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Kluwer Academic Publishers
Reference66 articles.
1. For recent reviews on calixarenes see: a) V. Bühmer, Angew. Chem., Int. Ed. Engl. 1995, 34, 713–745. b) C. D. Gutsche, Aldrichimica Acta 1995, 28, 1–9 c) C. D. Gutsche, Calixarenes Revisited Royal Society of Chemistry, Cambridge, 1998.
2. G. Gürmar, K. Seiffarth, M. Schultz, J. Zimmermann, G. Flamig, Makromol. Chem. 1990, 191, 81–87. b) O. Aleksiuk and S. E. Biali, J. Org. Chem. 1996, 61, 5670–5673.
3. See for example: Z. Goren, S. E. Biali, J. Chem. Soc., Perkin Trans. 1 1990, 1484–1487. For a review on the hydroxyl replacement in calixarenes see: S. E. Biali, Isr. J. Chem. 1997, 37, 131–139.
4. a) Bicalix[n]arenes derivatives (n=4,6,8) connected by a biphenyl-like bond at the para-position of one ring are obtained by oxidation of calixarenes derivatives with FeCl3 6H2O in refluxing acetonitrile; b) P. Neri, A. Bottino, F. Cunsolo, M. Piatelli, E. Gavuzzo, Angew. Chem., Int. Ed. Engl. 1998, 37, 166–169; c) A. Bottino, F. Cunsolo, M. Piatelli, D. Garozzo, P. Neri, J. Org. Chem. 1999, 64, 8018–8020.
5. For reviews on the quinone group see: The chemistry of functional groups: The chemistry of quinonoid compounds, Part 1, S. Patai Ed, Wiley, Chichester (1974), Part 2, S. Patai, Z. Rappoport, Eds, Wiley, Chichester (1988).
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