Microbial hydroxylation and functionalization of hydrindenones
โ Scribed by Virginie Goubaud; Abderrahmane Hammoumi; Jean-Pierre Girault; Gilbert Revial; Jean d'Angelo; Robert Azerad
- Book ID
- 103977308
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 546 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0957-4166
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๐ SIMILAR VOLUMES
The reglo-and stereoselective hydroxylation of substituted octalones by various fungal strams has been evaluated. Several hydroxylated derivatives have been obtained and the potential of this method for the preparation of useful cblral synthons is discussed.
heptanes have been synthesized in a short route. These compounds containing benzamide or benzenesulfonamide groups are good substrates for microbial oxidation of unactivated carbons by B. bassiana.
Sct,7[3,9ct, 1013,13ct-Pentaacetoxy-4(20) . l 1-taxadiene I was selectively transformed into its l[3,14[3-hydroxylated derivatives 2, 3, and 1 l(15~.l)abeotaxane 4 by different filamentous fungi. Microbial transformation of a series of taxoids with a 4(20) exocyclic double bond was described. The m