Thermodynamically Templated Macrocyclizations: Enhancing the Synthesis of Prism5arenes with Tailor-Made Guests

The macrocyclization of 2,6-dialkoxynaphthalene monomers to prism[5]arenes is thermodynamically templated by DABCO cations. In this study, we demonstrate that a greater template affinity for prism[5]arene improves the macrocyclization yield. By using novel templating cations, the yield of alkoxy-pri...

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Veröffentlicht in:Organic letters 2024-10, Vol.26 (39), p.8228
Hauptverfasser: Del Regno, Rocco, Palmieri, Anna, Della Sala, Paolo, Talotta, Carmen, De Rosa, Margherita, Campanile, Giuseppa, Argenio, Claudia, Gaeta, Carmine
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Sprache:eng
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Zusammenfassung:The macrocyclization of 2,6-dialkoxynaphthalene monomers to prism[5]arenes is thermodynamically templated by DABCO cations. In this study, we demonstrate that a greater template affinity for prism[5]arene improves the macrocyclization yield. By using novel templating cations, the yield of alkoxy-prism[5]arenes increases significantly compared with those of previously reported procedures, while the purification process becomes easier and faster.The macrocyclization of 2,6-dialkoxynaphthalene monomers to prism[5]arenes is thermodynamically templated by DABCO cations. In this study, we demonstrate that a greater template affinity for prism[5]arene improves the macrocyclization yield. By using novel templating cations, the yield of alkoxy-prism[5]arenes increases significantly compared with those of previously reported procedures, while the purification process becomes easier and faster.
ISSN:1523-7052
1523-7052
DOI:10.1021/acs.orglett.4c02590