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Schalley, C. A.; Castellano, R. K.; Brody, M. S.; Rudkevich, D. M.; Siuzdak, G.; Rebek, J. Jr. J. Am. Chem. Soc. 1999, 121, 4568.
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Schalley, C.A.1
Castellano, R.K.2
Brody, M.S.3
Rudkevich, D.M.4
Siuzdak, G.5
Rebek Jr., J.6
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0035887344
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Vysotsky, M. O.; Pop, A.; Broda, F.; Thondorf, I.; Böhmer, V. Chem. Eur. J. 2001, 7, 4403.
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Chem. Eur. J
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, pp. 4403
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Vysotsky, M.O.1
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Broda, F.3
Thondorf, I.4
Böhmer, V.5
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83
-
-
67651220446
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Frish, L.; Vysotsky, M. O.; Matthews, S. E.; Böhmer, V.; Cohen, Y. J. Chem. Soc., Perkin Trans. 2 2002, 83.
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J. Chem. Soc., Perkin Trans. 2
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Frish, L.1
Vysotsky, M.O.2
Matthews, S.E.3
Böhmer, V.4
Cohen, Y.5
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84
-
-
67651231929
-
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Frish, L.; Vysotsky, M. O.; Böhmer, V.; Cohen, Y. Org. Biomol. Chem. 2003, 9, 3375.
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Org. Biomol. Chem
, vol.9
, pp. 3375
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Frish, L.1
Vysotsky, M.O.2
Böhmer, V.3
Cohen, Y.4
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85
-
-
40849125470
-
-
Braekers, D.; Peters, C.; Bogdan, A.; Rudzevich, Y.; Böhmer, V.; Desreux, J. F. J. Org. Chem. 2008, 73, 701.
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J. Org. Chem
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Braekers, D.1
Peters, C.2
Bogdan, A.3
Rudzevich, Y.4
Böhmer, V.5
Desreux, J.F.6
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86
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54249147398
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-
Jiang, W.; Winkler, H. D. F.; Schalley, C. A. J. Am. Chem. Soc. 2008, 130, 13852.
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J. Am. Chem. Soc
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Jiang, W.1
Winkler, H.D.F.2
Schalley, C.A.3
-
87
-
-
67651220447
-
-
Regioisomeric dimers and enantiomers are not distinguished
-
Regioisomeric dimers and enantiomers are not distinguished.
-
-
-
-
88
-
-
67651203847
-
-
For the bis-loop derivative I, a similar compound with a bulky residue is possible, and for the mono-loop derivative G, two additional compounds with slim residues are possible. However, this would not enlarge the sorting possibilities.
-
For the bis-loop derivative I, a similar compound with a bulky residue is possible, and for the mono-loop derivative G, two additional compounds with slim residues are possible. However, this would not enlarge the sorting possibilities.
-
-
-
-
89
-
-
67651224553
-
-
From n objects, the first can form n different dimers, including its homodimer. The second one can form n, 1 dimers additionally, the dimer with the first object already being counted. The third one can form n, 2, and so on, and for the last one only its homodimer remains as a possibility. Thus, the number of dimers is given by: S, n, n, 1, n, 2, 2, 1. When the first and the last term are added, as well as the second and the penultimate, and so on, this can be rearranged to: S, n, 1, n, 1, 2, n, 2, 3, 0.5·n·n, 1
-
From n objects, the first can form n different dimers, including its homodimer. The second one can form n - 1 dimers additionally, the dimer with the first object already being counted. The third one can form n - 2, and so on, and for the last one only its homodimer remains as a possibility. Thus, the number of dimers is given by: S = n + (n - 1) + (n - 2) + ... + 2 + 1. When the first and the last term are added, as well as the second and the penultimate, and so on, this can be rearranged to: S = [n + 1] + [(n - 1) + 2] + [(n - 2) + 3] + ... = 0.5·n·(n + 1).
-
-
-
-
90
-
-
67651210097
-
-
It is not even necessary that all eleven tetraureas are present in the same quantity; only the pairs K/A, J/B, I/C, H/D, and G/E must be present in stoichiometric amounts.
-
It is not even necessary that all eleven tetraureas are present in the same quantity; only the pairs K/A, J/B, I/C, H/D, and G/E must be present in stoichiometric amounts.
-
-
-
-
91
-
-
67651206917
-
-
10O-chains connecting adjacent phenyl groups
-
10O-chains connecting adjacent phenyl groups
-
-
-
-
92
-
-
70349769687
-
-
Rudzevich Y., Rudzevich V., Klautsch F., Schalley C. A., Böhmer V. Angew. Chem. Int. Ed. 2009, 48, 3867;
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(2009)
Angew. Chem. Int. Ed
, vol.48
, pp. 3867
-
-
Rudzevich, Y.1
Rudzevich, V.2
Klautsch, F.3
Schalley, C.A.4
Böhmer, V.5
-
93
-
-
67651243327
-
-
Angew. Chem. 2009, 121, 3925.
-
(2009)
Angew. Chem
, vol.121
, pp. 3925
-
-
-
94
-
-
27844544309
-
-
For pentacalix[4]arenes obtained by the attachment of four tetraurea calix[4]arenes to the narrow rim of a fifth calix[4]arene in the 1,3-alternate conformation, see: Rudzevich, Y.; Fischer, K.; Schmidt, M.; Böhmer, V. Org. Biomol. Chem. 2005, 3, 3916.
-
For pentacalix[4]arenes obtained by the attachment of four tetraurea calix[4]arenes to the narrow rim of a fifth calix[4]arene in the 1,3-alternate conformation, see: Rudzevich, Y.; Fischer, K.; Schmidt, M.; Böhmer, V. Org. Biomol. Chem. 2005, 3, 3916.
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-
-
-
96
-
-
14844343123
-
-
(a) Rudzevich, Y.; Rudzevich, V.; Schollmeyer, D.; Thondorf, I.; Böhmer, V. Org. Lett. 2005, 7, 613.
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(2005)
Org. Lett
, vol.7
, pp. 613
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-
Rudzevich, Y.1
Rudzevich, V.2
Schollmeyer, D.3
Thondorf, I.4
Böhmer, V.5
-
97
-
-
22244434467
-
-
(b) Rudzevich, V.; Schollmeyer, D.; Braekers, D.; Desreux, J. F.; Diss, R.; Wipff, G.; Böhmer, V. J. Org. Chem. 2005, 70, 6027.
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(2005)
J. Org. Chem
, vol.70
, pp. 6027
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-
Rudzevich, V.1
Schollmeyer, D.2
Braekers, D.3
Desreux, J.F.4
Diss, R.5
Wipff, G.6
Böhmer, V.7
-
98
-
-
67651218356
-
-
In principle, the synthetic sequence allows also the introduction of two different alkyl ether residues Y if the respective ethers of the benzaldehyde 30 or phenol 31 are used.
-
In principle, the synthetic sequence allows also the introduction of two different alkyl ether residues Y if the respective ethers of the benzaldehyde 30 or phenol 31 are used.
-
-
-
-
99
-
-
33750209479
-
-
Rudzevich, Y.; Rudzevich, V.; Schollmeyer, D.; Thondorf, I.; Böhmer, V. Org. Biomol. Chem. 2006, 4, 3938.
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(2006)
Org. Biomol. Chem
, vol.4
, pp. 3938
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-
Rudzevich, Y.1
Rudzevich, V.2
Schollmeyer, D.3
Thondorf, I.4
Böhmer, V.5
-
100
-
-
2442626814
-
-
Shivanyuk, A.; Saadioui, M.; Broda, F.; Thondorf, I.; Vysotsky, M. O.; Rissanen, K.; Kolehmainen, E.; Böhmer, V. Chem. Eur. J. 2004, 10, 2138.
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(2004)
Chem. Eur. J
, vol.10
, pp. 2138
-
-
Shivanyuk, A.1
Saadioui, M.2
Broda, F.3
Thondorf, I.4
Vysotsky, M.O.5
Rissanen, K.6
Kolehmainen, E.7
Böhmer, V.8
-
101
-
-
67651215155
-
-
S symmetry.
-
S symmetry.
-
-
-
-
102
-
-
67651249176
-
-
From two regioisomeric dimers, only the distal arrangement is formed
-
From two regioisomeric dimers, only the distal arrangement is formed.
-
-
-
-
103
-
-
26844565176
-
-
Rudzevich, Y.; Rudzevich, V.; Moon, C.; Schnell, I.; Fischer, K.; Böhmer, V. J. Am. Chem. Soc. 2005, 127, 14168.
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(2005)
J. Am. Chem. Soc
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, pp. 14168
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Rudzevich, Y.1
Rudzevich, V.2
Moon, C.3
Schnell, I.4
Fischer, K.5
Böhmer, V.6
-
104
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-
85099487882
-
-
Rudzevich, Y.; Rudzevich, V.; Bolte, M.; Böhmer, V. Synthesis 2008, 754.
-
(2008)
Synthesis
, pp. 754
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Rudzevich, Y.1
Rudzevich, V.2
Bolte, M.3
Böhmer, V.4
-
105
-
-
45449112623
-
-
Rudzevich, Y.; Rudzevich, V.; Moon, C.; Brunklaus, G.; Böhmer, V. Org. Biomol. Chem. 2008, 6, 2270.
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(2008)
Org. Biomol. Chem
, vol.6
, pp. 2270
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-
Rudzevich, Y.1
Rudzevich, V.2
Moon, C.3
Brunklaus, G.4
Böhmer, V.5
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