309724-93-4Relevant articles and documents
An efficient one pot four-component synthesis of spiro[indoline-3,4′pyrano[2,3-c]pyrazole] derivatives via electrochemical approach
Upadhyay, Abhishek,Singh
, p. 1685 - 1691 (2021/07/02)
An efficient, simple and one pot, synthesis of spiro[indoline-3,4′-pyrano[2,3-c]pyrazole] derivative by electrochemically induced condensation of β-keto ester, hydrazine hydrate, malononitrile or ethyl cyanoacetate and isatin in an undivided cell at const
4-Dimethylaminopyridine-catalyzed multi-component one-pot reactions for the convenient synthesis of spiro[indoline-3,4′-pyrano[2,3-c]pyrazole] derivatives
Feng, Jun,Ablajan, Keyume,Sali, Ahat
supporting information, p. 484 - 489 (2014/01/06)
An efficient and clean reaction process was developed for the convenient and cheap synthesis of spirooxindole derivatives. One-pot reactions of isatins, malononitrile (or ethyl cyanoacetate), hydrazine hydrate (or phenylhydrazine), and 1,3-dicarbonyl comp
A clean and one-pot synthesis of spiroindoline-pyranopyrazoles
Ahadi, Somayeh,Yasaei, Zahra,Bazgir, Ayoob
experimental part, p. 1090 - 1094 (2010/11/03)
(Chemical Equation Presented) Piperidine catalyzes efficiently the one-pot, four-component reaction of β-ketoesters, hydrazine hydrate, malononitrile, and isatines in aqueous media. The reaction was done at room temperature and the spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-5′-carbonitriles were obtained with high yields and purity via an easy work-up procedure. These compounds were also investigated in vitro for antibacterial activities.