66623-50-5Relevant academic research and scientific papers
Aqueous single step synthesis and structural characterization of allylated, propargylated, and benzylated 3-substituted 3-aminooxindoles
Karpe, Sameer A.,Singh, Man,Chowhan, L. Raju
supporting information, p. 1737 - 1746 (2017/09/23)
Efficient zinc-mediated allylation, propargylation, and benzylation of isatin-derived imines were undertaken for the synthesis of 3-substituted 3-aminooxindoles with ≈80% yield. Such alternative approach has efficiently avoided the use of catalysts, sever
Synthesis and antibacterial screening of hydrazones, Schiff and Mannich bases of isatin derivatives
Sridhar, Seshaiah Krishnan,Saravanan, Muniyandy,Ramesh, Atmakuru
, p. 615 - 625 (2007/10/03)
Schiff bases and hydrazones of substituted isatins (1-28) were prepared by reacting isatin and aromatic primary amines/hydrazines. A new series of the corresponding N-Mannich base (29-35) was synthesised by reacting them with formaldehyde and diphenyl ami
Synthesis and pharmacological activities of hydrazones, schiff and mannich bases of isatin derivatives
Sridhar, Seshaiah Krishnan,Ramesh, Atmakuru
, p. 1149 - 1152 (2007/10/03)
Schiff bases and phenyl hydrazone of isatins were prepared by reacting isatin and the appropriate aromatic primary amine/hydrazines. A new series of the corresponding N-mannich bases were synthesized by reacting them with formaldehyde and diphenylamine. T
Reactions of 3-Arylimino-2-Indolinones with p-Substituted Phenylthiosemicarbazides
Varma, Rajendra S.,Garg, Pradeep K.
, p. 980 - 981 (2007/10/02)
3-Arylimino-2-indolinones (II) have been prepared by the condensation of isatins (I) with anilines.Reactions of II with p-substituted phenylthiosemicarbazides have resulted (in every instance) in the displacement of arylimino groups by the phenylthiosemic
