DOI QR코드

DOI QR Code

Synthesis of Amlodipine Using Aza Diels-Alder Reaction

  • Published : 2002.01.20

Abstract

Keywords

References

  1. Triggle, D. J.; Lang, D. A.; Janis, R. A. Med. Res. Rev. 1989, 9, 123 https://doi.org/10.1002/med.2610090203
  2. Goldmann, S.; Stoltefuss, J. Angew. Chem. Int. Ed. Engl. 1991, 30, 1559 https://doi.org/10.1002/anie.199115591
  3. Hantzsch, A. Justus Liebigs Ann. Chem. 1882, 215, 1 https://doi.org/10.1002/jlac.18822150102
  4. Hinkel, L. E.; Ayling, E. E.; Morgan, W. H. J. Chem. Soc. 1931, 1835
  5. Campbell, S. F. US. Pat. 4,572,909. 1986
  6. Sircar, I.; Anderson, K. R. Tetrahedron Lett. 1988, 29, 6835 https://doi.org/10.1016/S0040-4039(00)88453-1
  7. De Koning, A. J.; Budzelaar, P. H. M.; Brandsma, L.; De Bie, M. J. A.; Boersma, J. Tetrahedron Lett. 1980, 21, 2105 https://doi.org/10.1016/S0040-4039(00)71499-7

Cited by

  1. Hantzsch Synthesis of 2,6-Dimethyl-3,5-dimethoxycarbonyl-4-(o-methoxyphenyl)-1,4-dihydropyridine; a Novel Cyclisation Leading to an Unusual Formation of 1-Amino-2-methoxycarbonyl-3,5-bis(o-methoxyphenyl)-4-oxa-cyclohexan-1-ene vol.12, pp.11, 2007, https://doi.org/10.3390/12112546
  2. ChemInform Abstract: Synthesis of Amlodipine Using Aza Diels-Alder Reaction. vol.33, pp.28, 2002, https://doi.org/10.1002/chin.200228172
  3. Structure elucidation of thermal degradation products of amlodipine vol.45, pp.8, 2007, https://doi.org/10.1002/mrc.2022
  4. An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles vol.9, pp.None, 2002, https://doi.org/10.3762/bjoc.9.265