61294-08-4Relevant academic research and scientific papers
Improved one-pot synthesis of 3-spiro indolines under microwave irradiation
Dandia, Anshu,Saha, Mitali,Taneja, Harshita
, p. 77 - 85 (1998)
The potential of the domestic microwave oven has been utilized to accelerate the one-pot synthesis of spiro[indole-thiazolidine]diones and spiro[indole-benzothiazine]diones by condensation of substituted indole-2,3-diones (1) and appropriate anilines (2)
Synthesis of 1′-aryl-2′-(2-oxoindolin-3-yl)spiro[indoline-3, 5′-pyrroline]-2,3′-dione via one-pot reaction of arylamines, acetone, and isatins
Sun, Yan,Sun, Jing,Yan, Chao-Guo
supporting information; experimental part, p. 3647 - 3649 (2012/09/22)
An efficient synthetic method for 1′-aryl-2′-(2-oxoindolin-3- yl)spiro[indoline-3,5′-pyrroline]-2,3′-diones was successfully developed via the one-pot domino reaction of arylamines, acetone, and isatins in acetic acid. The reaction mechanism involved the
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
