Engaging isatins in solvent-free, sterically congested Passerini reaction
Literature Information
Trinadh Kaicharla, Santhivardhana Reddy Yetra, Tony Roy, Akkattu T. Biju
A facile, atom-economic and environmentally-benign protocol for the synthesis of biologically important oxindole derivatives in high yields has been demonstrated by employing isatins as carbonyl compound surrogates in a Passerini reaction carried out under solvent-free conditions. Moreover, electron-deficient phenols can also be used as the acid component in this reaction. In addition, the synthetic utility of the present methodology was examined by the one-pot synthesis of oxindoles with a free –OH group at the benzylic position.
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