| Literature DB >> 10782697 |
R Larget1, B Lockhart, P Renard, M Largeron.
Abstract
A series of 8-alkylamino-5,7-dihydroxyflavones was prepared from chrysine via a seven step sequence. The synthesis of their 6-alkylamino isomers could be subsequently accomplished through a convenient extension of the Wessely-Moser rearrangement. These compounds were found to be efficient neuroprotective agents in vitro.Entities:
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Year: 2000 PMID: 10782697 DOI: 10.1016/s0960-894x(00)00110-4
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823