75307-57-2Relevant academic research and scientific papers
Synthetic aci-Reductones: 3,4-Dihydroxy-2H-1-benzopyran-2-ones and Their cis- and trans-4a,5,6,7,8,8a-Hexahydro Diastereomers. Antiaggregatory, Antilipidemic, and Redox Properties Compared to Those of the 4-Substituted 2-Hydroxytetronic Acids
Witiak, Donald T.,Kim, Sung K.,Tehim, Ashok K.,Sternitzke, Kent D.,McCreery, Richard L.,et al.
, p. 1437 - 1445 (2007/10/02)
Synthetic procedures for the elaboration of aci-reductones belonging to the 6- or 7-mono- or bis-substituted-3,4-dihydroxy-2H-1-benzopyran-2-ones (6 - 10) and their cis- and trans-4a,5,6,7,8,8a-hexahydro diastereomers (11, 12) are described.Hexahydrobenzo
Introduction of Oxygen Functions into the α-Position of β-Diketones, 4: "Hydroxy- and Oxo-Meldrum's Acids"
Bouillon, Guenther,Schank, Kurt
, p. 2630 - 2635 (2007/10/02)
Synthesis and properties of 5-hydroxy-, 5-acyloxy-, 5-oxo- and 5,5-dihydroxy-2,2-dialkyl-1,3-dioxane-4,6-diones (6, 5/9, 7, 10) are described.
