Abstract
A simple synthesis of novel benzylidenrhodanine based Furan derivatives was described from 5-arylidene 3- carboxymethylrhodanine derivatives via multi-component reactions. The reactive 1:1 intermediate produced from the reaction of tert-butyl isocyanide and dialkyl acetylenedicarboxylates was trapped at room temperature by 5-arylidene 3- carboxymethylrhodanine derivatives to yield polyfunctionalized furan rings in fairly good yields. The products have been analyzed for antibacterial activity against Gram positive and Gram negative bacteria. The results indicated that the synthesized compounds are effective against bacterial growth retardation activity to some extent and their effectiveness is higher for Staphylococcusaureus.
Keywords: Antibacterial activity, Benzylidenrhodanine, Dialkyl acetylenedicarboxylates, tert-butyl isocyanide.
Graphical Abstract
Related Books
Advances in Organic Synthesis
The Synthetic Methods, Structures, and Properties of the Ca-C σ Bond Organocalcium Containing Compounds
Advances in Organic Synthesis
Chemistry of Bipyrazoles: Synthesis and Applications
Advances in Organic Synthesis
Advanced Nanocatalysis for Organic Synthesis and Electroanalysis
Advances in Organic Synthesis
Advances in Organic Synthesis
29