Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5264188 | Tetrahedron Letters | 2013 | 6 Pages |
Abstract
Neutral cyclic dimers of bile acid incorporating triazole and nonaromatic CH binding segments exhibit unique fluoride coordination properties and the formation of a 1:2 complex is confirmed. Remarkably, the aliphatic CH donors, which are activated and stabilized by the hyperconjugation as well as the electron-withdrawing effect of attached N-triazole and carbonyl groups, can present higher binding affinity than their triazole counterparts.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Weina Li, Qiong Xu, Yan Li, Wei Zhu, Jiecheng Cui, Yong Ju, Guangtao Li,