Bulletin of the Korean Chemical Society

  • 제26권2호
  • /
  • Pages.221-222
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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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Copper(II)-catalyzed Formation of 1,3-Dioxolanes from Oxiranes

  • 발행 : 2005.02.20
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참고문헌

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피인용 문헌

  1. Gold-Catalysed Activation of Epoxides: Application in the Synthesis of Bicyclic Ketals vol.2011, pp.8, 2011, https://doi.org/10.1002/ejoc.201001214
  2. Formation of Five- and Seven-Membered Rings Enabled by the Triisopropylsilyl Auxiliary Group vol.14, pp.1, 2012, https://doi.org/10.1021/ol203209b
  3. Gold(I)-Catalyzed Cyclodehydration Enabled by the Triisopropylsilyl Group: A Synthetically Versatile Methodology vol.95, pp.10, 2012, https://doi.org/10.1002/hlca.201200176
  4. Synthesis, characterization and catalytic evaluation of zirconia-pillared bentonite for 1,3-dioxalane synthesis vol.49, pp.4, 2013, https://doi.org/10.3103/S106837551304011X
  5. Convenient method for the transformation of epoxide to aldehyde and acetonide mediated by Cr-PLM vol.47, pp.4, 2017, https://doi.org/10.1080/00397911.2016.1254799
  6. Copper(II)-Catalyzed Formation of 1,3-Dioxolanes from Oxiranes. vol.36, pp.26, 2005, https://doi.org/10.1002/chin.200526068
  7. A Mild Stereo- and Enantiospecific Conversion of 2,3-Diaryl-Substituted Oxiranes into 2,2-Dimethyl-1,3-Dioxolanes by an Acetone/Amberlyst 15 System vol.2006, pp.13, 2006, https://doi.org/10.1002/ejoc.200600034
  8. A Microwave-Enhanced, Lewis Acid-Catalyzed Synthesis of 1,3-Dioxolanes and Oxazolines from Epoxides vol.349, pp.7, 2007, https://doi.org/10.1002/adsc.200600516
  9. Highly efficient Meinwald rearrangement reactions of epoxides catalyzed by copper tetrafluoroborate vol.47, pp.33, 2005, https://doi.org/10.1016/j.tetlet.2006.06.055
  10. Copper(II) tetrafluroborate-promoted Meinwald rearrangement reactions of epoxides vol.66, pp.43, 2010, https://doi.org/10.1016/j.tet.2010.08.078