The syntheses of previously unknown sulfide- and telluride-pillar[]arenes are reported here. These macrocycles, among others, were tested as catalysts for alkylation reactions in aqueous solutions. Telluride-pillar[5]arene () showed the best performance, emulating the behavior of the methyltransferase enzyme cofactor -adenosyl-l-methionine. Using 1.0 mol % of , benzyl bromides reacted with NaCN/NaN in water, yielding organic nitriles/azides. The catalyst was recycled and efficiently reused for up to six cycles. H NMR experiments indicate a possible interaction between the substrate and 's cavity.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11421007 | PMC |
http://dx.doi.org/10.1021/acs.joc.4c00997 | DOI Listing |
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