Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Benzoyl Rearrangement in Sythesis of Asymmetrically Substituted Calix[4]arenes

  • Kim, Jong-Min (Department of Chemistry, Chonnam National University) ;
  • Nam, Kye-Chun (Department of Chemistry, Chonnam National University)
  • Published : 1997.12.20
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References

  1. Calixarenes, Royal Society of Chemistry Gutsche, C. D.
  2. Calixarenes: A Versatile Class of Macrocyclic Compounds Vicens, J.;Bohmer, V.
  3. Angew. Chem. Int. Ed. Engl. v.34 Bohmer, V.
  4. Angew. Chem. Int. Ed. Engl. v.34 Zhang, L.;Godinez, L. A.;Lu, T.;Gokel, G. W.;Kaifer, A. E.
  5. J. Am. Chem. Soc. v.117 Casnati, A.;Pochini, A.;Ungaro, R.;Ugozzoli, F.;Arnaud, F;Fanni, S.;Sching, M.-J.;Egberink, R. J. M.;de Jong, F.;Reinhoudt, D. N.
  6. J. Am. Chem. Soc. v.111 Hofmeister, G. E.;Hahn, F. E.;Pedersen, S. F.
  7. Chem. Lett. Arimura, T.;Edamitsu, S.;Shinkai, S.;Manabe, O.;Muramatsu, T.;Tashiro, M.
  8. J. Org. Chem. v.59 Ferguson, G.;Gallagher, J. F.;Guinta, L.;Neri, P.;Pappalardo, S.;Parisi, M.
  9. Tetrahedron v.51 Verboom, W.;Bodewes, P. J.;van Essen, G.;Timmerman, P.;van Hummel, G. J.;Harkema, S.;Reinhoudt, D. N.
  10. J. Am. Chem. Soc. v.115 Iwamoto, K.;Shimizu, H.;Araki, K.;Shinkai, S.
  11. J. Inclusion Phenom. and Mol. Recognit. Chem. v.19 Bohmer, V.;Kraft, D.;Tabatabai, M.
  12. J. Org. Chem. v.60 Gonzalez, J. J.;Nieto, P. M.;Parados, P.;Echavarren, A. M.;de Mendoza, J.
  13. Chem. Commun. Markovsky, L. N.;Visotsky, M. A.;Pirozhenko, V. V.;Kalchenko, V. I.;Lipkowski, J.;Simonov, Y. A.
  14. Bull. Korean Chem. Soc. v.18 Kim, J. M.;Chun, J. C.;Nam, K. C.
  15. Bull. Korean Chem. Soc. v.17 Park, Y. J.;Shin, J. M.;Nam, K. C.;Kim, J. M.;Kook, S. K.
  16. J. Org. Chem. v.42 Pirkle, W. H.;Sikkenga, D. L.;Pavlin, M. S.
  17. J. Org. Chem. v.56 Jaime, C.;Mandoza, J. D.;Parados, P.;Nieto, P. M.;Sanchez, C.

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  6. Inherently Chiral Calixarenes: Synthesis and Applications vol.24, pp.8, 1997, https://doi.org/10.1002/chem.201703367