Design, synthesis and photochemical properties of the first examples of iminosugar clusters based on fluorescent cores

Scholarly Works

• Bonnard, M.; Pinet, S.; Chabaud, L.; Pucheault, M. Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne [3+2]‐Cycloaddition Reaction. European Journal of Organic Chemistry 2024. doi:10.1002/ejoc.202400580
• Compain, P. From Sweet Molecular Giants to Square Sugars and Vice Versa. Synlett 2023, 34, 1866–1893. doi:10.1055/s-0042-1751449
• Zong, X.; Dahiya, H.; Song, Y.; Liang, X.; Pandey, S. K.; Xu, H.; Sharma, G. D. Alkynyl BODIPY-Core Bridged Perylene Diimide Star-Shaped Nonfullerene Acceptors for Efficient Polymer Solar Cells. ACS Applied Energy Materials 2022, 5, 15624–15637. doi:10.1021/acsaem.2c03200
• Barattucci, A.; Gangemi, C. M. A.; Santoro, A.; Campagna, S.; Puntoriero, F.; Bonaccorsi, P. Bodipy-carbohydrate systems: synthesis and bio-applications. Organic & biomolecular chemistry 2022, 20, 2742–2763. doi:10.1039/d1ob02459k
• Gómez, A. M.; Lopez, J. C. Bringing Color to Sugars: The Chemical Assembly of Carbohydrates to BODIPY Dyes. Chemical record (New York, N.Y.) 2021, 21, 3112–3130. doi:10.1002/tcr.202100190
• Agrahari, A. K.; Bose, P.; Jaiswal, M. K.; Rajkhowa, S.; Singh, A. S.; Hotha, S.; Mishra, N.; Tiwari, V. K. Cu(I)-Catalyzed Click Chemistry in Glycoscience and Their Diverse Applications. Chemical reviews 2021, 121, 7638–7956. doi:10.1021/acs.chemrev.0c00920
• Ansteatt, S.; Meares, A.; Ptaszek, M. Amphiphilic Near-IR-Emitting 3,5-Bis(2-Pyrrolylethenyl)BODIPY Derivatives: Synthesis, Characterization, and Comparison with Other (Hetero)Arylethenyl-Substituted BODIPYs. The Journal of organic chemistry 2021, 86, 8755–8765. doi:10.1021/acs.joc.1c00586
• Biagiotti, G.; Purić, E.; Urbančič, I.; Krišelj, A.; Weiss, M.; Mravljak, J.; Gellini, C.; Lay, L.; Chiodo, F.; Anderluh, M.; Cicchi, S.; Richichi, B. Combining cross-coupling reaction and Knoevenagel condensation in the synthesis of glyco-BODIPY probes for DC-SIGN super-resolution bioimaging. Bioorganic chemistry 2021, 109, 104730. doi:10.1016/j.bioorg.2021.104730
• Mora, A. K.; Murudkar, S.; Shivran, N.; Mula, S.; Chattopadhyay, S.; Nath, S. Monitoring the formation of insulin oligomers using a NIR emitting glucose-conjugated BODIPY dye. International journal of biological macromolecules 2020, 166, 1121–1130. doi:10.1016/j.ijbiomac.2020.10.267
• Thomas, B.; Yan, K.-C.; Hu, X.-L.; Donnier-Maréchal, M.; Chen, G.-R.; He, X.-P.; Vidal, S. Fluorescent glycoconjugates and their applications. Chemical Society reviews 2020, 49, 593–641. doi:10.1039/c8cs00118a
• Bozdemir, Ö. A.; Al‐Sharif, H. H. T.; McFarlane, W.; Waddell, P. G.; Benniston, A. C.; Harriman, A. Solid-State Emission from Mono- and Bichromophoric Boron Dipyrromethene (BODIPY) Derivatives and Comparison with Fluid Solution. Chemistry (Weinheim an der Bergstrasse, Germany) 2019, 25, 15634–15645. doi:10.1002/chem.201903902
• Blázquez-Moraleja, A.; Álvarez-Fernández, D.; Montero, R. P.; García-Moreno, I.; Martínez-Martínez, V.; Bañuelos, J.; Sáenz-de-Santa-María, I.; Chiara, M. D.; Chiara, J. L. A general modular approach for the solubility tagging of BODIPY dyes. Dyes and Pigments 2019, 170, 107545. doi:10.1016/j.dyepig.2019.107545
• Bilska-Markowska, M.; Szwajca, A.; Marciniak, B. Design, properties and applications of fluorinated and fluoroalkylated N-containing monosaccharides and their analogues. Journal of Fluorine Chemistry 2019, 227, 109364. doi:10.1016/j.jfluchem.2019.109364
• Avellanal-Zaballa, E.; Ventura, J.; Gartzia-Rivero, L.; Bañuelos, J.; García-Moreno, I.; Uriel, C.; Gómez, A. M.; Lopez, J. C. Towards Efficient and Photostable Red‐Emitting Photonic Materials Based on Symmetric all‐BODIPY‐Triads, ‐Pentads, and ‐Hexads. Chemistry (Weinheim an der Bergstrasse, Germany) 2019, 25, 14959–14971. doi:10.1002/chem.201903804
• Bonacorso, H. G.; Calheiro, T. P.; Acunha, T. V.; Iglesias, B. A.; Franceschini, S. Z.; Ketzer, A.; Meyer, A. R.; Nogara, P. A.; Rocha, J.; Zanatta, N.; Martins, M. A. P. Novel aryl(heteroaryl)-substituted (pyrimidyl)benzamide-based BF2 complexes: Synthesis, photophysical properties, BSA-binding, and molecular docking analysis. Dyes and Pigments 2019, 161, 396–402. doi:10.1016/j.dyepig.2018.09.076
• Donnier-Maréchal, M.; Abdullayev, S.; Bauduin, M.; Pascal, Y.; Fu, M.-Q.; He, X.-P.; Gillon, E.; Imberty, A.; Kipnis, E.; Dessein, R.; Vidal, S. Tetraphenylethylene-based glycoclusters with aggregation-induced emission (AIE) properties as high-affinity ligands of bacterial lectins. Organic & biomolecular chemistry 2018, 16, 8804–8809. doi:10.1039/c8ob02035c
• Nierengarten, J.-F.; Schneider, J. P.; Trinh, T. M. N.; Joosten, A.; Holler, M.; Lepage, M. L.; Bodlenner, A.; García-Moreno, M. I.; Mellet, C. O.; Compain, P. Giant Glycosidase Inhibitors: First- and Second-Generation Fullerodendrimers with a Dense Iminosugar Shell. Chemistry (Weinheim an der Bergstrasse, Germany) 2018, 24, 2483–2492. doi:10.1002/chem.201705600
• Meares, A.; Satraitis, A.; Akhigbe, J.; Santhanam, N.; Swaminathan, S.; Ehudin, M. A.; Ptaszek, M. Amphiphilic BODIPY-Hydroporphyrin Energy Transfer Arrays with Broadly Tunable Absorption and Deep Red/Near-Infrared Emission in Aqueous Micelles. The Journal of organic chemistry 2017, 82, 6054–6070. doi:10.1021/acs.joc.7b00357
• Hatano, A.; Kanno, Y.; Kondo, Y.; Sunaga, Y.; Umezawa, H.; Okada, M.; Yamada, H.; Iwaki, R.; Kato, A.; Fukui, K. Synthesis and characterization of novel, conjugated, fluorescent DNJ derivatives for α-glucosidase recognition. Bioorganic & medicinal chemistry 2016, 25, 773–778. doi:10.1016/j.bmc.2016.11.053
• Dosekova, E.; Filip, J.; Bertok, T.; Both, P.; Kasak, P.; Tkac, J. Nanotechnology in Glycomics: Applications in Diagnostics, Therapy, Imaging, and Separation Processes. Medicinal research reviews 2016, 37, 514–626. doi:10.1002/med.21420

Explore citations to this article at