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b) S. P. de Visser, S. Shaik, P. K. Sharma, D. Kumar, W. Thiel, J. Am. Chem. Soc. 2003, 125, 15779-15788;
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de Visser, S.P.1
Shaik, S.2
Sharma, P.K.3
Kumar, D.4
Thiel, W.5
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86
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a) V. Král, O. Rusin, F. P. Schmidtchen, Org. Lett. 2001, 3, 873-876;
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Král, V.1
Rusin, O.2
Schmidtchen, F.P.3
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b) R. D. Hubbard, S. R. Horner, B. L. Miller, J. Am. Chem. Soc. 2001, 123, 5810-5811;
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Hubbard, R.D.1
Horner, S.R.2
Miller, B.L.3
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C. S. Wilcox, N. M. Glagovich, Program HOSTEST5.6. University of Pittsburgh, Pittsburgh. PA, 1994.
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Wilcox, C.S.1
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a) C. Frassineti, S. Ghelli, P. Gans, A. Sabatini, M. S. Moruzzi, A. Vacca. Anal. Biochem. 1995, 251, 374-382;
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Frassineti, C.1
Ghelli, S.2
Gans, P.3
Sabatini, A.4
Moruzzi, M.S.5
Vacca, A.6
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23744500512
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K. J. Wallace, R. Hanes, E. Anslyn, J. Morey, K. V. Kilway, J. Siegel, J. Synthesis 2005, 2080-2083.
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J. Synthesis
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Wallace, K.J.1
Hanes, R.2
Anslyn, E.3
Morey, J.4
Kilway, K.V.5
Siegel, J.6
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93
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0003455624
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Pergamon, Amsterdam
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A. R. Katritzky, A. F. Pozharski, Handbook of Heterocyclic chemistry, Pergamon, Amsterdam, 2000, p. 131.
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Handbook of Heterocyclic chemistry
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Katritzky, A.R.1
Pozharski, A.F.2
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94
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53849105738
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1H NMR titrations were carried out; for each titration 15-20 samples were prepared.
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1H NMR titrations were carried out; for each titration 15-20 samples were prepared.
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95
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53849085772
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a was less than 10%;
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a was less than 10%;
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96
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53849120181
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12.
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12.
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97
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53849113277
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For each system, at least two fluorescence titrations were carried out: for each titration, 20 samples were prepared
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a) For each system, at least two fluorescence titrations were carried out: for each titration, 20 samples were prepared.
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98
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53849145286
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a estimation was less than 15%.
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a estimation was less than 15%.
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99
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0034682859
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For a discussion on limitations of the NMR method, see
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For a discussion on limitations of the NMR method, see: L. Fielding, Tetrahedron 2000, 56, 6151-6170.
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(2000)
Tetrahedron
, vol.56
, pp. 6151-6170
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Fielding, L.1
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100
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0002670428
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For an example of macrocyclic receptor that is able to distinguish between the octyl β-D-maltoside and octyl β-D-glucopyranoside in organic media CD3CN/CD3OD, 88:12 v/v, see; U, Neidlein, F. Diederich, Chem. Commun. 1996, 1493-1494
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3OD, 88:12 v/v). see; U, Neidlein, F. Diederich, Chem. Commun. 1996, 1493-1494.
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101
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53849144261
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For examples of CH⋯π interactions in the crystal structures of the complexes formed between artificial receptors and carbohydrates, see reference [3j
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For examples of CH⋯π interactions in the crystal structures of the complexes formed between artificial receptors and carbohydrates, see reference [3j].
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