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

DOI: 10.1021/jm00402a032

Source and publish data:

Journal of Medicinal Chemistry p. 1437 - 1445 (1988)

Update date:2022-09-26

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Authors:

Witiak, Donald T.

Kim, Sung K.

Tehim, Ashok K.

Sternitzke, Kent D.

McCreery, Richard L.

et al. et al.

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Article abstract of DOI:10.1021/jm00402a032

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

Full text of DOI:10.1021/jm00402a032

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