, 2475–2481. doi:10.1002/cphc.201700732
- Yu, X.; Yao, Z. Chiral recognition and determination of enantiomeric excess by mass spectrometry: A review. Analytica chimica acta 2017, 968, 1–20. doi:10.1016/j.aca.2017.03.021
- Fraschetti, C.; Montagna, M.; Crestoni, M. E.; Calcaterra, A.; Aiello, F.; Santi, L.; Filippi, A. Kinetic enantioselectivity of a protonated bis(diamido)-bridged basket resorcin[4]arene towards alanine peptides. Organic & biomolecular chemistry 2017, 15, 1183–1189. doi:10.1039/c6ob02734b
- Paletta, M.; Wiegmann, S.; Berke, H.; Mattay, J. Inherently Chiral Resorcin[4]arenes. Comprehensive Supramolecular Chemistry II; Elsevier, 2017; Vol. 3, pp 75–86. doi:10.1016/b978-0-12-409547-2.12510-7
- Deakyne, C.; Adams, J. Computational Studies of Supramolecular Systems: Resorcinarenes and Pyrogallolarenes. Comprehensive Supramolecular Chemistry II; Elsevier, 2017; Vol. 2, pp 303–342. doi:10.1016/b978-0-12-409547-2.12496-5
- Scriba, G. K. E. Chiral recognition in separation science - an update. Journal of chromatography. A 2016, 1467, 56–78. doi:10.1016/j.chroma.2016.05.061
- Reynolds, J. C.; Chew, M. Q.; Martin, H. J.; Stubbs, E. C.; Waters, M. A.; Crotty, S. C.; Silvestre-Gonzalez, V.; Chan, Y.; Thomas, C. L. P.; Page, P. C. B.; Creaser, C. S.; Heaney, H. Gas-phase and solution studies of three resorcin[4]arene derivatives using electrospray time-of-flight mass spectrometry. European journal of mass spectrometry (Chichester, England) 2013, 19, 253–263. doi:10.1255/ejms.1231
- Fraschetti, C.; Filippi, A.; Crestoni, M. E.; Ema, T.; Speranza, M. Multifunctional Macrocyclic Receptors as Templates for Aromatic Amino Acids: A Rare Example of a Highly Selective Multi‐Input Multi‐Output Chemo‐“Logic Gate”. ChemPlusChem 2013, 78, 979–987. doi:10.1002/cplu.201300086
- Fraschetti, C.; Letzel, M. C.; Filippi, A.; Speranza, M.; Mattay, J. Enantioselective Supramolecular Devices in the Gas Phase — Resorcin[4]arene as a Model System. ChemInform 2012, 43. doi:10.1002/chin.201247261