References
- Gutsche, C. D. Calixarenes; Royal Society of Chemistry: Cambridge, 1989.
- Gutsche, C. D. In Synthesis of Macrocycles: Design of Selective Complexing Agents; Izatt, R. M.; Christensen, J. J., Eds.; Wiley: New York, 1987; p 93.
- Gutsche, C. D. Calixarenes Revisited; Royal Society of Chemistry: Cambridge, 1998.
- Bohmer, V.; McKervey, M. A. Chemie in Unserer Zeit 1991, 195.
- Gutsche, C. D. Calixarenes, Monographs in Supramolecular Chemistry; Stoddart, J. F., Ed.; Royal Society of Chemistry: Cambridge, U. K., 1989; Vol. 1.
- Gutsche, C. D. In Inclusion Compounds; Atwood, J. L.; Davies, J. E. D.; MacNicol, D. D., Eds.; Oxford University Press: New York, 1991; Vol. 4, pp27-63.
- Van Loon, J.-D.; Verboom, W.; Reinhoudt, D. N. Org. Prep. Proc. Int. 1992, 24, 437. https://doi.org/10.1080/00304949209356227
- Ungaro. R.; Pochini, A. In Frontiers in Supramolecular Organic Chemistry and Photochemistry; Schneider, H.-J., Eds.; VCH: Weinheim, Germany, 1991; pp 57-81.
- Calixarenes: A Versatile Class of Macrocyclic Compounds; Vicens, J.; Bohmer, V., Eds.; Kluwer: Dordrecht, 1991.
- Kumagai, H.; Hasegawa, M.; Miyanari, S.; Sugawa, Y.; Sato, Y.; Hori, T.; Ueda, S.; Kamiyama, H.; Miyano, S. Tetrahedron Lett. 1997, 38, 3972.
- Casnati, A.; Ungaro, R.; Asfari, Z.; Vicens, J. In Calixarenes 2001; Asfari, Z.; Böhmer, V.; Harrowfield, J.; Vicens, J., Eds; Kluwer Academic Publishers: Dordrecht, Holland, 2001; pp 365-384.
- Iki, N.; Morohashi, N.; Narumi, F.; Miyano, S. Bull. Chem. Soc. Jpn. 1998, 71, 1597. https://doi.org/10.1246/bcsj.71.1597
- Iki, N.; Kumakai, H.; Morohashi, N.; Ejima, K.; Hasegawa, M.; Miyanari, S.; Miyano, S. Tetrahedron Lett. 1998, 39, 7559. https://doi.org/10.1016/S0040-4039(98)01645-1
- Hosseini, W. In Calixarenes 2001; Asfari, Z.; Bohmer, V.; Harrowfield, J.; Vicens, J., Eds.; Kluwer Academic Publishers: Dordrecht, Holland, 2001.
- Lamare, V.; Dozol, J.-F.; Thuery, P.; Nierlich, M.; Asfari, Z.; Vicens, J. J. Chem. Soc. Perkin Trans. 2 2001, 1920.
- Grun, A.; Csokai, V.; Parlagh, G.; Bitter, I. Tetrahedron Lett. 2002, 43, 4153. https://doi.org/10.1016/S0040-4039(02)00764-5
- Lee, J. K.; Kim, S. K.; Sim, W.; Lee, S. W.; Vicens, J.; Miyano, S.; Kim, J. S. J. Org. Chem. 2003 (submitted).
- Katagiri, H.; Iki, N.; Hattori, T.; Kabuto, C.; Miyano, S. J. Am. Chem. Soc. 2001, 123, 779. https://doi.org/10.1021/ja005573q
- Lhotak, P. Tetrahedron 2001, 57, 4775. https://doi.org/10.1016/S0040-4020(01)00401-X
- Thuery, P.; Nierlich, M.; Bryan, J. C.; Lamare, V.; Dozol, J. F.; Asfari, Z.; Vicens, J. J. Chem. Soc., Dalton Trans. 1997, 4191.
- Thuery, P.; Nierlich, M.; Lamare, V.; Dozol, J. F.; Asfari, Z.; Vicens, J. J. Incl. Phen. Macro. Chem. 2000, 36, 375. https://doi.org/10.1023/A:1008079027142
- Nonius, BV Kappa-CCD Software; Delft: The Netherlands, 1998.
- Otwinowski, Z.; Minor, W. Methods Enzymol. 1997, 276, 307. https://doi.org/10.1016/S0076-6879(97)76066-X
- Sheldrick, G. M. SHELXS-97 and SHELXL-97; University of Gottingen, Germany, 1997.
- Spek, A. L. PLATON; University of Utrecht: The Netherlands, 2000.
- Sheldrick, G. M. SHELXTL, Version 5.1; Bruker AXS Inc.: Madison, WI, USA, 1999.
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