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- W2031569657 abstract "The action of NaBH4 on some typical isoflavones yields isoflavan-4-ols in 70–85% yields. 2-Methylisoflavones are resistant to this reduction. The isoflavan-4-ols undergo dehydration to isoflavens in presence of protonic reagents suggesting a quasi-trans relationship between the quasi-equatorial 4-OH and 3-H, proposed by Michelie et al.3 and based on NMR evidence." @default.
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- W2031569657 date "1965-01-01" @default.
- W2031569657 modified "2023-09-24" @default.
- W2031569657 title "Synthesis and study of isoflavan-4-ols" @default.
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- W2031569657 doi "https://doi.org/10.1016/s0040-4020(01)93923-7" @default.
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