Article ID Journal Published Year Pages File Type
5276412 Tetrahedron Letters 2007 4 Pages PDF
Abstract
3,5,6-Trisubstituted α-pyrones were synthesized starting from the Baylis-Hillman adducts. The synthesis was carried out via the sequential introduction of ketone at the primary position of Baylis-Hillman adduct, lactonization, and the following oxidation with PCC.
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Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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Synthesis of 3,5,6-trisubstituted α-pyrones from Baylis-Hillman adducts
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