Bulletin of the Korean Chemical Society

  • 제23권7호
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  • Pages.998-1002
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  • 2002
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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One-Pot Synthesis of 2H-Pyrans by Indium(III) Chloride-Catalyzed Reactions.Efficient Synthesis of Pyranocoumarins, Pyranophenalenones, and Pyranoquinolinones

  • 발행 : 2002.07.20
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초록

An efficient synthesis of 2H-pyrans is achieved by indium (III) chloride-catalyzed reactions of 1,3-dicarbonyl compounds with a variety of $\alpha\beta-unsaturated$, aldehydes in moderate yields. This method has been applied to the synthesis of pyranocoumar ins, pyranophenalenones, and pyranoquinolinone alkaloids.

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참고문헌

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  3. ChemInform Abstract: One-Pot Synthesis of 2H-Pyrans by Indium(III) Chloride-Catalyzed Reactions. Efficient Synthesis of Pyranocoumarins, Pyranophenalenones, and Pyranoquinolinones. vol.33, pp.48, 2010, https://doi.org/10.1002/chin.200248143
  4. Substituent-Controlled Electrocyclization of 2,4-Dienones: Synthesis of 2,3,6-Trisubstituted 2H-Pyran-5-carboxylates and Their Transformations vol.2011, pp.28, 2011, https://doi.org/10.1002/ejoc.201100780
  5. Efficient synthesis of tetrahydroquinolinones by acetic acid-mediated formal [3+3] cycloaddition vol.143, pp.10, 2012, https://doi.org/10.1007/s00706-012-0762-0
  6. Solvent free l-proline-catalysed domino Knoevenagel/6π-electrocyclization for the synthesis of highly functionalised 2H-pyrans vol.2, pp.21, 2012, https://doi.org/10.1039/c2ra21306k
  7. Catalytic Asymmetric Synthesis of Chromene Derivatives by Iminium Ion Catalysis vol.4, pp.7, 2012, https://doi.org/10.1002/cctc.201200151
  8. ]quinolinones vol.49, pp.6, 2012, https://doi.org/10.1002/jhet.906
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  13. ]quinolones as antiproliferative agents vol.16, pp.12, 2018, https://doi.org/10.1039/C7OB03186F
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  21. Iodine-Catalyzed One-Pot Synthesis of 2H-Pyrans by Domino Knoevenagel/6π-Electrocylization vol.30, pp.11, 2002, https://doi.org/10.5012/bkcs.2009.30.11.2833
  22. Environmentally benign, one-pot synthesis of pyrans by domino Knoevenagel/6π-electrocyclization in water and application to natural products vol.12, pp.11, 2002, https://doi.org/10.1039/c0gc00265h
  23. Green One-Pot Synthesis of 2H-Pyrans Under Solvent-Free Conditions Catalyzed by Ethylenediammonium Diacetate vol.43, pp.2, 2002, https://doi.org/10.1080/00397911.2011.594975
  24. Microwave-Assisted Solvent and Catalyst Free Synthesis of 2H-Pyrans vol.34, pp.10, 2013, https://doi.org/10.5012/bkcs.2013.34.10.2963
  25. Eco-friendly synthesis of fused pyrano[2,3-b]pyrans via ammonium acetate-mediated formal oxa-[3 + 3]cycloaddition of 4H-chromene-3-carbaldehydes and cyclic 1,3-dicarbonyl compounds vol.10, pp.57, 2020, https://doi.org/10.1039/d0ra06450e
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