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Silicon tetrachloride catalyzed aza-michael addition of amines to conjugated alkenes under solvent-free conditions

Azizi, N ; Sharif University of Technology

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  1. Type of Document: Article
  2. DOI: 10.1055/s-0029-1219195
  3. Abstract:
  4. The efficient and very simple conjugate addition of aromatic and aliphatic amines to α,β-unsaturated carbonyl compounds under solvent-free conditions in the presence of catalytic amount of silicon tetrachloride is reported. The reaction of aryl and alkyl amines with different Michael acceptors gave the corresponding Michael adducts with simple catalyst and good to excellent yields
  5. Keywords:
  6. Aminocarbonyl compounds ; Aromatic amine ; Conjugate addition ; Silicon tetrachloride ; Alkene derivative ; Alkyl group ; Amine ; Carbonyl derivative ; Polycyclic aromatic hydrocarbon derivative ; Silicon ; Solvent ; Article ; Catalysis ; Catalyst ; Conjugation ; Michael addition ; Quantum yield ; Reaction analysis
  7. Source: Synlett ; Issue 3 , 2010 , Pages 379-382 ; 09365214 (ISSN)
  8. URL: https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0029-1219195