DOI QR코드

DOI QR Code

Substituent Chemical Shifts of 2-Aryl Derivatives of Benzimidazole, Benzimidazolium Ion, and Benzimidazoline

  • Published : 2008.11.20

Abstract

Keywords

References

  1. Tanner, D. D.: Chen, J. J. J. Org. Chem. 1989, 54, 3842 https://doi.org/10.1021/jo00277a020
  2. Tanner, D. D.: Chen, J. J. J. Org. Chem. 1992, 57, 662 https://doi.org/10.1021/jo00028a048
  3. Zhu, X.-Q.; Zhang, M.-T.; Yu, A.; Wang, C.-H.; Cheng, J.-P. J. Am. Chem. Soc. 2008, 130, 2501 https://doi.org/10.1021/ja075523m
  4. Lee, I.-S. H.; Kil, H. J.; Ji, Y. R. J. Phys. Org. Chem. 2007, 20, 484 https://doi.org/10.1002/poc.1182
  5. Craig, J. C.; Ekwuribe, N. N.; Fu, C. C.; Walker, K. A. M. Synthesis 1981, 303
  6. Lee, I.-S. H.; Jeoung, E. H.; Lee, C. K. J. Hetereocycl. Chem. 1996, 33, 1711 https://doi.org/10.1002/jhet.5570330627
  7. Pretsch, E.; Clerc, T.; Seibl, J.; Simon, W. Tables of Spectral Data for Structure Determination of Organic Compounds, 2nd ed.; 1989; pp C120-C125
  8. Craik, D. J.; Brownlee, R. T. C. Prog. Phys. Org. Chem. 1983, 14, 1 https://doi.org/10.1002/9780470171936.ch1
  9. Schulman, E. M.; Christensen, K. A.; Grant, D. M.; Walling, C. J. Org. Chem. 1974, 39, 2686 https://doi.org/10.1021/jo00932a004
  10. Hamer, G. K.; Peat, I. R.; Reynolds, W. F. Can. J. Chem. 1973, 51, 897 https://doi.org/10.1139/v73-135
  11. Robinson, C. N.; Stablein, G. E.; Slater, C. D. Tetrahedron 1990, 46, 335 https://doi.org/10.1016/S0040-4020(01)85418-1
  12. Pavia, D. L.; Lampman, G. M.; Kriz, G. S. Introduction to Spectroscopy, 3rd ed.; Harcourt, Inc.: Orlando, FL, 2001; pp A29-A30
  13. Breitmaier, E.; Voelter, W. Carbon-13 NMR Spectroscopy, 3rd ed.; VCH: Weinheim, Germany, 1987; p 110
  14. Lee, I.-S. H.; Jeoung, E. H.; Kreevoy, M. M. J. Am. Chem. Soc. 1997, 119, 2722 https://doi.org/10.1021/ja963768l
  15. Zhu, X.-Q.; Zhang, M.-T.; Yu, A.; Wang, C.- H.; Cheng, J.-P. J. Am. Chem. Soc. 2008, 130, 2501 https://doi.org/10.1021/ja075523m

Cited by

  1. How Much Does the Hybridization of a Carbon Atom Affect the Transmission of the Substituent Effect on the Chemical Shift? vol.36, pp.1, 2015, https://doi.org/10.1002/bkcs.10067
  2. Use of Correlation of 1H and 13C Chemical Shifts of N-Arylsuccinanilic Acids,N-Arylsuccinimides, N-Arylmaleanilic Acids, and N-Arylmaleimides with the Hammett Substituent Constan vol.30, pp.10, 2009, https://doi.org/10.5012/bkcs.2009.30.10.2351
  3. Hypoglycemic Function of Mulberry Leaf Polysaccharide and 1-Deoxynojirimycin (DNJ) vol.361, pp.None, 2008, https://doi.org/10.4028/www.scientific.net/amr.361-363.808
  4. Molecular structure and spectroscopic analysis of 1,4-Bis(1-methyl-2-benzimidazolyl)benzene; XRD, FT-IR, dispersive-Raman, NMR and DFT studies vol.103, pp.None, 2008, https://doi.org/10.1016/j.saa.2012.10.055
  5. Substituent effect study on the experimental 13C NMR chemical shifts of 3-(substituted phenyl)-3a,4,8,8a-tetrahydro-1,3-dioxepino[5,6-d] [1,2] isoxazoles vol.1193, pp.None, 2008, https://doi.org/10.1016/j.molstruc.2019.04.121
  6. Biosynthesis of MgO nanoparticles using Annona squamosa seeds and its catalytic activity and antibacterial screening vol.15, pp.1, 2008, https://doi.org/10.1049/mnl.2019.0358