Title of article
A convenient extension of the Wessely–Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro
Author/Authors
Ronan Larget، نويسنده , , Brian Lockhart، نويسنده , , Pierre Renard، نويسنده , , Martine Largeron، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2000
Pages
4
From page
835
To page
838
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.
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
2000
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
790747
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