797818-06-5Relevant academic research and scientific papers
Artificial receptors that provides a preorganized hydrophobic environment: A biomimetic approach to dopamine recognition in water
Kim, Jeongryul,Raman, Balamurali,Ahn, Kyo Han
, p. 38 - 45 (2007/10/03)
The recognition of dopamine in water has been achieved with tripodal oxazoline-based artificial receptors, capable of providing a preorganized hydrophobic environment by rational design, which mimics a hydrophobic pocket predicted for a human D2 receptor.
Molecular recognition of carbohydrates with acyclic pyridine-based receptors
Mazik, Monika,Radunz, Wolfgang,Boese, Roland
, p. 7448 - 7462 (2007/10/03)
The recognition capabilities of acyclic pyridine-based receptors toward monosaccharides were evaluated. Aminopyridine receptors based on the 2,4,6-trimethyl- or 2,4,6-triethylbenzene frame show high β vs α binding selectivity in the recognition of glucopyranosides. Amidopyridine receptors, which are sterically less hindered at nitrogen, display high efficiency and an inverse selectivity. The 2-aminopyridine group has been established as a highly effective recognition group in the binding of monosaccharides. The factors influencing the binding properties of receptors 1-15, which differ in the nature and number of binding and spacer subunits used as the buildings blocks, are discussed.
Novel arificial receptors for alkylammonium ions with remarkable selectivity and affinity
Kim, Sung-Gon,Ahn, Kyo Han
, p. 3399 - 3403 (2007/10/03)
The benzene-based tripodal tris(oxazolines) have been developed as the most selective and strong receptors toward linear alkylammonium ions reported to date. Among six tris(oxazolines) based on 2,4,6-trimethylbenzene framework, the phenylglycinol-derived
