Green chemistry approaches to the Knoevenagel condensation: comparison of ethanol, water and solvent free (dry grind) approaches
- 20 March 2002
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 43 (17) , 3117-3120
- https://doi.org/10.1016/s0040-4039(02)00480-x
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Base-promoted reactions in ionic liquid solvents. The Knoevenagel and Robinson annulation reactionsTetrahedron Letters, 2001
- A stereoselective route to 3-methyl-2-methylsulfanyl-5-ylidene-3,5-dihydroimidazol-4-one derivatives and precursor of Leucettamine BGreen Chemistry, 2001
- Solvent-Free Microwave Enhanced Knoevenagel Condensation of Ethyl Cyanoacetate with AldehydesSynthetic Communications, 1999
- Green chemistry: challenges and opportunitiesGreen Chemistry, 1999
- Tyrphostins. 6. Dimeric Benzylidenemalononitrile Tyrphostins: Potent Inhibitors of EGF Receptor Tyrosine Kinase in VitroJournal of Medicinal Chemistry, 1996