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Examples include: (a) Kimura, E. Crown Ethers and Analogous Compounds; Hiraoka, M., Ed.; Elsevier: Amsterdam, 1992; pp 381-478. (b) Edwards, M. L.; Snyder, R. D.; Stemerick, D. M. J. Med. Chem. 1991, 34, 2414-2420. (c) Scrimin, P.; Tecilla, P.; Tonellato, U.; Valle, G.; Veronese, A. J. Chem. Soc., Chem. Commun. 1995, 1163-1164.
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37049086355
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Examples include: (a) Kimura, E. Crown Ethers and Analogous Compounds; Hiraoka, M., Ed.; Elsevier: Amsterdam, 1992; pp 381-478. (b) Edwards, M. L.; Snyder, R. D.; Stemerick, D. M. J. Med. Chem. 1991, 34, 2414-2420. (c) Scrimin, P.; Tecilla, P.; Tonellato, U.; Valle, G.; Veronese, A. J. Chem. Soc., Chem. Commun. 1995, 1163-1164.
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(a) Edwards, M. L.; Snyder, R. D.; Stemerick, D. M. J. Med. Chem. 1991, 34, 2414-2420.
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Edwards, M.L.1
Snyder, R.D.2
Stemerick, D.M.3
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17
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0029032531
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and references therein
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(b) Mamos, P ; Karigiannis, G., Athanassopoulos, C.; Bichta, S.; Kalpaxis, D.; Papaioannou, D. Tetrahedron. Lett. 1995, 36, 5187-5190 and references therein.
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18
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0001592155
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(a) In polyazamacrocycle synthesis: Jazwinski, J.; Lehn, J.-M.; Méric, R.; Vigneron, J.-P.; Cesario, M.; Guilhem, J.; Pascard, C. Tetrahedron. Lett. 1987, 28, 3489-3492. (b) Overalkylation/deprotection in linear polyamine elaboration: Cetinkaya, E.; Hitchcock, P. B.; Jasim, H. A.; Lappert, M. F.; Spyropoulos, K. J. Chem. Soc., Perkin Trans. 1 1992, 561-567.
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Guilhem, J.6
Pascard, C.7
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19
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37049090489
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(a) In polyazamacrocycle synthesis: Jazwinski, J.; Lehn, J.-M.; Méric, R.; Vigneron, J.-P.; Cesario, M.; Guilhem, J.; Pascard, C. Tetrahedron. Lett. 1987, 28, 3489-3492. (b) Overalkylation/deprotection in linear polyamine elaboration: Cetinkaya, E.; Hitchcock, P. B.; Jasim, H. A.; Lappert, M. F.; Spyropoulos, K. J. Chem. Soc., Perkin Trans. 1 1992, 561-567.
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Lappert, M.F.4
Spyropoulos, K.5
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21
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0023262746
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(a) Wunz, T. P.; Dorr, R. T.; Alberts, D. S.; Tunget, C. L.; Einspahr, J.; Milton, S.; Remers, W. A. J. Med. Chem. 1987, 30, 1313.
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Wunz, T.P.1
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Milton, S.6
Remers, W.A.7
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23
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85033859429
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note
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1H NMR data for the crude intermediate material leading to 7 show a symmetrical species that corresponds to the expected imine structure.
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