Abstract
Salt bridges were used to attach polymerisable amidine monomers to an oligomeric benzoic acid template. CuAAC oligomerisation reactions in the presence of a benzoic acid 3-mer template gave the amidine 3-mer copy as the major product. Cleavage of ester linkers was used to hydrolyse off the amidine recognition units and convert the product into a benzoic acid 3-mer copy of the original template.
Cite
CITATION STYLE
APA
Núñez-Villanueva, D., & Hunter, C. A. (2022). Replication of a synthetic oligomer using chameleon base-pairs. Chemical Communications, 58(78), 11005–11008. https://doi.org/10.1039/d2cc04580j
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