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(b) S. L. Roberts, R. L. E. Furlan, S. Otto and J. K. M. Sanders, Org. Biomol. Chem., 2003, 1, 1625-1633;
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(d) A. L. Kieran, A. D. Bond, A. M. Belenguer and J. K. M. Sanders, Chem. Commun., 2003, 2674;
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Chem. Commun.
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(e) S. Otto, R. L. E. Furlan and J. K. M. Sanders, Science, 2002, 297, 590;
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Science
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(f) Y. Kubota, S. Sakamoto, K. Yamaguchi and M. Fujita, Proc. Natl. Acad. Sci. U. S. A., 2002, 99, 4854;
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Kubota, Y.1
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(h) E. Stulz, S. M. Scott, A. D. Bond, S. J. Teat and J. K. M. Sanders, Chem. Eur. J., 2003, 9, 6039-6048;
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Stulz, E.1
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9
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(i) M. M. Cai, X. D. Shi, V. Sidorov, D. Fabris, Y. F. Lam and J. T. Davis, Tetrahedron, 2002, 58, 661;
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10
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(j) G. R. L. Cousins, R. L. E. Furlan, Y.-F. Ng, J. E. Redman and J. K. M. Sanders, Angew. Chem. Int. Ed., 2001, 40, 423;
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Angew. Chem. Int. Ed.
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, pp. 423
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Cousins, G.R.L.1
Furlan, R.L.E.2
Ng, Y.-F.3
Redman, J.E.4
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(k) F. Hof, C. Nuckolls and J. Rebek, J. Am. Chem. Soc., 2000, 122, 4251;
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(l) M. Crego-Calama, P. Timmerman and D. N. Reinhoudt, Angew. Chem. Int. Ed., 2000, 39, 755;
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Crego-Calama, M.1
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For recent examples, see: (a) A. M. Whitney, S. Ladame and S. Balasubramanian, Angew. Chem. Int. Ed., 2004, 43, 1143;
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(b) R. Larsson, Z. Pei and O. Ramström, Angew. Chem. Int. Ed., 2004, 43, 3716;
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(c) H. Li, P. Williams, J. Micklefield, J. M. Gardiner and G. Stephens, Tetrahedron, 2004, 60, 753;
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Li, H.1
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(d) R. J. Lins, S. L. Flitsch, N. J. Turner, E. Irving and S. A. Brown, Tetrahedron, 2004, 60, 771;
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(e) M. Hochgürtel, H. Kroth, D. Piecha, M. W. Hofmann, C. Nicolaou, S. Krause, O. Schaaf, G. Sonnenmoser and A. V. Eliseev, Proc. Natl. Acad. Sci. U. S. A., 2002, 99, 3382;
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20
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B. Brisig, J. K. M. Sanders and S. Otto, Angew. Chem. Int. Ed., 2003, 42, 1270.
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Brisig, B.1
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4544263375
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(a) A. Bugaut, J.-J. Toulmé and B. Rayner, Angew. Chem. Int. Ed., 2004, 43, 3144;
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(b) N. Giuseppone, J.-L. Schmitt and J.-M. Lehn, Angew. Chem. Int. Ed., 2004, 43, 4902;
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(d) H. J. Cooper, M. A. Case, G. L. McLendon and A. G. Marshall, J. Am. Chem. Soc., 2003, 125, 5331;
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S. J. Rowan, S. J. Cantrill, G. R. L. Cousins, J. K. M. Sanders and J. F. Stoddart, Angew. Chem. Int. Ed., 2002, 41, 898-952.
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V. Goral, M. I. Nelen, A. V. Eliseev and J.-M. Lehn, Proc. Natl. Acad. Sci. U. S. A., 2001, 98, 1347.
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For examples of dynamic chemistry where the outcome is linkage-dependent, see: (a) O. Ramström, S. Lohman, T. Bunyapaiboonsri and J.-M. Lehn, Chem. Eur. J., 2004, 10, 1711;
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(b) K. C. Nicolaou, R. Hughes, S. Y. Cho, N. Winssinger, C. Smethurst, H. Labischinski and R. Endermann, Chem. Eur. J., 2001, 17, 3824;
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1 and 3 were obtained by S-acylation of 2 using a procedure adapted from: H. Y. Okuno, K. Uoto, T. T. Tomohiro and M.-T. Youinou, J. Chem, Soc., Dalton Trans., 1990, 3375. 2 was synthesized as reported in ref. 1e.
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2 was added at this stage to accelerate the oxidation process as described in: S. Capasso, C. A. Mattia, L. Mazzarella and R. Puliti, J. Chem. Soc., Perkin Trans. 2, 1980, 1297.
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0034699478
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Although all DCLs of macrocycles inevitably contain linear intermediates that, in principle, can be amplified (for an example, see: R. L. E. Furlan, G. R. L. Cousins and J. K. M. Sanders, Chem. Commun., 2000, 1761), the equilibrium concentration of linears will in general be so low, and their tendency to cyclise so high, that even very large template-induced amplifications will lead to modest yields.
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Chem. Commun.
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Furlan, R.L.E.1
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37
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18044397020
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note
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Parent monomers 1′ and 2′ are related to building blocks 1 and 2 respectively, as they carry the same individual functionalities.
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38
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0041863925
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Z. Grote, R. Scopelliti and K. Severin, Angew. Chem. Int. Ed., 2003, 42, 3821.
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