Enabling technologies and green processes in cyclodextrin chemistry

Giancarlo Cravotto, Marina Caporaso, Laszlo Jicsinszky and Katia Martina
Beilstein J. Org. Chem. 2016, 12, 278–294. https://doi.org/10.3762/bjoc.12.30

Cite the Following Article

Enabling technologies and green processes in cyclodextrin chemistry
Giancarlo Cravotto, Marina Caporaso, Laszlo Jicsinszky and Katia Martina
Beilstein J. Org. Chem. 2016, 12, 278–294. https://doi.org/10.3762/bjoc.12.30

How to Cite

Cravotto, G.; Caporaso, M.; Jicsinszky, L.; Martina, K. Beilstein J. Org. Chem. 2016, 12, 278–294. doi:10.3762/bjoc.12.30

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: 583.4 KB Download

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Jicsinszky, L.; Bucciol, F.; Chaji, S.; Cravotto, G. Mechanochemical Degradation of Biopolymers. Molecules (Basel, Switzerland) 2023, 28, 8031. doi:10.3390/molecules28248031
  • Orosz, J. M.; Ujj, D.; Kasal, P.; Benkovics, G.; Bálint, E. Continuous flow synthesis of 6-monoamino-6-monodeoxy-β-cyclodextrin. Beilstein journal of organic chemistry 2023, 19, 294–302. doi:10.3762/bjoc.19.25
  • Jicsinszky, L.; Rossi, F.; Solarino, R.; Cravotto, G. Comparison of the Conventional and Mechanochemical Syntheses of Cyclodextrin Derivatives. Molecules (Basel, Switzerland) 2023, 28, 467. doi:10.3390/molecules28020467
  • Asif, M.; Imran, M. A chapter on synthesis of various heterocyclic compounds by environmentally friendly green chemistry technologies. Handbook of Greener Synthesis of Nanomaterials and Compounds; Elsevier, 2021; pp 69–108. doi:10.1016/b978-0-12-822446-5.00004-6
  • Molnár, Á. Synthetic Application of Cyclodextrins in Combination with Metal Ions, Complexes, and Metal Particles. ChemCatChem 2020, 13, 1424–1474. doi:10.1002/cctc.202001610
  • Menuel, S.; Saitzek, S.; Monflier, E.; Hapiot, F. Particle size effect in the mechanically assisted synthesis of β-cyclodextrin mesitylene sulfonate. Beilstein journal of organic chemistry 2020, 16, 2598–2606. doi:10.3762/bjoc.16.211
  • Schneider, R.; Sehlinger, A.; Meier, M. A. R. A Direct One-Pot Modification of β-Cyclodextrin via the Ugi-Five-Component Reaction. ChemistrySelect 2020, 5, 10765–10770. doi:10.1002/slct.202002367
  • Pedrazzo, A. R.; Caldera, F.; Zanetti, M.; Appleton, S. L.; Dhakar, N. K.; Trotta, F. Mechanochemical green synthesis of hyper-crosslinked cyclodextrin polymers. Beilstein journal of organic chemistry 2020, 16, 1554–1563. doi:10.3762/bjoc.16.127
  • Oliva, E.; Mathiron, D.; Rigaud, S.; Monflier, E.; Sevin, E.; Bricout, H.; Tilloy, S.; Gosselet, F.; Fenart, L.; Bonnet, V.; Pilard, S.; Djedaïni-Pilard, F. New Lipidyl-Cyclodextrins Obtained by Ring Opening of Methyl Oleate Epoxide Using Ball Milling. Biomolecules 2020, 10, 339. doi:10.3390/biom10020339
  • Jicsinszky, L.; Calsolaro, F.; Martina, K.; Bucciol, F.; Manzoli, M.; Cravotto, G. Reaction of oxiranes with cyclodextrins under high-energy ball-milling conditions. Beilstein journal of organic chemistry 2019, 15, 1448–1459. doi:10.3762/bjoc.15.145
  • Zhang, W.; Guo, T.; Wang, C.; He, Y.; Zhang, X.; Li, G.; Yizhi, C.; Jun, L.; Yangjing, L.; Xu, X.; Wu, L.; Zhang, S.; Zhang, J. MOF Capacitates Cyclodextrin to Mega-Load Mode for High-Efficient Delivery of Valsartan. Pharmaceutical research 2019, 36, 117. doi:10.1007/s11095-019-2650-3
  • Khan, R. I.; Pitchumani, K. Water-Soluble Palladium Complex of N′-(pyridin-2-yl)propane-1,3-diamine modified β-Cyclodextrin: An efficient Catalyst for Transfer Hydrogenation of Carbonyl Compounds. ACS Sustainable Chemistry & Engineering 2018, 6, 16130–16138. doi:10.1021/acssuschemeng.8b02787
  • Samanta, G. C.; Maiti, K.; Jayaraman, N. Glycosidic Bond Expanded Cyclic Oligosaccharides: Synthesis and Host-Guest Binding Property of a Cyclic Pentasaccharide. ACS omega 2018, 3, 7466–7473. doi:10.1021/acsomega.8b00580
  • Martín, J.; Díaz-Montaña, E. J.; Asuero, A. G. Cyclodextrins: Past and Present. Cyclodextrin - A Versatile Ingredient; InTech, 2018. doi:10.5772/intechopen.72736
  • Morin-Crini, N.; Winterton, P.; Fourmentin, S.; Wilson, L. D.; Fenyvesi, É.; Crini, G. Water-insoluble β-cyclodextrin–epichlorohydrin polymers for removal of pollutants from aqueous solutions by sorption processes using batch studies: A review of inclusion mechanisms. Progress in Polymer Science 2018, 78, 1–23. doi:10.1016/j.progpolymsci.2017.07.004
  • Peraro, C. R.; Anconi, A. C. S. A.; Anconi, C. P. A. Formation of β-Cyclodextrin inclusion compound with doxycycline: A theoretical approach. Chemical Physics Letters 2018, 692, 140–145. doi:10.1016/j.cplett.2017.12.024
  • Binello, A.; Cravotto, G.; Boffa, L.; Stevanato, L.; Bellumori, M.; Innocenti, M.; Mulinacci, N. Efficient and selective green extraction of polyphenols from lemon balm. Comptes Rendus. Chimie 2017, 20, 921–926. doi:10.1016/j.crci.2017.06.003
  • Anconi, C. P. A.; Santos, T. M. R.; Souza, A. C.; da Silva Borges, W. M.; Sales, A. L. R. Host–guest intermolecular hydrogen bonds and stability in aqueous media: the benzaldehyde/β-CD case study. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2017, 89, 137–142. doi:10.1007/s10847-017-0734-4
  • Jicsinszky, L.; Caporaso, M.; Martina, K.; Gaudino, E. C.; Cravotto, G. Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins. Beilstein journal of organic chemistry 2016, 12, 2364–2371. doi:10.3762/bjoc.12.230
  • Maiti, K.; Jayaraman, N. Synthesis and Structure of Cyclic Trisaccharide with Expanded Glycosidic Linkages. The Journal of organic chemistry 2016, 81, 4616–4622. doi:10.1021/acs.joc.6b00462

Patents

  • BAIER-GOSCHÜTZ ANGELA; FRIEBE ALEXANDER; NAPIERALA ROLAND; GÄBLER JULIANE. Hemocompatible adsorber for the dialysis of protein-bound uremic toxins. US 10625241 B2, April 21, 2020.
Other Beilstein-Institut Open Science Activities