Bulletin of the Korean Chemical Society

  • 제25권12호
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  • Pages.1924-1928
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  • 2004
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Zinc Mediated Barbier Type Allylation of Cyclic Imides and Subsequent Coupling Reactions with Carbon Nucleophiles

  • 발행 : 2004.12.20
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초록

Allylations of N-benzyl and N-methyl cyclic imides were accomplished successfully under mild Barbier type conditions using zinc metal, allyl bromide and catalytic amount of $PbBr_2$. Subsequent coupling reactions with some carbon nucleophiles afforded 1,2- and 1,4-addition products in moderate to high yields.

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참고문헌

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  1. Ruthenium-catalyzed intramolecular metathesis of dienes and its application in the synthesis of bridged and spiro azabicycles vol.84, pp.7, 2015, https://doi.org/10.1070/RCR4478
  2. Zinc Mediated Barbier Type Allylation of Cyclic Imides and Subsequent Coupling Reactions with Carbon Nucleophiles. vol.36, pp.22, 2005, https://doi.org/10.1002/chin.200522112
  3. Efficient Synthesis of Spirolactams by Ring-Closing Olefin Metathesis vol.27, pp.1, 2004, https://doi.org/10.5012/bkcs.2006.27.1.153
  4. Metal-Mediated Diastereoselective Allylation Reaction of Chiral α,β-Epoxy Aldehyde. Part 1 vol.27, pp.10, 2006, https://doi.org/10.5012/bkcs.2006.27.10.1519
  5. Cyclization of N-Allyl-5-allyl-5-hydroxylactams to 8a-Hydroxy-1,5,8,8a-tetrahydro-2H-indolizin-3-ones Using Grubbs' Catalyst vol.29, pp.4, 2004, https://doi.org/10.5012/bkcs.2008.29.4.755
  6. A Convenient Synthesis of Polycyclic γ-Lactams via Pauson-Khand Reaction vol.30, pp.3, 2004, https://doi.org/10.5012/bkcs.2009.30.3.691