258872-97-8

Upstream product

• 102770-00-3 1-[5-O-[4,6-dideoxy-6-oxo-6-[[[(3S)-hexahydro-2-oxo-1H-azepine]-3-yl]amino]-β-L-erythro-4-hexenopyranosyl]-3-O-methyl 6-deoxy-6-amino-α-L-talofuranuronosyl]-1,2,3,4-tetrahydro-2,4-dioxopyrimidine 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 1005-56-7 phenylcarbonochloridothioate 
• 258872-96-7 4-(tert-butyl-dimethyl-silanyloxy)-6-{[4-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-methoxy-tetrahydro-furan-2-yl]-carbamoyl-methoxy}-5-hydroxy-5,6-dihydro-4H-pyran-2-carboxylic acid (2-oxo-azepan-3-yl)-amide 

Relevant academic research and scientific papers

Novel intramolecular radical Ar-C glycosylation-lactonization reaction in the transformation of capuramycin

Radical deoxygenation of capuramycin derivative (2a,b) gave the unexpected lactone (3a,b) in moderate yield via a novel intramolecular radical Ar-C glycosylation-lactonization reaction. R-115381 and R-116022, thus obtained, showed weak antimicrobial activ