Efficient catenane synthesis by cucurbit[6]uril-mediated azide–alkyne cycloaddition

10Citations
Citations of this article
12Readers
Mendeley users who have this article in their library.

Abstract

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free