Title of article :
Synthesis of 2,3,4,5-tetra-substituted pyrroles via a base-promoted double Michael reaction of oxime-enoates with nitroolefins
Author/Authors :
Kuroda، نويسنده , , Yusuke and Imaizumi، نويسنده , , Kazuto and Yamada، نويسنده , , Ken-ichi and Yamaoka، نويسنده , , Yosuke and Takasu، نويسنده , , Kiyosei، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
3
From page :
4073
To page :
4075
Abstract :
A new method of synthesizing 2,3,4,5-tetra-substituted pyrroles from oxime-enoates with nitroolefins is described. This reaction involves a base-promoted double Michael reaction, followed by dehydrative aromatization.
Keywords :
pyrroles , oximes , Nitroolefins , Domino reaction , Michael addition
Journal title :
Tetrahedron Letters
Serial Year :
2013
Journal title :
Tetrahedron Letters
Record number :
1885070
Link To Document :
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