We report here the efficient synthesis of a series of [3]catenanes featuring the use of cucurbit[6]uril to simultaneously mediate the mechanical and covalent bond formations. By coupling the mechanical interlocking with covalent macrocyclization, formation of topological isomers is eliminated and the [3]catenanes are formed exclusively in good yields. The efficient access to these [3]cate-nanes and the presence of other recognition units render them promising building blocks for the construction of other high-order interlocked structures.
CITATION STYLE
Wing Hung Ng, A., Yee, C. C., Wang, K., & Au-Yeung, H. Y. (2018). Efficient catenane synthesis by cucurbit[6]uril-mediated azide–alkyne cycloaddition. Beilstein Journal of Organic Chemistry, 14, 1846–1853. https://doi.org/10.3762/bjoc.14.158
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