The synthesis of hemiaminal of indole is described by the reaction of indole with formaldehyde in the presence of TBAF in water at ambient temperature. The procedure is very efficient, mild, convenient, and environmentally benign with high yield of product. Moreover, the reuse of reaction media makes the procedure an attractive alternative to earlier methods.
An efficient Henry reaction has been described for the synthesis of 3-hydroxy-3-(nitroalkyl)-2-oxindole by the reaction of isatins with nitroalkanes in N,N-dimethylformamide (DMF) under anhydrous condition. This method provides high yield of 3-hydroxy-2-oxindoles under mild reaction condition. Moreover, the procedure is environmentally benign in nature, efficient, and applicable to variety of isatins as well as nitroalkanes.
A DABCO catalyzed, novel and efficient one-pot, four component protocol has been developed for the synthesis of (Z)-5-(3-hydroxy-2-oxoindolin-3-yl)-2-iminothiazolidin-4-one scaffolds under metal-free conditions.
The reaction is conducted under metal‐free conditions and gives a wide range of the title compounds by using simple and readily available starting materials.
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