Title of article :
A direct entry to substituted piperidinones from α,β-unsaturated amides by means of aza double Michael reaction
Author/Authors :
Takasu، نويسنده , , Kiyosei and Nishida، نويسنده , , Naoko and Ihara، نويسنده , , Masataka، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2003
Pages :
4
From page :
7429
To page :
7432
Abstract :
An intermolecular aza-double Michael reaction has been developed leading to functionalized piperidin-2-ones from simple starting materials. The method allows to utilize α,β-unsaturated amides as a synthon of piperidine nucleus. The short synthesis of anti-depressant paroxetine was demonstrated by using the new methodology.
Keywords :
unsaturated amides , Anti-depressant , Heterocycles , piperidines , 1 , 4-additions , domino reactions
Journal title :
Tetrahedron Letters
Serial Year :
2003
Journal title :
Tetrahedron Letters
Record number :
1654821
Link To Document :
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