Orthocyclophanes. 7.¹ [1₄]Ketonand: Unexpected Formation and Its Rationalization by Calculation

References

1. Bull. Korean Chem. Soc. v.17 no.7 Orthocyclophanes. 6. Hexamethoxy Derivatives of [$1_6$]Orthocyclophane Lee, K. H.;Hong, J.-I.;Lee,W. Y.
2. J. Chem. Soc.,Perkin Trans. v.1 Lee, W. Y.;Sim, W.;Choi, K. D.
3. J. Chem. Soc., Perkin Trans. v.1 Lee, W. Y.;Sim, W.;Kim, H.-J.
4. J. Org. Chem. v.59 Lee, W. Y.;Park, C. H.;Kim, E. H.
5. Bull. Korean Chem. Soc. v.17 no.6 Lim, C. W.;Hong, J.-I.
6. Synthetic Multidentate Macrocyclic Compoonds Izatt, R. M.;Christensen, J. J.
7. The Chemistry of Ethers, Crown Ehters, Hudroxy Groups and Their Sulfur Analogues Patai, S.
8. Crown Compounds Hiroaka, M.
9. Progress in Macrocyclic Chemistry v.Ⅰ;Ⅱ Izatt, R. M.
10. Macrocyclic Polyether Synthesis Gokel, G. W.;Korzeniowski, S. H.
11. Crown Ethers and Analogs Weber, E.;Toner, J. L.;Goldberg, I.;Vogtle, F.;Laidler, D. A.;Stoddart, J. F.;Bartsch, R. A.;Liotta, G. L.
12. Cation Binding by Macrocycles Inoue, Y.;Gokel, G. W.
13. Chem. Rev. v.91 Izatt, R. M.;Pawlak, K.;Bradshaw. J. S.
14. Topics in Current Chemistry v.161 Weber, E.(Ed.)
15. J. Am. Chem. Soc. v.115 Lee, W. Y.;Park, C. H.;Kim, S.
16. J. Org. Chem. v.58 Lee, W. Y.;Park, C. H.
17. Synlett v.765 Lee, W. Y.
18. J. Org. Chem. v.59 Lee, W. Y.;Park, C. H.;Kim, H.-J.;Kim, S.
19. J. Org. Chem. v.57 Lee, W. Y.;Park, C. H.;Kim, Y. D.
20. J. Am. Chem. Soc. v.118 Cho, S. J.;Hwang, H. S.;Park, J. M.;Oh, K. S.;Kim. K. S.
21. J. Am. Chem. Soc. v.99 Dewar, M. J. S.;Thiel, W.
22. J. NRCC Software Catalog v.1 Dupuis, M.;Spangler, D.;Wendoloski, J.
23. J. Comput. Chem. v.7 Barker, J.
24. J. Phys. Chem. v.68 Bondi, A.
25. Protein Eng. v.2 van Gunsteren, W. F.
26. J. Comput. Chem. v.13 Wunz, T. P.
27. J. Am. Chem. Soc. v.117 Orozco, M.;Luque, F. J.
28. Discover User Guide(version 95.0.)