A protected form of title compound 6a, whose two which, after O-silylation, was subjected to iodocyclisation to give 5-iodomethylisoxazolidine 7a as a single diastereo-enantiomers are known to be potent α-glycosidase inhibitors, was obtained through a five-step synthesis based on two isomer. Displac
Biosynthesis of aristeromycln: Evidence for the intermediacy of a 4β-hydroxymethyl-1α, 2α, 3α-trihydroxycyclopentanetriol.
✍ Scribed by Ronald J. Parry; Kochat Haridas; Randall De Jong; Carl R. Johnson
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 238 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Evidence for the intermediacy of a 46-hydroxymethyl-1 a, 2a, 3a+ihydroxycyclopentanetriol (5 or 6) in the biosynthesis of the nucleoside antibiotic aristeromycin (1) has been obtained by administration of doubly-labeled forms of D-glucose to the fermentation broth of Strepfomyces citricolorfollowed by trapping of the tetrol 5 using isotope dilution methods.
📜 SIMILAR VOLUMES
Glycopepfide (I), Neu5A~2-3Gall~l-4GlcNA~l-2Maactl-Ser, was synthesized using a chemoenzymatic strategy. Gal~l-4GlcNAcl~l\*2Man Ifisacd~ide was ~ using glycosidase assisted oligom:x:lutride synthesis. After coupling of this trisacchaxide with a sefine defivstive by chemical glycosylstion, sialic add