Bulletin of the Korean Chemical Society

  • 제29권8호
  • /
  • Pages.1594-1596
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  • 2008
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Highly Effective Total Synthesis of Benzofuran Natural Product Egonol

  • Choi, Da-Hye (Department of Chemistry and Institute of Natural Medicine, Hallym University) ;
  • Hwang, Jung-Woon (Department of Chemistry and Institute of Natural Medicine, Hallym University) ;
  • Lee, Hyun-Suck (Department of Chemistry and Institute of Natural Medicine, Hallym University) ;
  • Yang, Deok-Mo (Department of Chemistry and Institute of Natural Medicine, Hallym University) ;
  • Jun, Jong-Gab (Department of Chemistry and Institute of Natural Medicine, Hallym University)
  • 발행 : 2008.08.20
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참고문헌

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피인용 문헌

  1. Sonogashira Coupling Reaction pp.0022152X, 2013, https://doi.org/10.1002/jhet.770
  2. Benzofuran: an emerging scaffold for antimicrobial agents vol.5, pp.117, 2015, https://doi.org/10.1039/C5RA20658H
  3. 1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation vol.21, pp.2, 2016, https://doi.org/10.3390/molecules21020187
  4. Accessing a Biologically Relevant Benzofuran Skeleton by a One-Pot Tandem Heck Alkynylation/Cyclization Reaction Using Well-Defined Palladium N-Heterocyclic Carbene Complexes vol.55, pp.6, 2016, https://doi.org/10.1021/acs.inorgchem.5b02727
  5. Facile synthesis of naturally occurring nor-lignans (±)-Machicendiol and its analogs vol.47, pp.8, 2017, https://doi.org/10.1080/00397911.2017.1285936
  6. Total synthesis of natural products containing benzofuran rings vol.7, pp.39, 2017, https://doi.org/10.1039/C7RA03551A
  7. -Dihydronarciclasine vol.80, pp.6, 2017, https://doi.org/10.1021/acs.jnatprod.7b00208
  8. Synthesis, Evaluation for Cytotoxicity and Molecular Docking Studies of Benzo[c]furan-Chalcones for Potential to Inhibit Tubulin Polymerization and/or EGFR-Tyrosine Kinase Phosphorylation vol.19, pp.9, 2018, https://doi.org/10.3390/ijms19092552
  9. ChemInform Abstract: Highly Effective Total Synthesis of Benzofuran Natural Product Egonol. vol.40, pp.6, 2009, https://doi.org/10.1002/chin.200906212
  10. Facile Preparation of 2-Arylbenzo[b]furan Molecules and Their Anti-inflammatory Effects vol.31, pp.4, 2008, https://doi.org/10.5012/bkcs.2010.31.04.965
  11. Micro-Brillouin Spectroscopy Applied to the Glass Transition of Anti-inflammatory Egonol vol.14, pp.4, 2008, https://doi.org/10.3807/josk.2010.14.4.403
  12. Synthesis of egonol derivatives and their antimicrobial activities vol.19, pp.3, 2011, https://doi.org/10.1016/j.bmc.2010.12.044
  13. Rapid Access to Benzofuran‐Based Natural Products through a Concise Synthetic Strategy vol.2016, pp.12, 2008, https://doi.org/10.1002/ejoc.201600154
  14. One-Pot Tandem Hiyama Alkynylation/Cyclizations by Palladium(II) Acyclic Diaminocarbene (ADC) Complexes Yielding Biologically Relevant Benzofuran Scaffolds vol.3, pp.2, 2008, https://doi.org/10.1021/acsomega.7b01974