Supporting Information
Supporting Information File 1: UV spectra for selected macrocycles, additional NMR and MS spectra for all newly synthesized macrocyles. | ||
Format: PDF | Size: 937.2 KB | Download |
Cite the Following Article
Homochiral BINOL-based macrocycles with π-electron-rich, electron-withdrawing or extended spacing units as receptors for C60
Marco Caricato, Silvia Díez González, Idoia Arandia Ariño and Dario Pasini
Beilstein J. Org. Chem. 2014, 10, 1308–1316.
https://doi.org/10.3762/bjoc.10.132
How to Cite
Caricato, M.; González, S. D.; Arandia Ariño, I.; Pasini, D. Beilstein J. Org. Chem. 2014, 10, 1308–1316. doi:10.3762/bjoc.10.132
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
- Kirinda, V. C.; Schrage, B. R.; Ziegler, C. J.; Hartley, C. S. ortho-Phenylene-Based Macrocyclic Hydrocarbons Assembled Using Olefin Metathesis. European Journal of Organic Chemistry 2020, 2020, 5620–5625. doi:10.1002/ejoc.202000950
- Sun, M.; Xu, L.; Pan, F.; Xiaoling, W.; Kuang, H.; Liu, L.; Xu, C. Scissor-Like Chiral Metamolecules for Probing Intracellular Telomerase Activity. Advanced Functional Materials 2016, 26, 7352–7358. doi:10.1002/adfm.201601942
- Pasini, D.; Nitti, A. Recent Advances in Sensing Using Atropoisomeric Molecular Receptors. Chirality 2015, 28, 116–123. doi:10.1002/chir.22556
- Caricato, M.; Delforge, A.; Bonifazi, D.; Dondi, D.; Mazzanti, A.; Pasini, D. Chiral nanostructuring of multivalent macrocycles in solution and on surfaces. Organic & biomolecular chemistry 2015, 13, 3593–3601. doi:10.1039/c4ob02643h
- Coluccini, C.; Caricato, M.; Cariati, E.; Righetto, S.; Forni, A.; Pasini, D. Synthesis, chiroptical and SHG properties of polarizable push–pull dyes built on π-extended binaphthyls. RSC Advances 2015, 5, 21495–21503. doi:10.1039/c4ra16876c