𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Microbial hydroxylation and functionalization of synthetic bicyclic enones

✍ Scribed by A. Hammoumi; G. Revial; J. D'Angelo; J.P. Girault; R. Azerad


Book ID
104214861
Publisher
Elsevier Science
Year
1991
Tongue
French
Weight
361 KB
Volume
32
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


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.


πŸ“œ SIMILAR VOLUMES


Synthesis and microbial hydroxylation of
✍ Horacio F. Olivo; Michael S. Hemenway; Mikail H. Gezginci πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 332 KB

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.

Selective microbial hydroxylation and bi
✍ Shanghui Hu; Di-an Sun; Xufang Tian; Qicheng Fang πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 French βš– 260 KB

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