Synthesis and complexation properties towards the ammonium cation of aza-coronand analogues containing sucrose.
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[1] Z. Ciunik,et al. Macrocyclic receptors containing sucrose skeleton , 2005 .
[2] S. Jarosz,et al. Regio- and Stereoselective Transformations of Sucrose at the Terminal Positions , 2002 .
[3] S. Jarosz,et al. Coupling of the C6 and C6′ Positions of Sucrose by Metathesis Reaction. , 2001 .
[4] S. Jarosz,et al. CROWN ETHER ANALOGS FROM SUCROSE , 2001 .
[5] L. Fielding. Determination of Association Constants (Ka) from Solution NMR Data , 2000 .
[6] J. Frelek,et al. Synthesis and Structural Analysis of Higher Analogs of Sucrose , 2000 .
[7] S. Immel,et al. Molecular modeling of saccharides, 7. The conformation of sucrose in water: A molecular dynamics approach† , 1995 .
[8] A. Stütz,et al. A simple convergent synthesis of the mannosidase inhibitor 1-deoxymannonojirimycin for sucrose , 1992 .
[9] F. Lichtenthaler. Carbohydrates as Organic Raw Materials , 2010 .
[10] A. Imberty,et al. Conformational behavior of sucrose and its deoxy analog in water as determined by NMR and molecular modeling , 1991 .
[11] D. Davies,et al. Co-operative and competitive hydrogen bonding in sucrose determined by SIMPLE 1H N.M.R. spectroscopy , 1985 .
[12] R. Lemieux,et al. The conformational properties of sucrose in aqueous solution: intramolecular hydrogen-bonding , 1982 .
[13] J. Lehn,et al. The [18]-N3O3 aza-oxa macrocycle: a selective receptor unit for primary ammonium cations , 1980 .