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Benzoin Condensation Reactions of 5-Membered Heterocyclic Compounds Catalyzed by Thiazolium Salts

  • Chang Kiu Lee (Department of Chemistry, Kangweon National University) ;
  • Jin Soon Gong (Department of Chemistry, Kangweon National University) ;
  • Sin Kwan Seog (Department of Pharmacy, Kangweon National University) ;
  • Jong-Gab Jun (Department of Chemistry, Hallym University)
  • Published : 1993.02.20

Abstract

Benzoin condensation reactions of furfurals and thiophenecarboxaldehydes in the presence of substituted benzyl and alkyl thiazolium salts were examined in order to improve the yield of the reaction and to examine the effect of the electronic nature of the catalysts. Thiophene derivatives gave thenils as the major products in low yields while furan derivatives gave only furoins in moderate to high yields.

Keywords

References

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Cited by

  1. ChemInform Abstract: Benzoin Condensation Reactions of 5-Membered Heterocyclic Compounds Catalyzed by Thiazolium Salts. vol.24, pp.46, 1993, https://doi.org/10.1002/chin.199346079
  2. Polymer Supported Cyanide as an Efficient Catalyst in Benzoin Condensation: An Efficient Route to α-Hydroxy Carbonyl Compounds vol.30, pp.5, 2009, https://doi.org/10.5012/bkcs.2009.30.5.1164