Title of article
Tandem in situ Generation of Azomethine Ylides and Base Sensitive Nitroethylene Dipolarophiles
Author/Authors
Imre Fejes، نويسنده , , L?szl? T?ke، نويسنده , , Mikl?s Nyerges، نويسنده , , Chwang Siek Pak، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
6
From page
639
To page
644
Abstract
We have studied the behaviour of 2-acetoxy-nitroethane derivatives in the presence of triethylamine and of an azomethine ylide generated also by the action of this base in the same reaction mixture. Under these conditions the nitro-olefins are generated and react in situ with the corresponding dipoles, giving pyrrolidine derivatives in moderate to good yields.
Keywords
Cycloadditions , Pyrrolidines , Nitro compounds
Journal title
Tetrahedron
Serial Year
2000
Journal title
Tetrahedron
Record number
1080532
Link To Document