Title of article
An efficient synthesis of 2-amino-3-cyano-2-pyrrolin-4-ones, via the corresponding open chain tautomers (aminoacetylmalononitriles)
Author/Authors
Hamilakis، نويسنده , , Stylianos and Tsolomitis، نويسنده , , Athanase، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2003
Pages
3
From page
3821
To page
3823
Abstract
Malononitrile has been found to be acylated effectively using N-protected glycines by simultaneous activation of an amino acid carbonyl group and a malononitrile methylene group using carbonyl diimidazole (CDI). The corresponding aminoacetonitriles were isolated as enols and/or as their tautomeric forms, 2-amino-3-cyano-2-pyrrolin-4-ones.
Keywords
2-amino-3-cyano-2-pyrrolin-4-ones , aminoacetylmalononitriles , tautomers , CDI
Journal title
Tetrahedron Letters
Serial Year
2003
Journal title
Tetrahedron Letters
Record number
1662074
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