Supporting Information
| Supporting Information File 1: Experimental section, including IR and NMR spectra of the synthesized compounds. | ||
| Format: PDF | Size: 1.6 MB | Download |
Cite the Following Article
New synthetic strategies for xanthene-dye-appended cyclodextrins
Milo Malanga, Andras Darcsi, Mihaly Balint, Gabor Benkovics, Tamas Sohajda and Szabolcs Beni
Beilstein J. Org. Chem. 2016, 12, 537–548.
https://doi.org/10.3762/bjoc.12.53
How to Cite
Malanga, M.; Darcsi, A.; Balint, M.; Benkovics, G.; Sohajda, T.; Beni, S. Beilstein J. Org. Chem. 2016, 12, 537–548. doi:10.3762/bjoc.12.53
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.
Presentation Graphic
| Picture with graphical abstract, title and authors for social media postings and presentations. | ||
| Format: PNG | Size: 362.5 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Soundarapandian, S.; Alexander, A.; Sumohan Pillai, A.; Manikandan, V.; Enoch, I. V. M. V.; Yousuf, S. Differential interaction of Fluorescein-β-cyclodextrin conjugate to quadruplex kit22 DNA: Inclusion of Berberine and modulation of binding. Journal of biomolecular structure & dynamics 2022, 41, 3791–3799. doi:10.1080/07391102.2022.2056508
- Yannakopoulou, K.; Panagiotakis, S.; Saridakis, E. N.; Malanga, M.; Mavridis, I. M. A self-locked β-cyclodextrin-rhodamine B spirolactam with photoswitching properties. Chemistry, an Asian journal 2021, 17, e202101282. doi:10.1002/asia.202101282
- Kasal, P.; Jindřich, J. Mono-6-Substituted Cyclodextrins—Synthesis and Applications. Molecules (Basel, Switzerland) 2021, 26, 5065. doi:10.3390/molecules26165065
- Wright, T.; Karis, D. G.; Millik, S. C.; Tomkovic, T.; Hatzikiriakos, S. G.; Nelson, A.; Wolf, M. O. Photocross-Linked Antimicrobial Amino-Siloxane Elastomers. ACS applied materials & interfaces 2021, 13, 22195–22203. doi:10.1021/acsami.1c02863
- Xu, L.; Xiaohong, L.; Li, Y.; Yin, Z.; Jin, L.; Lu, L.; Qu, J.; Xiao, M. Enzymatic rhamnosylation of anticancer drugs by an α-l-rhamnosidase from Alternaria sp. L1 for cancer-targeting and enzyme-activated prodrug therapy. Applied microbiology and biotechnology 2019, 103, 7997–8008. doi:10.1007/s00253-019-10011-0
- Benkovics, G.; Bálint, M.; Fenyvesi, É.; Varga, E.; Béni, S.; Yannakopoulou, K.; Malanga, M. Homo- and hetero-difunctionalized β-cyclodextrins: Short direct synthesis in gram scale and analysis of regiochemistry. Beilstein journal of organic chemistry 2019, 15, 710–720. doi:10.3762/bjoc.15.66
- Yamanoi, T.; Oda, Y.; Katsuraya, K. NMR determination of concentration-switchable inclusion complex of a β-cyclodextrin derivative carrying a benzene group linked to a C,C -glucopyranoside spacer. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2017, 89, 189–197. doi:10.1007/s10847-017-0746-0
- Thomsen, H.; Benkovics, G.; Fenyvesi, É.; Farewell, A.; Malanga, M.; Ericson, M. B. Delivery of cyclodextrin polymers to bacterial biofilms - An exploratory study using rhodamine labelled cyclodextrins and multiphoton microscopy. International journal of pharmaceutics 2017, 531, 650–657. doi:10.1016/j.ijpharm.2017.06.011
- Benkovics, G.; Malanga, M.; Fenyvesi, É. The ‘Visualized’ macrocycles: Chemistry and application of fluorophore tagged cyclodextrins. International journal of pharmaceutics 2017, 531, 689–700. doi:10.1016/j.ijpharm.2017.04.035
- Benkovics, G.; Afonso, D.; Darcsi, A.; Béni, S.; Conoci, S.; Fenyvesi, É.; Szente, L.; Malanga, M.; Sortino, S. Novel β-cyclodextrin–eosin conjugates. Beilstein journal of organic chemistry 2017, 13, 543–551. doi:10.3762/bjoc.13.52
- Huang, J.; Weinfurter, S.; Pinto, P. C.; Pretze, M.; Kränzlin, B.; Pill, J.; Federica, R.; Perciaccante, R.; Della Ciana, L.; Masereeuw, R.; Gretz, N. Fluorescently Labeled Cyclodextrin Derivatives as Exogenous Markers for Real-Time Transcutaneous Measurement of Renal Function. Bioconjugate chemistry 2016, 27, 2513–2526. doi:10.1021/acs.bioconjchem.6b00452