DOI QR코드

DOI QR Code

Nucleophilic Substitution Reactions of p-Nitrobenzyl Chloroformate


Abstract

Keywords

References

  1. The Chemistry of Acyl Halides Kivinen, A.;Patai, S.(ed.)
  2. Comprehensive of Acyl Halides v.10 Talbot, R. J. E.;Bam-ford, C. H.(ed.);Tipper, C. F. H.(ed.)
  3. J. Chem. Soc., Chem. Commun. Bentley, T. W.;Carter, G. E.;Harris, H. C.
  4. J. Chem. Soc., Perkin Trans. v.2 Bentley, T. W.;Carter, G. E.;Harris, H. C.
  5. J. Chem. Soc., Perkin Trans. v.2 Bentley, T. W.;Harris, H. C.
  6. J. Org. Chem. v.53 Bentley, T. W.;Harris, H. C.
  7. Bull. Korean Chem. Soc. v.3 Lee, I.;Koo, I. S.;Sohn, S. H.;Lee, H. H.
  8. J. Chem. Soc., Perkin Trans. v.2 Lee, I.;Sung, D. D.;Uhm, T. S.;Ryu, Z. H.
  9. J. Chem. Soc. Hudson, R. F.;Moss, G. E.
  10. J. Am. Chem. Soc. v.91 Kevill, D. N.;Foss, F. D.
  11. J. Chem. Soc., Perkin Trans. v.2 Kevill, D. N.;Knauss, D. C.
  12. Bull. Soc. Chim. Fr. v.383 Kevill, D. N.;Kim, C. B.
  13. J. Chem. Soc., Perkin Trans. v.2 Kevill, D. N.;Kim, C. B.
  14. J. Am. Chem. Soc. v.70 Grunwald, E.;Winstein, S.
  15. J. Am. Chem. Soc. v.73 Winstein, S.;Grunwald, E.;Jones, H. W.
  16. J. Org. Chem. v.56 Kevill, D. N.;Anderson, S. W.
  17. J. Am. Chem. Soc. v.104 Bentley, T. W.;Carter, G. E.
  18. Prog. Phys. Org. Chem. v.17 Bentley, T. W.;Llewellyn, G.
  19. J. Chem. Soc., Perkin Trans. v.2 Kevill, D. N.;D'Souza, M. J.
  20. J. Org. Chem. v.63 Kevill, D. N.;D'Souza, M. J.
  21. J. Org. Chem. v.55 Kevill, D. N.;Kyong, J. B.;Weitl, F. L.
  22. J. Chem. Res.(S) v.150 Kevill, D. N.;Kim, J. C.;Kyong, J. B.
  23. Bull. Korean Chem. Soc. v.21 Kyong, J. B.;Kim, Y. G.;Kim, D. K.;Kevill, D. N.
  24. J. Chem. Soc. B. Gold, V.;Grist, S.
  25. J. Phys. Org. Chem. v.6 Koo, I. S.;Lee, I.;Oh, J.;Yang, K.;Bentley, T. W.
  26. J. Chem. Soc., Perkin Trans. v.2 Yew, K. H.;Koh, H. J.;Lee, H. W.;Lee, I.
  27. J. Am. Chem. Soc. v.109 Song, B. D.;Jencks, W. P.
  28. Bull. Korean Chem. Soc. v.20 Koo, I. S.;Lee, S. I.;An, S. K.;Yang, K.;Lee, I.
  29. J. Chem. Soc., Perkin Trans. v.2 Carey, E.;More, O.;Vernon, N. M.
  30. J. Org. Chem. v.57 Kevill, D. N.;Kyong, J. B.
  31. Proc. Chem. Soc. Briody, J. M.;Satchell, D. P. N.
  32. J. Chem. Soc. Briody, J. M.;Satchell, D. P. N.
  33. J. Chem. Soc. Briody, J. M.;Satchell, D. P. N.
  34. J. Am. Chem. Soc. v.92 Ross, S. D.
  35. J. Org. Chem. USSR (English Trans.) v.12 Babaeva, L. G.;Bogatkov, S. V.;Grineva, N. A.;Kruglik-ova, R. I.
  36. J. Org. Chem. USSR (Engl. Transl.) v.19 Orlov, S. I.;Chimishkyan, A. L.;Grabarnik, M. S.
  37. J. Am. Chem. Soc. v.74 Carpenter, F. H.;Cish, D. T.

Cited by

  1. A Study of Solvolyses of ortho- and para Carboxybenzyl Bromides Using the Extended Grunwald-Winstein Equation vol.23, pp.11, 2002, https://doi.org/10.5012/bkcs.2002.23.11.1680
  2. Grunwald-Winstein Analysis - Isopropyl Chloroformate Solvolysis Revisited vol.10, pp.3, 2000, https://doi.org/10.3390/ijms10030862
  3. Analysis of the Nucleophilic Solvation Effects in Isopropyl Chlorothioformate Solvolysis vol.11, pp.7, 2000, https://doi.org/10.3390/ijms11072597
  4. Correlation of the Rates of Solvolysis of Neopentyl Chloroformate—A Recommended Protecting Agent vol.12, pp.2, 2000, https://doi.org/10.3390/ijms12021161
  5. Kinetic evaluation of the solvolysis of isobutyl chloro- and chlorothioformate esters vol.7, pp.None, 2000, https://doi.org/10.3762/bjoc.7.62
  6. A Study of Solvent Effects in the Solvolysis of Propargyl Chloroformate vol.2011, pp.None, 2011, https://doi.org/10.5402/2011/767141
  7. Detailed analysis for the solvolysis of isopropenyl chloroformate vol.2, pp.2, 2000, https://doi.org/10.5155/eurjchem.2.2.130-135.405
  8. Rate and Product Studies of 1-Adamantylmethyl Haloformates Under Solvolytic Conditions vol.33, pp.11, 2000, https://doi.org/10.5012/bkcs.2012.33.11.3657
  9. Statistical Methods for the Investigation of Solvolysis Mechanisms Illustrated by the Chlorides of the Carbomethoxy Protecting Groups NVOC and FMOC vol.2015, pp.None, 2000, https://doi.org/10.1155/2015/941638