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ACID-CATALYZED ALPHA-PYRONE RING FORMATION REACTIONS
Date
1994-05-05
Author
Tanyeli, Cihangir
OZARSLAN, O
MECIDOGLU, I
TARHAN, O
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Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
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The reaction of 1,3-dicarbonyl compounds with methyl 2-carbomethoxy-3-(N-methylanilino)acrylate under acidic condition directly gives substituted 2H-pyran-2-ones in good yield.
Subject Keywords
Efficient Synthesis
,
2h-Pyran-2-One Derivatives
,
Cardioactive Steroids
,
Bufalin
URI
https://hdl.handle.net/11511/55548
Journal
HETEROCYCLES
Collections
Department of Chemistry, Article
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A bis-Lewis basic 2-aminoDMAP/prolinamide organocatalyst for application to the enantioselective synthesis of Warfarin and derivatives
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BibTeX
C. Tanyeli, O. OZARSLAN, I. MECIDOGLU, and O. TARHAN, “ACID-CATALYZED ALPHA-PYRONE RING FORMATION REACTIONS,”
HETEROCYCLES
, pp. 1705–1715, 1994, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/55548.