| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275415 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
By reacting 3a-methylglycoluril and glycoluril with paraformaldehyde, monomethyl cucurbit[6]uril was synthesized in 14% yield. The new host molecule forms stable inclusion complexes with diamine and hexylaminocarbazole derivatives.
Graphical abstractBy reacting 3a-methylglycoluril and glycoluril with paraformaldehyde, monomethyl cucurbit[6]uril was synthesized in 14% yield. The new host molecule forms stable inclusion complexes with diamine and hexylaminocarbazole derivatives.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Synthesis and binding behaviors of monomethyl cucurbit[6]uril](/preview/png/5275415.png "First Page Preview: Synthesis and binding behaviors of monomethyl cucurbit[6]uril")
Authors
Mostafa M. Ahmed, Kazutaka Koga, Makoto Fukudome, Hideaki Sasaki, De-Qi Yuan,