Supporting Information
| Supporting Information File 1: Experimental details and characterisation data (including X-ray data for 4a, 7a, and 7d, NMR, IR, and HRMS) as well as NMR titration data. | ||
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Cite the Following Article
Chiral anion recognition using calix[4]arene-based ureido receptors in a 1,3-alternate conformation
Tereza Horáčková, Jan Budka, Vaclav Eigner, Wen-Sheng Chung, Petra Cuřínová and Pavel Lhoták
Beilstein J. Org. Chem. 2020, 16, 2999–3007.
https://doi.org/10.3762/bjoc.16.249
How to Cite
Horáčková, T.; Budka, J.; Eigner, V.; Chung, W.-S.; Cuřínová, P.; Lhoták, P. Beilstein J. Org. Chem. 2020, 16, 2999–3007. doi:10.3762/bjoc.16.249
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Scholarly Works
- Yesypenko, O. A.; Trybrat, O. O.; Karpichev, Y. A.; I. Kalchenko, V. Regioselective Functionalization of the para-Positions at the Calix[4]arene Upper Rim. Current Organic Chemistry 2023, 27, 510–525. doi:10.2174/1385272827666230524120812
- Peluso, P.; Chankvetadze, B. Recognition in the Domain of Molecular Chirality: From Noncovalent Interactions to Separation of Enantiomers. Chemical reviews 2022, 122, 13235–13400. doi:10.1021/acs.chemrev.1c00846
- Karges, J.; Cohen, S. M. Preorganized Homochiral Pyrrole-Based Receptors That Display Enantioselective Anion Binding. European journal of organic chemistry 2022, 2022. doi:10.1002/ejoc.202101346
