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Microwave-Assisted Organocatalytic Synthesis of Tetrahydroquinolines via Hydride Transfer and Cyclization

  • 투고 : 2011.02.25
  • 심사 : 2011.03.31
  • 발행 : 2011.05.20

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참고문헌

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피인용 문헌

  1. ChemInform Abstract: Microwave-Assisted Organocatalytic Synthesis of Tetrahydroquinolines via Hydride Transfer and Cyclization. vol.42, pp.43, 2011, https://doi.org/10.1002/chin.201143161
  2. Enantioselective Conjugate Addition of 4-Hydroxycoumarin to Enones Catalyzed by Binaphthyl-Modified Primary Amine Organocatalyst vol.33, pp.6, 2012, https://doi.org/10.5012/bkcs.2012.33.6.1825
  3. Organocatalytic Synthesis of Tetrahydroquinolines from α,β-Unsaturated Ketones via 1,5-Hydride Transfer/Cyclization vol.34, pp.11, 2013, https://doi.org/10.5012/bkcs.2013.34.11.3463
  4. Enantioselective Michael Addition of 2-Hydroxy-1,4-naphthoquinone to β,γ-Unsaturated α-Keto Esters Catalyzed by Binaphthyl-Modified Squaramide vol.34, pp.6, 2013, https://doi.org/10.5012/bkcs.2013.34.6.1619
  5. Organocatalytic Enantioselective Michael Addition of Silyl Malonate to α,β-Unsaturated Enones: One-pot Synthesis of Chiral δ-Keto Esters vol.34, pp.9, 2013, https://doi.org/10.5012/bkcs.2013.34.9.2569
  6. 1,5-Hydride Transfer/Cyclization Catalyzed by Chiral Primary Amine Catalysts vol.355, pp.16, 2013, https://doi.org/10.1002/adsc.201300398
  7. Enantioselective One-Pot Synthesis of Ring-Fused Tetrahydroquinolines via Aerobic Oxidation and 1,5-Hydride Transfer/Cyclization Sequences vol.16, pp.20, 2014, https://doi.org/10.1021/ol502575f
  8. Asymmetric Synthesis of Tetrahydroquinolines via Saegusa-type Oxidative Enamine Catalysis/1,5-Hydride Transfer/Cyclization Sequences vol.3, pp.4, 2014, https://doi.org/10.1002/ajoc.201400022
  9. Enantioselective organocatalytic oxidative enamine catalysis–1,5-hydride transfer–cyclization sequences: asymmetric synthesis of tetrahydroquinolines vol.50, pp.2, 2014, https://doi.org/10.1039/C3CC46710D
  10. )-H Bond Activation vol.16, pp.3, 2016, https://doi.org/10.1002/tcr.201600003
  11. Synthesis of Ring-Fused 1-Benzazepines via [1,5]-Hydride Shift/7-Endo Cyclization Sequences vol.19, pp.6, 2017, https://doi.org/10.1021/acs.orglett.7b00184
  12. Enantioselective Conjugate Addition of Pyrazolones to Nitroalkenes Catalyzed by Binaphthyl-modified Squaramide Organocatalyst vol.38, pp.10, 2017, https://doi.org/10.1002/bkcs.11241
  13. -Phenyl Tetrahydroisoquinoline with β-Keto Acids vol.38, pp.12, 2017, https://doi.org/10.1002/bkcs.11307
  14. Synthesis of Ring-fused Tetrahydroquinoline Derivatives via [1,5]-Hydride Transfer/Cyclization Sequences vol.38, pp.5, 2017, https://doi.org/10.1002/bkcs.11126
  15. Enantioselective Michael Addition of 3-Aryl-Substituted Oxindoles to Methyl Vinyl Ketone Catalyzed by a Binaphthyl-Modified Bifunctional Organocatalyst vol.17, pp.6, 2012, https://doi.org/10.3390/molecules17067523
  16. -Phenyl Tetrahydroisoquinoline with β-Keto Acids vol.39, pp.1, 2018, https://doi.org/10.1002/bkcs.11354
  17. )-Ones with Aryldiazo Sulfones vol.39, pp.8, 2018, https://doi.org/10.1002/bkcs.11530
  18. Organocatalytic Asymmetric Conjugate Addition of 3-Alkyl-Substituted Oxindoles to Vinyl Ketones vol.33, pp.10, 2011, https://doi.org/10.5012/bkcs.2012.33.10.3171
  19. Organocatalytic Asymmetric Michael Addition of 1,3-Cyclohexanedione to β,γ-Unsaturated α-Keto Esters vol.33, pp.11, 2011, https://doi.org/10.5012/bkcs.2012.33.11.3537
  20. Organocatalytic Oxidative Enamine Catalysis and 1,5-Hydride Transfer/Cyclization: Synthesis of Tetrahydroquinoline Derivatives vol.34, pp.12, 2011, https://doi.org/10.5012/bkcs.2013.34.12.3891
  21. Recent development of direct asymmetric functionalization of inert C-H bonds vol.4, pp.12, 2011, https://doi.org/10.1039/c3ra46996d
  22. Visible Light Photoredox-Catalyzed Arylative Ring Expansion of 1-(1-Arylvinyl)cyclobutanol Derivatives vol.18, pp.18, 2011, https://doi.org/10.1021/acs.orglett.6b02201
  23. Visible Light Photoredox‐Catalyzed Arylation of Quinoxalin‐2(1 H )‐ones with Aryldiazonium Salts vol.3, pp.21, 2011, https://doi.org/10.1002/slct.201801431
  24. Progress in the Chemistry of Tetrahydroquinolines vol.119, pp.8, 2011, https://doi.org/10.1021/acs.chemrev.8b00567