Document Type
Article
Publication Date
2-3-2022
Journal / Book Title
Chemical Communications
Abstract
Ring-opening of furans at the equatorial methylene bridge positions of a calix[4]arene gives access to a range of new molecules (in good yield) that have widespread potential impact in supramolecular chemistry amongst other areas.
DOI
10.1039/d1cc06889j
Montclair State University Digital Commons Citation
Fong, Angela; Campbell, Cameron L.; Huynh, Silvia; McCormick McPherson, Laura J.; Teat, Simon J.; Bebbington, Magnus W.P.; and Dalgarno, Scott J., "Facile synthetic routes to bridge-functionalised calix[4]arenes" (2022). Department of Chemistry and Biochemistry Faculty Scholarship and Creative Works. 624.
https://digitalcommons.montclair.edu/chem-biochem-facpubs/624
Rights
This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
Published Citation
Fong, A., Campbell, C. L., Huynh, S., McCormick McPherson, L. J., Teat, S. J., Bebbington, M. W. P., & Dalgarno, S. J. (2022). Facile synthetic routes to bridge-functionalised calix[4]arenes. Chemical communications (Cambridge, England), 58(20), 3302–3305. https://doi.org/10.1039/d1cc06889j