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The Synthesis of p-Nitrocalix[4]arene

  • Published : 1986.08.20

Abstract

Methods for the preparation of p-nitrocalix[4]-arene via the direct substitution reaction of the p-tert-butylcalix[4]arene which is readily available with high yield from the base-induced direct condensation reaction procedure are described.

Keywords

References

  1. Acc. Chem. Res. v.16 C.D. Gutsche
  2. Abstracts of the 11th Midwest Regional Meeting of the ACS no.517 C.D. Gutsche;T.C. Kung;M.L. Hsu
  3. J. Am. Chem. Soc. v.103 C.D. Gutsche;B. Dhawan;K.H. No;R. Muthukrishnan
  4. Makromol. Chem. Rapid Commun. v.3 A. Ninagawa;H. Matsuda
  5. Makromol. Chem. Rapid Commun. v.3 Y. Nakamoto;S. Ishida
  6. US patent 4,259,464 R. Buriks;A.R. Fauke;J.H. Munch
  7. J. Am. Chem. Soc. v.104 C.D. Gutsche;J.A. Levine
  8. Synthesis M. Tashiro
  9. Org. Prep. Proc. Int. v.10 D. Bohmer;H. Rathay;H. Kammerrer
  10. Tetrahedron Lett. v.26 S. Shinkai;T. Tsubaki;T. Sone;O. Manabe
  11. Ann. Chem. v.277 J.L. Bridge

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  1. ChemInform Abstract: The Synthesis of p‐Nitrocalix(4)arene. vol.18, pp.16, 1986, https://doi.org/10.1002/chin.198716182
  2. Proximally functionalized cavitands and synthesis of a flexible hemicarcerand vol.19, pp.1, 1986, https://doi.org/10.1007/bf00708981
  3. New Synthetic Method ofp-Nitrocalixarenes vol.27, pp.21, 1997, https://doi.org/10.1080/00397919708007300
  4. Analytical Applications of Calixarenes vol.17, pp.2, 1986, https://doi.org/10.1515/revac.1998.17.2.69
  5. Synthesis and nitration of calix[4] (aza) crowns vol.18, pp.1, 2000, https://doi.org/10.1002/cjoc.20000180118
  6. Selective ipso-Nitration of tert-Butylcalix[4]arene Tripropylether vol.5, pp.7, 2000, https://doi.org/10.3390/50700941
  7. A CONVENIENT ONE POT ONE STEP SYNTHESIS OF p-NITROCALIXARENES VIA IPSONITRATION vol.31, pp.5, 2001, https://doi.org/10.1081/scc-100103269
  8. Wide-rim and outer-face functionalizations of calix[4]arene vol.233, pp.None, 2002, https://doi.org/10.1016/s0010-8545(02)00199-6
  9. Synthesis, characterization, and electrochemical and electrical properties of a novel ball-type hexanuclear metallophthalo-cyanine, bridged by calix[4]arenes substituted with four hexyl-thiometallopht vol.11, pp.9, 2007, https://doi.org/10.1142/s1088424607000734
  10. Synthesis of Calixsalen : A Route to Azacalixarene Analogue vol.28, pp.2, 1986, https://doi.org/10.5012/bkcs.2007.28.2.315
  11. Symmetrically tetrasubstituted p-nitrocalix[4]arenes: Synthesis, spectra and crystal structures vol.871, pp.1, 1986, https://doi.org/10.1016/j.molstruc.2007.01.052
  12. High-performance Liquid Chromatography Study of the Nitration Course of Tetrabutoxycalix[4]arene at the Upper Rim: Determination of the Optimum Conditions for the Preparation of 5,11,17-Trinitro-25,26 vol.27, pp.10, 1986, https://doi.org/10.1002/cjoc.200990341
  13. Selective nitration of calix[4]arenes that easily gave inherently chiral calix[4]arenes vol.80, pp.3, 1986, https://doi.org/10.1007/s10847-014-0413-7