Title of article :
Simple stepwise route to 1-substituted 2-amino-3-ethoxycarbonylindolizines
Author/Authors :
Gennadiy E. Khoroshilov، نويسنده , , Natalia M. Tverdokhleb، نويسنده , , Vladimir S. Brovarets، نويسنده , , Eugene V. Babaev، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
5
From page :
4353
To page :
4357
Abstract :
2-Chloro-N-ethoxycarbonylmethylpyridinium bromide reacts with substituted acetonitriles in two steps; the initially formed pyridine anhydro baseses undergo further ring closure to 2-amino-3-ethoxycarbonylindolizines.
Keywords :
2-Aminoindolizine , 2-Chloro-Nethoxycarbonylmethylpyridinium bromide , Pyrrole ring synthesis , CH-acids
Journal title :
Tetrahedron
Serial Year :
2013
Journal title :
Tetrahedron
Record number :
1105794
Link To Document :
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