Potential anticonvulsants. V. The condensation of isatins with C‐acetyl heterocyclic compounds
- 1 May 1982
- journal article
- research article
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 19 (3) , 589-592
- https://doi.org/10.1002/jhet.5570190327
Abstract
A number of C‐acetyl heterocyclic compounds were condensed with isatin and substituted isatins to give a series of 3‐hydroxy‐3‐substituted oxindoles. The products from 2‐acetylfuran and isatin, 2‐acetylthiophene and isatin, and 2‐acetylpyridine and 1‐methylisatin were active at 100 mg/Kg in the maximal electroshock seizure test.This publication has 2 references indexed in Scilit:
- Synthesis of potential anticonvulsants: Condensation of isatins with acetone and related ketonesJournal of Pharmaceutical Sciences, 1980
- Synthesis of 3-Hydroxy-3-phenacyloxindole AnalogsJournal of Pharmaceutical Sciences, 1979