Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Envirocat EPZ10: A Recyclable Solid Acid Catalyst for the Synthesis of Biginelli-type 3,4-Dihydropyrimidin-2(1H)-ones

  • Published : 2004.12.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Kappe, C. O. Eur. J. Med. Chem. 2000, 35, 1043. https://doi.org/10.1016/S0223-5234(00)01189-2
  2. Biginelli, P. Gazz. Chim. Ital. 1893, 23, 360.
  3. Folkers, K.; Harwood, H. J.; Johnson, T. B. J. Am. Chem. Soc.1932, 54, 3751. https://doi.org/10.1021/ja01348a040
  4. Yadav, J. S.; Reddy, B. V. S.; Srinivas, R.; Venugopal, C.;Ramalingam, T. Synthesis 2001, 1341.
  5. Ma, Y.; Qian, C.;Wang, L.; Yang, M. J. Org. Chem. 2000, 65, 3864. https://doi.org/10.1021/jo9919052
  6. Gohain, M.;Prajapati, D.; Sandhu, J. S. Synlett 2004, 235.
  7. Kumar, K. A.; Kasthuraiah, M.; Reddy, C. S.; Reddy, C. D. Tetrahedron Lett.2001, 42, 7873. https://doi.org/10.1016/S0040-4039(01)01603-3
  8. Varala, R.; Alam, M. M.; Adapa, S. R. Synlett2003, 67.
  9. Bose, D. S.; Fatima, L.; Mereyala, H. B. J. Org.Chem. 2003, 68, 587. https://doi.org/10.1021/jo0205199
  10. Paraskar, A. S.; Dewkar, G. K.; Sudalai,A. Tetrahedron Lett. 2003, 44, 3305. https://doi.org/10.1016/S0040-4039(03)00619-1
  11. Lu, J.; Bai, Y. Synthesis2002, 466.
  12. Hu, E. H.; Sidler, D. R.; Dolling, Ulf-H. J. Org.Chem. 1998, 63, 3454. https://doi.org/10.1021/jo970846u
  13. Reddy, C. V.; Mahesh, M.; Raju, P. V.K.; Babu, T. R.; Reddy, V. V. N. Tetrahedron Lett. 2002, 43, 2657. https://doi.org/10.1016/S0040-4039(02)00280-0
  14. Dondoni, A.; Massi, A. Tetrahedron Lett. 2001, 42, 7975. https://doi.org/10.1016/S0040-4039(01)01728-2
  15. Jin, T.; Zhang, S.; Li, T. Synth. Commun. 2002, 32, 1847. https://doi.org/10.1081/SCC-120004068
  16. Salehi, P.; Dabiri, M.; Zolfigol, M. A.; Fard, M. A. B. TetrahedronLett. 2003, 44, 2889. https://doi.org/10.1016/S0040-4039(03)00436-2
  17. Tu, S.; Fang, F.; Zhu, S.; Li, T.; Zhang,X.; Zhuang, Q. Synlett 2004, 537.
  18. Bigi, F.; Carloni, S.;Frullanti, B.; Maggi, R.; Sartori, G. Tetrahedron Lett. 1999, 40,3465. https://doi.org/10.1016/S0040-4039(99)00424-4
  19. Anastas, P. T.; Warner, J. C. Green Chemistry: Theory andPractice; Oxford University, 1998.
  20. Barlow, S. J.; Bastock, T. W.; Clark, J. H.; Cullen, S. R.Tetrahedron Lett. 1993, 34, 3339. https://doi.org/10.1016/S0040-4039(00)73698-7
  21. Kappe, C. O. J. Org. Chem. 1997, 62, 7201. https://doi.org/10.1021/jo971010u

Cited by

  1. Immobilized on Activated Charcoal vol.187, pp.4, 2012, https://doi.org/10.1080/10426507.2011.631644
  2. )-Ones Using Recyclable Amberlyst 15 DRY as a Heterogeneous Catalyst via Three-Component Biginelli-Like Reaction vol.2012, pp.2090-5157, 2012, https://doi.org/10.5402/2012/480989
  3. Novel and Chemoselective Dehydrogenation of 3,4-Dihydropyrimidin-2(1H)-ones with 1,4-Bis(triphenylphosphonium)-2-butene Peroxodisulfate vol.34, pp.6, 2013, https://doi.org/10.5012/bkcs.2013.34.6.1751
  4. The Combined Role of Catalysis and Solvent Effects on the Biginelli Reaction: Improving Efficiency and Sustainability vol.19, pp.16, 2013, https://doi.org/10.1002/chem.201204396
  5. Carbonyl–olefin metathesis: a key review vol.5, pp.8, 2018, https://doi.org/10.1039/C7QO01037K
  6. Envirocat EPZ10: A Recyclable Solid Acid Catalyst for the Synthesis of Biginelli-Type 3,4-Dihydropyrimidin-2(1H)-ones. vol.36, pp.22, 2005, https://doi.org/10.1002/chin.200522160
  7. Synthesis, characterization and applications of coordination polymers of Ln(III) pp.10990739, 2008, https://doi.org/10.1002/aoc.1460
  8. 2D Oxide Nanomaterials to Address the Energy Transition and Catalysis vol.31, pp.3, 2018, https://doi.org/10.1002/adma.201801712
  9. Microwave-induced protection and deprotection of 4-oxo-(4H)-1-benzopyran-3-carbaldehydes catalysed by Envirocat EPZ10R vol.17, pp.1, 2004, https://doi.org/10.1016/j.mencom.2007.01.017
  10. Catalysis by layered materials: A review vol.107, pp.1, 2004, https://doi.org/10.1016/j.micromeso.2007.03.011
  11. One-Pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones and Their Sulfur Derivatives with H2SO4Supported on Silica Gel or Alumina vol.184, pp.7, 2004, https://doi.org/10.1080/10426500802293153
  12. NaHSO4·H2O as a Heterogeneous Acidic Reagent for Mild and Convenient Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones and Their Sulfur Derivatives vol.184, pp.9, 2004, https://doi.org/10.1080/10426500802501274
  13. A chemical placebo: NaCl as an effective, cheapest, non-acidic and greener catalyst for Biginelli-type 3,4-dihydropyrimidin-2(1H)-ones (-thiones) synthesis vol.13, pp.1, 2004, https://doi.org/10.1007/s11030-008-9094-8
  14. Al(HSO4)3/silica gel as a novel catalytic system for the ring opening of epoxides with thiocyanate anion under solvent-free conditions vol.21, pp.2, 2010, https://doi.org/10.1016/j.cclet.2009.10.030
  15. Nickel Nanoparticles: An Ecofriendly and Reusable Catalyst for the Synthesis of 3,4-Dihydropyrimidine-2(1H)-ones via Biginelli Reaction vol.31, pp.2, 2004, https://doi.org/10.5012/bkcs.2010.31.02.351
  16. A piperidinium triflate catalyzed Biginelli reaction vol.66, pp.16, 2004, https://doi.org/10.1016/j.tet.2010.02.067
  17. Grindstone chemistry: a highly efficient and green method for synthesis of 3,4-dihydropyrimidin-2-(1H)-ones byL-tyrosine as an organocatalyst: a combined experimental and DFT study vol.4, pp.67, 2004, https://doi.org/10.1039/c4ra05244g
  18. Biginelli Reaction: Polymer Supported Catalytic Approaches vol.21, pp.3, 2019, https://doi.org/10.1021/acscombsci.8b00120
  19. A nanocrystalline CdS thin film as a heterogeneous, recyclable catalyst for effective synthesis of dihydropyrimidinones and a new class of carbazolyl dihydropyrimidinones via an improved Biginelli pro vol.43, pp.27, 2019, https://doi.org/10.1039/c9nj02139f
  20. Envirocat EPZ-10: An Efficient Catalyst for the Synthesis of 1,2,4- Triazolidine-3-thiones vol.17, pp.4, 2004, https://doi.org/10.2174/1570178616666191019144317