Title of article :
A novel intramolecular Diels–Alder approach to securinega alkaloids: formal synthesis of securinine
Author/Authors :
Honda، نويسنده , , Toshio and Namiki، نويسنده , , Hidenori and Kudoh، نويسنده , , Mika and Watanabe، نويسنده , , Naofumi and Nagase، نويسنده , , Hiromasa and Mizutani، نويسنده , , Hirotake، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2000
Pages :
4
From page :
5927
To page :
5930
Abstract :
A formal total synthesis of securinine (1) was achieved by employing an intramolecular Diels–Alder reaction of the enol ester, derived from 2-acetylpyridine and sorbic anhydride, as a key step.
Keywords :
enol ester , Securinine , Diels–Alder reaction , GABAA receptor antagonist
Journal title :
Tetrahedron Letters
Serial Year :
2000
Journal title :
Tetrahedron Letters
Record number :
1638327
Link To Document :
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