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Mazik M, Kuschel M. (2008) Highly effective acyclic carbohydrate receptors consisting of aminopyridine, imidazole, and indole recognition units. Chemistry-A European Journal, 14, 2405-2419.
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6
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Molecular recognition of N-acetylneuraminic acid with acyclic benzimidazolium- and aminopyridine/guanidinium-based receptors
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Mazik M, Cavga H. (2007) Molecular recognition of N-acetylneuraminic acid with acyclic benzimidazolium- and aminopyridine/guanidinium-based receptors. European Journal of Organic Chemistry, 3633-3638.
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European Journal of Organic Chemistry
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Mazik, M.1
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7
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6344253005
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Molecular recognition of carbohydrates with acyclic pyridine-based receptors
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For other examples of carbohydrate receptors including 2-aminopyridine-based recognition groups, see: (a)
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For other examples of carbohydrate receptors including 2-aminopyridine-based recognition groups, see: (a) Mazik M, Radunz W, Boese R. (2004) Molecular recognition of carbohydrates with acyclic pyridine-based receptors. Journal of Organic Chemistry, 69, 7448-7462;
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Mazik, M.1
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8
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1642386040
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Pyridine-based receptors with high affinity for carbohydrates. Influence of the degree of steric hindrance at pyridine nitrogen on the binding mode
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(b) Mazik M, Sicking W. (2004) Pyridine-based receptors with high affinity for carbohydrates. Influence of the degree of steric hindrance at pyridine nitrogen on the binding mode. Tetrahedron Letters, 45, 3117-3121;
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Tetrahedron Letters
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9
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0442264163
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High □/□-anomer selectivity in molecular recognition of carbohydrates by artificial receptors
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(c) Mazik M, Radunz W, Sicking W. (2002) High □/□-anomer selectivity in molecular recognition of carbohydrates by artificial receptors. Organic Letters, 4, 4579-4582;
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Organic Letters
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Mazik, M.1
Radunz, W.2
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10
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0035793261
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Molecular recognition of carbohydrates by artificial receptors: Systematic studies towards recognition motifs for carbohydrates
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(d) Mazik M, Sicking W. (2001) Molecular recognition of carbohydrates by artificial receptors: Systematic studies towards recognition motifs for carbohydrates. Chemistry-A European Journal, 7, 664-670;
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Chemistry-A European Journal
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11
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Molecular recognition of carbohydrates by artificial polypyridine and polypyrimidine receptors
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(e) Mazik M, Bandmann H, Sicking W. (2000) Molecular recognition of carbohydrates by artificial polypyridine and polypyrimidine receptors. Angewandte Chemie, International Edition, 39, 551-554;
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12
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42349114342
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Amide, amino, hydroxy and aminopyridine groups as building blocks for carbohydrate receptors
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(f) Mazik M, Kuschel M. (2008) Amide, amino, hydroxy and aminopyridine groups as building blocks for carbohydrate receptors. European Journal of Organic Chemistry, 1517-1526;
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(2008)
European Journal of Organic Chemistry
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Mazik, M.1
Kuschel, M.2
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13
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33749141484
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Recognition properties of an acyclic biphenyl-based receptor toward carbohydrates
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(g) Mazik M, König A. (2006) Recognition properties of an acyclic biphenyl-based receptor toward carbohydrates. Journal of Organic Chemistry, 71, 7854-7857;
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(2006)
Journal of Organic Chemistry
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Mazik, M.1
König, A.2
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14
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33645774087
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Carboxylate-based receptors for the recognition of carbohydrates in organic and aqueous media
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(h) Mazik M, Cavga H. (2006) Carboxylate-based receptors for the recognition of carbohydrates in organic and aqueous media. Journal of Organic Chemistry, 71, 2957-2963;
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(2006)
Journal of Organic Chemistry
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15
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33644939001
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Crown ethers as building blocks for carbohydrate receptors
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DOI 10.1021/ol052902g
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(i) Mazik M, Kuschel M, Sicking W. (2006) Crown ethers as building blocks for carbohydrate receptors. Organic Letters, 8, 855-858. (Pubitemid 43411982)
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16
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0000970872
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Molecular recognition of cyclitols by neutral polyaza-hydrogen-bonding receptors: The strength and influence of intramolecular hydrogen bonds between vicinal alcohols
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For binding of cyclohexane diols and triols with compounds incorporating 2-aminopyridine units, see
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For binding of cyclohexane diols and triols with compounds incorporating 2-aminopyridine units, see: Huang CY, Cabell LA, Anslyn EV. (1994) Molecular recognition of cyclitols by neutral polyaza-hydrogen-bonding receptors: The strength and influence of intramolecular hydrogen bonds between vicinal alcohols. Journal of the American Chemical Society, 116, 2778-2792.
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For examples of CH-□ interactions in the crystal structures of the complexes formed between artificial receptors and carbohydrates, see
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For examples of CH-□ interactions in the crystal structures of the complexes formed between artificial receptors and carbohydrates, see: Mazik M, Cavga H, Jones PG. (2005) Molecular recognition of carbohydrates with artificial receptors: mimicking the binding motifs found in the crystal structures of protein-carbohydrate complexes. Journal of the American Chemical Society, 127, 9045-9052.
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Tuning and dissecting electronic and steric effects in ammonium receptors: Nonactin vs artificial receptors
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(a) Chin J, Oh J, Jon SY, Park SH, Walsdorff C, Stranix B, Ghoussoub A, Lee SJ, Chung HJ, Park SM, Kim K. (2002) Tuning and dissecting electronic and steric effects in ammonium receptors: nonactin vs artificial receptors. Journal of the American Chemical Society, 124, 5374-5379;
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(a) Mazik M, Buthe AC. (2007) Oxime-based receptors for mono- and disaccharide. Journal of Organic Chemistry, 72, 8319-8326;
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(b) Mazik M, Buthe AC. (2009) Recognition properties of receptors based on dimesitylmethane-derived core: Di- vs. monosaccharide preference. Organic & Biomolecular Chemistry, 7, 2063-2071;
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(c) Mazik M, Buthe AC. (2008) Highly effective receptors showing di- vs. monosaccharide preference. Organic & Biomolecular Chemistry, 6, 1558-1568. (Pubitemid 351555186)
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Determination of association constants (Ka) from solution NMR data
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Solvent effects in carbohydrate binding by synthetic receptors: Implications for the role of water in natural carbohydrate recognition
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For a discussion on solvent effects in carbohydrate binding by synthetic receptors, see: Klein E, Ferrand Y, Barwell NP, Davis AP. (2008) Solvent effects in carbohydrate binding by synthetic receptors: implications for the role of water in natural carbohydrate recognition. Angewandte Chemie, International Edition, 47, 2693-2696.
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Hydrogen and halogen bonding in the crystal structure of a 1,3,5-substituted 2,4,6-triethylbenzene consisting of three phenanthroline units
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44
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(a) Mazik M, Hartmann A, Jones PG. (2009) Highly effective recognition of carbohydrates by phenanthroline-based receptors: □- versus □-anomer binding preference. Chemistry-A European Journal, 15, 9147-9159;
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8-Hydroxyquinoline as a building block for artificial receptors: Binding preferences in the recognition of glycopyranosides
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(c) Mazik M, Geffert C. (2011) 8-Hydroxyquinoline as a building block for artificial receptors: binding preferences in the recognition of glycopyranosides. Organic & Biomolecular Chemistry, 9, 2319-2326;
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47
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Isopropylamino and isobutylamino groups as recognition sites for carbohydrates: Acyclic receptors with enhanced binding affinity toward β-galactosides
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(d) Mazik M, Sonnenberg C. (2010) Isopropylamino and isobutylamino groups as recognition sites for carbohydrates: Acyclic receptors with enhanced binding affinity toward β-galactosides. Journal of Organic Chemistry, 75, 6416-6423.
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For a discussion on selectivity in supramolecular host-guest complexes, see: Schneider H-J, Yatsimirsky A. (2008) Selectivity in supramolecular host-guest complexes. Chemical Society Reviews, 37, 263-277.
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