Supporting Information
| Supporting Information File 1: Experimental procedures, characterization data, copies of NMR spectra and chiral HPLC analysis. | ||
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| Supporting Information File 2: 2D NMR spectra of compounds 4a–d and 5a–d. | ||
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| Supporting Information File 3: 2D NMR spectra of compounds 8a–d, 9a–d and 11. | ||
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Cite the Following Article
New α- and β-cyclodextrin derivatives with cinchona alkaloids used in asymmetric organocatalytic reactions
Iveta Chena Tichá, Simona Hybelbauerová and Jindřich Jindřich
Beilstein J. Org. Chem. 2019, 15, 830–839.
https://doi.org/10.3762/bjoc.15.80
How to Cite
Tichá, I. C.; Hybelbauerová, S.; Jindřich, J. Beilstein J. Org. Chem. 2019, 15, 830–839. doi:10.3762/bjoc.15.80
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- Noël, S.; Caronia, E.; Bricout, H.; Tichá, I.; Menuel, S.; Ponchel, A.; Tilloy, S.; Galia, A.; Monflier, E.; Jindřich, J.; Léger, B. Asymmetric hydrogenation of ethyl pyruvate over aqueous dispersed Pt nanoparticles stabilized by a cinchonidine-functionalized β-cyclodextrin. Catalysis Communications 2021, 150, 106272. doi:10.1016/j.catcom.2020.106272
- Tichá, I.; Benkovics, G.; Malanga, M.; Jindřich, J. Enhanced single-isomer separation and pseudoenantiomer resolution of new primary rim heterobifunctionalized α-cyclodextrin derivatives. Beilstein journal of organic chemistry 2018, 14, 2829–2837. doi:10.3762/bjoc.14.261
