ACID-CATALYZED ALPHA-PYRONE RING FORMATION REACTIONS

Date

1994-05-05

Author

Tanyeli, Cihangir
DEMIR, AS
OZARSLAN, O
MECIDOGLU, I
TARHAN, O

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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

Citation Formats

C. Tanyeli, A. DEMIR, O. OZARSLAN, I. MECIDOGLU, and O. TARHAN, “ACID-CATALYZED ALPHA-PYRONE RING FORMATION REACTIONS,” HETEROCYCLES, vol. 37, no. 3, pp. 1705–1715, 1994, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/55548.