References
- Dietrich, B. Pure Appl. Chem. 1993, 65, 1457. https://doi.org/10.1351/pac199365071457
- Atwood, J. L.; Holman, K. T.; Steed, J. W. Chem. Comm. 1996, 1401.
- Rason, L. Aust. J. Chem. 1976, 29, 1635. https://doi.org/10.1071/CH9761635
- Izatt, R. M.; Pawlak, K.; Bradshaw, J. S.; Bruening, R. L. Chem.Rev. 1991, 91, 1721. https://doi.org/10.1021/cr00008a003
- Beer, P. D.; Drew, M. G. B.; Hesek, D.; Nam, K. C. Chem. Comm. 1997, 107.
- Beer, P. D.; Drew, M. G. B.; Hodacova, J.; Stokes, S. E. J. Chem. Soc., Dalton Trans. 1995, 3447.
- Szemes, F.; Hesek, D.; Chem, Z.; Dent, S. W.; Drew, M. G. B.;Goulden, A. J.; Graydon, A. R.; Grieve, A.; Mortimer, R. J.; Wear,T.; Weightman, J. S.; Beer, P. D. Inorg. Chem. 1996, 35, 5868. https://doi.org/10.1021/ic960318l
- Beer, P. D.; Dent, S. W. Chem. Comm. 1998, 825.
- Fan, E.; Van Arman, S. A.; Kincaid, S.; Hamilton, A. D. J. Am.Chem. Soc. 1993, 115, 369. https://doi.org/10.1021/ja00054a066
- Scheerder, J.; Fochi, M.; Engbersen, J. F. L.; Reinhoudt, D. N. J.Org. Chem. 1994, 59, 7815. https://doi.org/10.1021/jo00104a044
- Scheerder, J.; Engbersen, J. F. L.; Casnati, A.; Ungaro, R.;Reinhoudt, D. N. J. Org. Chem. 1995, 60, 6448. https://doi.org/10.1021/jo00125a035
- Nam, K. C.; Kang, S. O.; Jeong, H. S.; Jeon, S. Tetrahedron Lett.1999, 40, 7343. https://doi.org/10.1016/S0040-4039(99)01505-1
- Jeong, H. S.; Choi, E. M.; Kang, S. O.; Nam, K. C.; Jeon, S. J.Electoanal. Chem. 2000, 485, 154. https://doi.org/10.1016/S0022-0728(00)00108-X
- Kang, S. O.; Oh, J. M.; Yang, Y. S.; Chun, J. C.; Jeon, S.; Nam, K.C. Bull. Korean Chem. Soc. 2002, 23, 145. https://doi.org/10.5012/bkcs.2002.23.1.145
- Gutsche, C. D.; See, K. A. J. Org. Chem. 1992, 57, 4527. https://doi.org/10.1021/jo00042a038
- Jaime, C.; Mendoza, J. D.; Parados, P.; Nieto, P. M.; Sanchez, C. J.Org. Chem. 1991, 56, 3372. https://doi.org/10.1021/jo00010a036
- Hynes, M. J. J. Chem. Soc. Dalton Trans. 1993, 311.
Cited by
- Calixarene-based Anion Receptors vol.17, pp.6, 2005, https://doi.org/10.1080/10610270500127089
- Synthesis and Anion Binding Properties of 2,5-Diamidothiophene Polypyrrole Schiff Base Macrocycles vol.7, pp.23, 2005, https://doi.org/10.1021/ol052162b
- Catalytic Approach for the Synthesis of bis‐Calixarenes vol.37, pp.4, 2007, https://doi.org/10.1080/00397910601055040
- Double Calixarenes and Their Analytical Applications vol.27, pp.1, 2008, https://doi.org/10.1515/REVAC.2008.27.1.1
- Conformational analysis and anion-binding properties of ferrocenyl-calixarene receptors vol.21, pp.1-2, 2009, https://doi.org/10.1080/10610270802527036
- Ion and Molecular Recognition by Lower Rim 1,3-Di-conjugates of Calix[4]arene as Receptors vol.111, pp.8, 2011, https://doi.org/10.1021/cr1004524
- A chiral polymer-based turn-on fluorescent sensor for specific recognition of hydrogen sulfate vol.50, pp.20, 2012, https://doi.org/10.1002/pola.26230
- Synthesis and Anion-Binding Properties of Novel Redox-Active Calixarene Receptors vol.2008, pp.25, 2008, https://doi.org/10.1002/ejoc.200800330
- Mass spectroscopic investigation of bis-1,3-urea calix[4]arenes and their ability to complex N-protected α-amino acids vol.66, pp.1-2, 2010, https://doi.org/10.1007/s10847-009-9687-6
- Synthesis and Anion Binding Properties of the Bridged Urea Derivatives of Calix[4]arene. vol.34, pp.40, 2003, https://doi.org/10.1002/chin.200340078
- Molecular Tweezer Based on Chenodeoxycholic Acid:Synthesis and Anion Binding Properties vol.25, pp.9, 2003, https://doi.org/10.5012/bkcs.2004.25.9.1411
- Novel anion receptors based on thiacalix[4]arene derivatives vol.60, pp.50, 2003, https://doi.org/10.1016/j.tet.2004.09.088
- Synthesis, X-ray Structure and Anion Binding Properties of the Novel Urea Derivatives of Calix[4]arene Dimer vol.26, pp.3, 2003, https://doi.org/10.5012/bkcs.2005.26.3.470
- A modular approach to organic, coordination complex and polymer based podand hosts for anions vol.250, pp.23, 2003, https://doi.org/10.1016/j.ccr.2006.06.004
- Microwave-Assisted Synthesis of Azocalixarenes vol.37, pp.13, 2003, https://doi.org/10.1080/00397910701397086