Abstract
Easy scalable and eco-friendly syntheses of resorcin[5]arene, pyrogallol[5]arene, (2-nitro)resorcin[5]arene, (2-carboxyl)resorcin[5]arene, and resorcin[7]arene are presented and a wide range of upper-rim modifications is demonstrated. The macrocycles open the door toward expanding the rich covalent and supramolecular chemistry of [4]arenes with analogues having unique 5-fold and 7-fold symmetry.
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CITATION STYLE
APA
Chwastek, M., & Szumna, A. (2020). Higher analogues of resorcinarenes and pyrogallolarenes: Bricks for supramolecular chemistry. Organic Letters, 22(17), 6838–6841. https://doi.org/10.1021/acs.orglett.0c02357
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