Journal of Medicinal Chemistry p. 1437 - 1445 (1988)
Update date:2022-09-26
Topics:
Witiak, Donald T.
Kim, Sung K.
Tehim, Ashok K.
Sternitzke, Kent D.
McCreery, Richard L.
et al.
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
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