Synthesis of tetrasubstituted thiophenes on solid-support using the Gewald reaction
β Scribed by Georgette M Castanedo; Daniel P Sutherlin
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 107 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The Gewald reaction was performed on solid support. This reaction combines a ketone or aldehyde, an activated nitrile, and sulfur in the presence of a suitable amine base to make tri-and tetrasubstituted thiophenes. After optimizing conditions for maximum yield and purity, the scope of the reaction was investigated. Finally, this method is highlighted in the synthesis of two biologically relevant compounds.
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Solid phase intramolecularHeck couplingallows the syothesisof 2-oxindoles. Additional diversityis introducedinfo the moleculeby reductiveatkylationprior to the Heck cyclisationarrdatso by conjugateadditionof a varietyof nucleophilesontothe cyctisedproductprior to cleavage. 01997 Elsevier ScienceLtd.