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0003433022
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Vicens, J., Böhmer, V., Eds.; Kluwer: Dordrecht
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Calixarenes, a Versatile Class of Macrocyclic Compounds
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4
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0001670792
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Vögtle, F., Vol. Ed.; Pergamon Press: Oxford, UK
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(d) Pochini, A.; Ungaro, R. In Comprehensive Supramolecular Chemistry; Vögtle, F., Vol. Ed.; Pergamon Press: Oxford, UK, 1996; Vol. 2, p 103.
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Pochini, A.1
Ungaro, R.2
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Royal Society of Chemistry: Cambridge
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(e) Gutsche, C. D. Calixarenes Revisited; Royal Society of Chemistry: Cambridge, 1998.
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Gutsche, C.D.1
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6
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0004287470
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Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer Academic Publishers: Dordrecht
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(f) Calixarenes 2001; Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer Academic Publishers: Dordrecht, 2001.
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Calixarenes 2001
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Rappoport, Z., Ed., Wiley: Chichester; Chapter 19
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(g) Böhmer, V. In The Chemistry of Phenols; Rappoport, Z., Ed., Wiley: Chichester, 2003; Chapter 19.
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Böhmer, V.1
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9
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0001874297
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Görmar, G.; Seiffarth, K.; Schultz, M.; Zimmerman, J.; Flämig, G. Macromol. Chem. 1990, 191, 81.
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Görmar, G.1
Seiffarth, K.2
Schultz, M.3
Zimmerman, J.4
Flämig, G.5
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Seri, N.; Simaan, S.; Botoshansky, M.; Kaftory, M.; Biali, S. E. J. Org. Chem. 2003, 68, 7140.
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Seri, N.1
Simaan, S.2
Botoshansky, M.3
Kaftory, M.4
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Ito, K.; Izawa, S.; Ohba, T.; Ohba, Y.; Sone, T. Tetrahedron Lett. 1996, 37, 5959.
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Ito, K.1
Izawa, S.2
Ohba, T.3
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Sone, T.5
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12
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0010408737
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Compound 4 was first prepared by direct oxidation of 2. Ninagawa, A.; Cho, K.; Matsuda, H. Makromol. Chem. 1985, 186, 1379.
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Ninagawa, A.1
Cho, K.2
Matsuda, H.3
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13
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85044489326
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The four atropisomeric forms slowly equilibrate in DMSO-d6 at 150 °C. See: Akabori, S.; Sannohe, H.; Habata, Y.; Mukoyama, Y.; Ishii, T. J. J. Chem. Soc., Chem. Commun. 1996, 1467.
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Akabori, S.1
Sannohe, H.2
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Mukoyama, Y.4
Ishii, T.J.5
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14
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33751498991
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Jaime, C.; de Mendoza, J.; Prados, P.; Nieto, P. M.; Sanchez, C. J. Org. Chem. 1991, 56, 3372.
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Sanchez, C.5
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15
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0001980906
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Gutsche, C. D.; Dhawan, B.; Levine, J. A.; No, K. H.; Bauer, L. J. Tetrahedron 1983, 39, 403.
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Gutsche, C.D.1
Dhawan, B.2
Levine, J.A.3
No, K.H.4
Bauer, L.J.5
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16
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0001740088
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paco has been reported. See: Rizzoli, C.; Andreetti, G. D.; Ungaro, R.; Pochini, A. J. Mol. Struct. 1982, 82, 133.
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Rizzoli, C.1
Andreetti, G.D.2
Ungaro, R.3
Pochini, A.4
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17
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0003110217
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Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer Academic Publishers: Dordrecht
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For a review on the oxidation and reduction of calixarenes, see: Biali, S. E. In Calixarenes 2001; Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer Academic Publishers: Dordrecht, 2001; pp 266-279
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Calixarenes 2001
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Biali, S.E.1
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18
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3042811138
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note
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Although at present the rigidity of the calix[4]arene tetraacetate derivatives 5 and 6 is unknown, we assume, by analogy with 2, that in these compounds the bulky acetate groups preclude the rotation through the annulus of the rings, allowing the isolation of atropisomers at room temperature in the laboratory.
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19
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3042811404
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note
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1,2-alt.
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21
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3042770568
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note
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MM3(96) is included in the Sybyl 6.9 program package (Tripos Assoc., Inc., St. Louis, MO 63144).
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22
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0024821263
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(a) Allinger, N. L.; Yuh, Y. H.; Lii, J.-H. J. Am. Chem. Soc. 1989, 111, 8551.
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Allinger, N.L.1
Yuh, Y.H.2
Lii, J.-H.3
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25
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3042730027
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note
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-1). (Thondorf, I. Unpublished results.)
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