Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5222484 | Tetrahedron | 2009 | 6 Pages |
Abstract
An expeditious transformation of 5-acyl-2H-pyran-2-ones with various amidines as 1,3-binucleophiles into isomerically pure (E)-α,β-didehydro-α-amino acid derivatives (DDAAD) containing the 5-pyrimidyl moiety at the β-position is described. The method was performed in ethanolic (or ethanol/water) solutions in the presence of Na2CO3 as a nontoxic base and under microwave-assisted conditions. When starting from the 5-ethoxycarbonyl-2H-pyran-2-one derivative and in the presence of DBU as a base the corresponding pyrano[2,3-d]pyrimidines were prepared.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jure Hren, Franc Požgan, Alma BuniÄ, Vasile I. Parvulescu, Slovenko Polanc, Marijan KoÄevar,