DOI QR코드

DOI QR Code

Facile Syntheses of L-α-Glycerophosphorylcholine

  • Park, Jong-Moon (Hanyang University, Department of Chemistry and Applied Chemistry) ;
  • De Castro, Kathlia A. (Hanyang University, Department of Chemistry and Applied Chemistry) ;
  • Ahn, Hyun-Seok (Hanyang University, Department of Bionanotechnology) ;
  • Rhee, Hak-June (Hanyang University, Department of Chemistry and Applied Chemistry)
  • Received : 2010.06.15
  • Accepted : 2010.07.16
  • Published : 2010.09.20

Abstract

Keywords

References

  1. Bartus, R. T.; Dean, R. L.; Beer, B.; Lippa, A. S. Science 1982, 217, 408. https://doi.org/10.1126/science.7046051
  2. Larson, E. B.; Kukull, W. A.; Katzman, R. A. Annu. Rev. Public Health 1992, 13, 431. https://doi.org/10.1146/annurev.pu.13.050192.002243
  3. Geldmacher, D. S. Semin. Neurol. 2002, 22, 63. https://doi.org/10.1055/s-2002-33049
  4. Parnetti, L.; Amenta, F.; Gallai, V. Mech. Ageing Dev. 2001, 122, 2041. https://doi.org/10.1016/S0047-6374(01)00312-8
  5. De Jesus, M. Clin. Ther. 2003, 25, 178. https://doi.org/10.1016/S0149-2918(03)90023-3
  6. Tomassoni, D.; Avola, R.; Mignini, F.; Parnetti, L.; Amenta, F. Brain Res. 2006, 1120, 183. https://doi.org/10.1016/j.brainres.2006.08.068
  7. Hibino, H. Oreo Saiensu 2007, 7, 399.
  8. Schmidt, G.; Hershman, B.; Thannhauser, S. J. J. Biol. Chem. 1945, 161, 523.
  9. Baer, E.; Kates, M. J. Am. Chem. Soc. 1948, 70, 1394. https://doi.org/10.1021/ja01184a031
  10. Uziel, M.; Hanahan, D. J. J. Biol. Chem. 1956, 220, 1.
  11. Maurukas, J.; Holland, C. V. J. Org. Chem. 1961, 26, 608. https://doi.org/10.1021/jo01061a616
  12. Tronconi, G. EP 217765 A2, 1987.
  13. Puricelli, L. EP 486100 A1, 1992.
  14. Puricelli, L. EP 502357 A1, 1992.
  15. De Ferra, L.; Bonifacio, F.; Cifarelli, G.; Massardo, P.; Piccolo, O. EP 575717 A1, 1993.
  16. Kitaori, K.; Furukawa, Y.; Yoshimoto, H.; Otera, J. Tetrahedron 1999, 55, 14381. https://doi.org/10.1016/S0040-4020(99)00896-0
  17. Egri, G.; Balint, J.; Peredi, R.; Fogassy, E.; Novak, L.; Poppe, L. J. Mol. Catal. B 2000, 10, 583. https://doi.org/10.1016/S1381-1177(00)00141-7
  18. Iguchi, K.; Kitade, M.; Kashiwagi, T.; Yamada, Y. J. Org. Chem. 1993, 58, 5690. https://doi.org/10.1021/jo00073a030
  19. Guivisdalsky, P. N.; Bittman, R. J. Org. Chem. 1989, 54, 4643. https://doi.org/10.1021/jo00280a035
  20. Lindberg, J.; Ekeroth, J.; Konradsson, P. J. Org. Chem. 2002, 67, 194. https://doi.org/10.1021/jo010734+
  21. Andresen, T. L.; Jensen, S. S.; Madsen, R.; Jorgensen, K. J. Med. Chem. 2005, 48, 7305. https://doi.org/10.1021/jm049006f
  22. Rhee, H.; Park, J. M.; Lee, B. H. KR 2009039132 A, 2009.
  23. Milne, G. W. A. Drugs: Synonyms & Properties; Ashgate Pub. Co.: Brookfield, Vermont, USA, 2000; p 1280.
  24. Baer, E.; Kates, M. J. Am. Chem. Soc. 1948, 70, 1394. https://doi.org/10.1021/ja01184a031
  25. Tsujigami, T.; Sugai, T.; Ohta, H. Tetrahedron Asymm. 2001, 12, 2543. https://doi.org/10.1016/S0957-4166(01)00448-7
  26. Shaikh, T. M.; Sudalai, A. Tetrahedron Asymm. 2009, 20, 2287. https://doi.org/10.1016/j.tetasy.2009.08.027
  27. Puricelli, L. EP 0502357 A1, 1992.

Cited by

  1. ChemInform Abstract: Facile Syntheses of L-α-Glycerophosphorylcholine. vol.42, pp.8, 2011, https://doi.org/10.1002/chin.201108213
  2. H NMR study of the changes in brine- and dry-salted sea bass lipids under thermo-oxidative conditions: Both salting methods reduce oxidative stability vol.117, pp.4, 2015, https://doi.org/10.1002/ejlt.201400329
  3. Scalable Synthesis and Purification of Acetylated Phosphatidyl Choline Headgroup vol.21, pp.2, 2017, https://doi.org/10.1021/acs.oprd.6b00261
  4. in the aqueous phase pp.1029-2446, 2019, https://doi.org/10.1080/10242422.2019.1568413
  5. Enzymatic preparation of glycerophosphatilcholine catalyzed by combinational phospholipases: a comparative study of concertedversusstepwise catalysis vol.10, pp.64, 2020, https://doi.org/10.1039/d0ra07012b
  6. Two-stage Enzymatic Hydrolysis of Soybean Concentrated Phospholipid to Prepare Glycerylphosphorylcholine: Optimized by Response Surface Methodology vol.70, pp.2, 2010, https://doi.org/10.5650/jos.ess20261
  7. Chemical and Enzymatic Approaches to Esters of sn‐Glycero‐3‐Phosphoric Acid vol.2021, pp.29, 2010, https://doi.org/10.1002/ejoc.202100235
  8. Production of L-α-Glycerylphosphorylcholine from Oil Refining Waste Using a Novel Cold-Active Phospholipase B from Bacillus velezensis vol.9, pp.39, 2010, https://doi.org/10.1021/acssuschemeng.1c04767