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For some rigid cycles with terpyridine units, see: G. R. Newkome, H.-W. Lee, J. Am. Chem. Soc. 1983, 105, 5956; J. L. Toner, Tetrahedron Lett. 1983, 24, 2707; T. W. Bell, A. Firestone, J. Am. Chem. Soc. 1986, 108, 8109; T. W. Bell, A. Firestone, R. Ludwig, J. Chem. Soc. Chem. Commun. 1989, 1902; T. W. Bell, P. J. Cragg, M. G. B. Drew, A. Firestone, D.-I. A. Kwok, Angew. Chem. 1992, 104, 319; Angew. Chem. Int. Ed. Engl. 1992, 31, 345; T. W. Bell, P. J. Cragg, M. G. B. Drew, A. Firestone, A. D.-I. Kwok, J. Liu, R. T. Ludwig, A. T. Papoulis, Pure Appl. Chem. 1993, 65, 361; U. Velten, M. Rehahn, Macromol. Chem. Phys. 1998, 199, 127. For some flexible cycles with terpyridine units, see: E. C. Constable, Prog. Inorg. Chem. 1994, 42, 67. For some other cycles with interior donor groups, see: Y. Tobe, N. Utsumi, A. Nagano, K. Naemura, Angew. Chem. 1998, 110, 1347; Angew. Chem. Int. Ed. 1998, 37, 1285; S. Höger, A.-D. Meckenstock, H. Pellen, J. Org. Chem. 1997, 62, 4556.
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The related 2,6-bis(tributylstannyl)pyridine has also been prepared by electrophilic stannylation from the corresponding dilithiopyridine. The yields, however, were lower: G. S. Hanan, U. S. Schubert, D. Volkmer, E. Rivière, J.-M. Lehn, N. Kyritsakas, J. Fischer, Can. J. Chem. 1997, 75, 169.
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(Ed.: E. W. Abel), Pergamon, Oxford
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This holds true for all other stannyls in this paper all well. For the toxicity of stannyl compounds, see: A. G. Davies, P. J. Smith, Comprehensive Organometalic Chemistry (Ed.: E. W. Abel), Pergamon, Oxford, 1982, 2, 608.
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53
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85033946566
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According to a CAS-online search as of July 20, 1998
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According to a CAS-online search as of July 20, 1998.
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