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Abstract: Recyclable Ni-nanoparticles provides an efficient, economic and rapid method for catalyzing Knoevenagel condensation of aldehydes with an active methylene compound at room temperature. The method offers high yield preferably in case of aromatic aldehydes and proceed well in neutral medium. This method provides a wide range of substrate applicability and simple workup procedure. The products need no further purification and the process is environmentally benign. [Copyright &y& Elsevier]

Abstract: A simple, efficient, stereoselective, one pot three component condensation reaction between thiazolidine-2,4-dione, aldehyde and amine derivatives using monodispersed, recyclable and inexpensive Cu-nanoparticles for the synthesis of thiazolidine-2,4-dione derivatives in excellent yields and high purity has been described here for the first time. [Copyright &y& Elsevier]

Abstract: A novel method for reduction of aromatic and heteroaromatic aldehydes with ammonium formate using Ni-nanoparticles is described. The Ni-nanoparticles act as a green catalyst for selective reduction of the aldehydic group in the presence of other functional groups, viz.: –NO2, –CN and alkenes to give the corresponding alcohols in excellent yields. [Copyright &y& Elsevier]

Abstract: Aldehydes and mercaptoacetic acid are coupled in the presence of a catalytic amount of economical and non-toxic molecular iodine in [bmim][BF4] ionic liquid under mild conditions to afford the corresponding 1,3-oxathiolan-5-one in excellent yields. Molecular iodine acts faster in ionic liquids when compared to conventional solvents such as DMSO, DMF, ethyl acetate, and acetonitrile. The recovered ionic liquids can be recycled in subsequent reactions with consistent activity. [Copyright &y& Elsevier]