| Literature DB >> 438986 |
Abstract
Substituted isatins and substituted acetophenones were condensed to give analogs of 3-hydroxy-3-phenacyloxindole. These alcohols were dehydrated, and the alkene was reduced. None of the products had the level of anticonvulsant activity exhibited by the parent compound.Entities:
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Year: 1979 PMID： 438986 DOI： 10.1002/jps.2600680437
Source DB: PubMed Journal: J Pharm Sci ISSN： 0022-3549 Impact factor: 3.534