Bulletin of the Korean Chemical Society

  • 제26권12호
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  • Pages.1925-1926
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  • 2005
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Tris-(pentafluorophenyl)phosphine Gold(I) Complexes as New Highly Efficient Catalysts for the Oxycarbonylation of Homopropargyl Carbonates

  • 발행 : 2005.12.20
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참고문헌

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피인용 문헌

  1. Gold(I)-Catalyzed Intramolecular Hydroamination of Alkyne with Trichloroacetimidates vol.8, pp.16, 2006, https://doi.org/10.1021/ol061307r
  2. Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity vol.115, pp.17, 2015, https://doi.org/10.1021/cr500691k
  3. Total Synthesis of Gelsemoxonine through a Spirocyclopropane Isoxazolidine Ring Contraction vol.137, pp.18, 2015, https://doi.org/10.1021/jacs.5b02574
  4. Influence in Fluorinated Gold(I) Coordination Compounds vol.2018, pp.40, 2018, https://doi.org/10.1002/ejic.201800567
  5. New Phosphine Ligand Architectures Lead to Efficient Gold Catalysts for Cycloisomerization Reactions at Very Low Loading pp.16154150, 2018, https://doi.org/10.1002/adsc.201800938
  6. Gold-Katalyse vol.118, pp.47, 2006, https://doi.org/10.1002/ange.200602454
  7. Gold Catalysis vol.45, pp.47, 2006, https://doi.org/10.1002/anie.200602454
  8. Gold-Katalyse: Isolierung von Vinylgold-Komplexen ausgehend von Alkinen vol.121, pp.44, 2009, https://doi.org/10.1002/ange.200903134
  9. Gold Catalysis: Isolation of Vinylgold Complexes Derived from Alkynes vol.48, pp.44, 2009, https://doi.org/10.1002/anie.200903134
  10. tris-(Pentafluorophenyl)phosphine Gold(I) Complexes as New Highly Efficient Catalysts for the Oxycarbonylation of Homopropargyl Carbonates. vol.37, pp.14, 2005, https://doi.org/10.1002/chin.200614156
  11. Molecular diversity through gold catalysis with alkynes vol.2007, pp.4, 2007, https://doi.org/10.1039/b612008c
  12. Cyclization of Propargylic Amides: Mild Access to Oxazole Derivatives vol.16, pp.3, 2010, https://doi.org/10.1002/chem.200902472
  13. Gold(I)‐Catalyzed Addition of Diphenyl Phosphate to Alkynes: Isomerization of Kinetic Enol Phosphates to the Thermodynamically Favored Isomers vol.122, pp.38, 2005, https://doi.org/10.1002/ange.201001799
  14. Gold(I)‐Catalyzed Addition of Diphenyl Phosphate to Alkynes: Isomerization of Kinetic Enol Phosphates to the Thermodynamically Favored Isomers vol.49, pp.38, 2005, https://doi.org/10.1002/anie.201001799
  15. Gold(I)‐Catalyzed Access to Tetrahydropyran‐4‐ones from 4‐(Alkoxyalkyl)oxy‐1‐butynes: Formal Catalytic Petasis–Ferrier Rearrangement vol.17, pp.5, 2005, https://doi.org/10.1002/chem.201002918
  16. Palladium-Catalyzed Cross-Coupling Reaction and Gold-Catalyzed Cyclization for Preparation of Ethyl 2-Aryl 2,3-Alkadienoates and α-Aryl γ-Butenolides vol.32, pp.8, 2005, https://doi.org/10.5012/bkcs.2011.32.8.2911
  17. Gold-catalyzed oxycyclization of allenic carbamates: expeditious synthesis of 1,3-oxazin-2-ones vol.9, pp.None, 2013, https://doi.org/10.3762/bjoc.9.93
  18. Gold as a catalyst. Part III. Addition to double bonds vol.89, pp.4, 2005, https://doi.org/10.1070/rcr4901
  19. The core of the matter - arene substitution determines the coordination and catalytic behaviour of tris(1-phosphanyl-1′-ferrocenylene)arene gold(I) complexes vol.49, pp.46, 2005, https://doi.org/10.1039/d0dt02743j