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Richman J.E., Atkins T.J. J. Am. Chem. Soc. 96:1974;2268; (b) Vriesema B.K., Buter J., Kellogg R.M. J. Org. Chem. 49:1984;110; (c) Guggisberg, A.; Drandarov, K.; Hesse, M. Helv. Chim. Acta 2000, 83, 3035; (d) Drandarov, K.; Guggisberg, A.; Hesse, M. Helv. Chim. Acta 2002, 85, 979.
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Richman J.E., Atkins T.J. J. Am. Chem. Soc. 96:1974;2268; (b) Vriesema B.K., Buter J., Kellogg R.M. J. Org. Chem. 49:1984;110 Guggisberg, A.; Drandarov, K.; Hesse, M. Helv. Chim. Acta 2000, 83, 3035; Drandarov, K.; Guggisberg, A.; Hesse, M. Helv. Chim. Acta 2002, 85, 979.
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9
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0034746870
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and references cited therein
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12
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33845281675
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Kimura E., Koike T., Uenishi K., Hediger M., Kuramoto M., Joko S., Arai Y., Kodama M., Iitaka Y. Inorg. Chem. 26:1987;2975.
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17
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0010668084
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. For an alternative synthetic approach to compound 13, see: McManis J.S., Ganem B. J. Org. Chem. 45:1980;2041.
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McManis, J.S.1
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18
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0010631904
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note
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2c
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20
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37049075814
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Raston C.L., Skelton B.W., Whitaker C.R., White A.H. J. Chem. Soc., Dalton Trans. 1988;987.
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Raston, C.L.1
Skelton, B.W.2
Whitaker, C.R.3
White, A.H.4
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22
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0010594772
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+ in MeOH.
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23
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0010595975
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note
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--form (strong anionite, Fluka), corresponding to 10-fold excess of exchange capacity, then filtered and evaporated.
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24
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0010595976
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+).
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26
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0010595977
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note
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The present method was successfully used in our laboratory also for the preparation of a group of compounds similar to the polyazamacrolactams shown here (Yurdakul, A. et al. in preparation).
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