Bulletin of the Korean Chemical Society

  • 제23권5호
  • /
  • Pages.667-668
  • /
  • 2002
  • /
  • 0253-2964(pISSN)
  • /
  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
권호 표지
DOI QR코드

DOI QR Code

Microwave-assisted Kabachnik-Fields Reaction in Ionic Liquid

  • 발행 : 2002.05.20
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

키워드

참고문헌

  1. Welton, T. Chem. Rev. 1999, 99, 2071. https://doi.org/10.1021/cr980032t
  2. Wasserscheid, P.;Keim, W. Angew. Chem., Int. Ed. 2000, 39, 3772. https://doi.org/10.1002/1521-3773(20001103)39:21<3772::AID-ANIE3772>3.0.CO;2-5
  3. Brown, R.A.; Pollet, P.; McKoon, E.; Eckert, C. A.; Liotta, C. L.; Jessop, P.G. J. Am. Chem. Soc. 2001, 123, 1254. https://doi.org/10.1021/ja005718t
  4. Lee, S.-g.; Park, J. H.; Kang, J.; Lee, J. K. Chem. Commun.2001, 1698.
  5. Song, C. E.; Shim, W. H.; Roh, E. J.; Lee, S.-g.;Choi, J. H. Chem. Commun. 2001, 1122.
  6. Song, C. E.; Oh, C.R.; Roh, E. J.; Choo, D. J. Chem. Commun. 2000, 1743.
  7. Perreux,L.; Loupy, A. Tetrahedron 2001, 57, 9199. https://doi.org/10.1016/S0040-4020(01)00905-X
  8. Lidstrom, P.;Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225. https://doi.org/10.1016/S0040-4020(01)00906-1
  9. Dubreuil, J. F.; Bazureau, J. P. Tetrahedron Lett. 2000, 41,7351. https://doi.org/10.1016/S0040-4039(00)01237-5
  10. Dubreuil, J. F.; Bazureau, J. P. Tetrahedron Lett. 2001,42, 6097. https://doi.org/10.1016/S0040-4039(01)01190-X
  11. Varma, R. S.; Namboodiri, V. V. Pure Appl. Chem.2001, 73, 1309. https://doi.org/10.1351/pac200173081309
  12. Kabachnik, M. J.; Medved, T. Izv. Akad. Nauk SSSR 1954,1126.
  13. Firlds, E. K. J. Am. Chem. Soc. 1952, 74, 1528. https://doi.org/10.1021/ja01126a054
  14. Qian, C.; Huang, T. J. Org. Chem. 1998, 63, 4125. https://doi.org/10.1021/jo971242t
  15. Ranu, B.C.; Hajira, A.; Jana, U. Org. Lett. 1999, 1, 1141. https://doi.org/10.1021/ol990079g
  16. Manabe, K.;Kobayashi, S. Chem. Commun. 2000, 669.
  17. Kaboudin, B.; Nazari,R. Tetrahedron Lett. 2001, 42, 8211. https://doi.org/10.1016/S0040-4039(01)01627-6
  18. Chanderasekhar, S.;Prakash, S. J.; Jagadeshwar, V.; Narsihmulu, C. Tetrahedron Lett.2001, 42, 5561. https://doi.org/10.1016/S0040-4039(01)01053-X

피인용 문헌

  1. in Ionic Liquid by Microwave Irradiation vol.36, pp.17, 2006, https://doi.org/10.1080/00397910600781539
  2. ChemInform Abstract: Microwave-Assisted Kabachnik-Fields Reaction in Ionic Liquid. vol.33, pp.38, 2010, https://doi.org/10.1002/chin.200238169
  3. ] vol.11, pp.5, 2011, https://doi.org/10.1021/cg200064n
  4. The Kabachnik–Fields Reaction: Mechanism and Synthetic Use vol.17, pp.12, 2012, https://doi.org/10.3390/molecules171112821
  5. -Dodecylbenzenesulfonic Acid: A Highly Efficient Catalyst for One-Pot Synthesis of α-Aminophosphonates in Aqueous Media vol.24, pp.3, 2013, https://doi.org/10.1002/hc.21079
  6. -Bis(diphenylphosphinoylmethyl)glycine Esters by the Microwave-Assisted Double Kabachnik-Fields Reaction vol.24, pp.6, 2013, https://doi.org/10.1002/hc.21126
  7. A Critical Overview of the Kabachnik-Fields Reactions Utilizing Trialkyl Phosphites in Water as the Reaction Medium: A Study of the Benzaldehyde-Benzylamine Triethyl Phosphite/Diethyl Phosphite Models vol.25, pp.4, 2014, https://doi.org/10.1002/hc.21192
  8. Synthesis of α-aminophosphonates from α-hydroxyphosphonates; a theoretical study vol.27, pp.5, 2016, https://doi.org/10.1002/hc.21324
  9. [Et3NH][HSO4]-catalyzed one-pot, solvent-free synthesis and biological evaluation of α-amino phosphonates vol.42, pp.5, 2016, https://doi.org/10.1007/s11164-015-2348-z
  10. : A solid stable lewis acid catalyst for Michael addition of α-Aminophosphonates, Amines, Indoles and Pyrrole vol.193, pp.5, 2018, https://doi.org/10.1080/10426507.2017.1417298
  11. Microwave assisted synthesis and Anti-microbial activity of new Diethyl ((dialkoxyphosphoryl) (2-hydroxyphenyl) methyl) phosphoramidates vol.193, pp.5, 2018, https://doi.org/10.1080/10426507.2017.1418348
  12. Recent synthesis of aminophosphonic acids as potential biological importance vol.38, pp.1, 2010, https://doi.org/10.1007/s00726-009-0254-7
  13. Ytterbium(Ⅲ) Triflate-Catalyzed One-Pot Mannich-Type Reaction in Ionic Liquid vol.23, pp.10, 2002, https://doi.org/10.5012/bkcs.2002.23.10.1367
  14. InCl3-Catalyzed Regioselective Ring-Opening Reactions of Epoxides to β-Hydroxy Ethers vol.25, pp.6, 2002, https://doi.org/10.5012/bkcs.2004.25.6.881
  15. Microwave-assisted clean synthesis of 6-aryl-2,4-diamino-1,3,5-triazines in [bmim][PF6] vol.45, pp.27, 2004, https://doi.org/10.1016/j.tetlet.2004.04.195
  16. Aqueous [bmim][BF4] as Green Solvent in Microwave-assisted Organic Reactions: Clean Synthesis of 1H-benzo[f]chromene Derivatives vol.2006, pp.12, 2002, https://doi.org/10.3184/030823406780199767
  17. Amino-functionalized ionic liquid as catalytically active solvent for microwave-assisted synthesis of 4H-pyrans vol.8, pp.2, 2002, https://doi.org/10.1016/j.catcom.2006.05.031
  18. 1-Benzyl-3-Methyl Imidazolium Hydrogen Sulphate [bnmim][HSO4] Promoted Synthesis of α-Aminophosphonates vol.30, pp.5, 2002, https://doi.org/10.5012/bkcs.2009.30.5.1054
  19. Solvent-free sonochemical preparation of +/--aminophosphonates catalyzed by 1-hexanesulphonic acid sodium salt vol.17, pp.5, 2010, https://doi.org/10.1016/j.ultsonch.2010.02.002
  20. Microwave Assisted One-pot Synthesis of Novel α-Aminophosphonates and heir Biological Activity vol.31, pp.7, 2002, https://doi.org/10.5012/bkcs.2010.31.7.1863
  21. Silver‐Palladium Nanoalloys Modified Carbon Ionic Liquid Electrode with Enhanced Electrocatalytic Activity Towards Formaldehyde Oxidation vol.24, pp.10, 2012, https://doi.org/10.1002/elan.201200257
  22. SYNTHESIS AND BIOLOGICAL EVALUATIONS OF A SERIES OF NOVEL AZOLYL, AZINYL, PYRANYL, CHROMONYL AND AZEPINYL PHOSPHONATES vol.87, pp.12, 2013, https://doi.org/10.3987/com-13-12836
  23. A simple protocol for the synthesis ofα-substituted phosphonates vol.191, pp.9, 2016, https://doi.org/10.1080/10426507.2016.1167056
  24. K2CO3/Al2O3: An Efficient and Recyclable Catalyst for One-Pot, Three Components Synthesis of α-Aminophosphonates and Bioactivity Evaluation vol.31, pp.10, 2019, https://doi.org/10.14233/ajchem.2019.22194
  25. An Overview of Microwave‐Assisted Kabachnik‐Fields Reactions vol.5, pp.15, 2002, https://doi.org/10.1002/slct.202000693
  26. Stereochemistry of the Kabachnik‐Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite vol.5, pp.25, 2002, https://doi.org/10.1002/slct.202002369