143833-86-7

Upstream product

• 143833-83-4 (2S,3R)-2-azido-4-O-(4-methoxybenzyl)butan-1,3,4-triol 
• 143833-81-2 (Z)-4-(4-methoxybenzyloxy)but-2-en-1-ol 
• 74076-63-4 2-(4-methoxyphenyl)-4,7-dihydro-1,3-dioxepine 
• 143833-82-3 (2R,3S)-2,3-epoxy-4-O-(4-methoxybenzyl)butan-1,4-diol 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 143833-99-2 methyl (5S)-5-O-benzyl-5-C-<(2S,5S,6R)-6-(benzyloxy)-5-<(tert-butyldimethylsilyl)oxymethyl>-3,4,5,6-tetrahydro-3-oxo-2H-1,4-diazepin-2-yl>-2,3-O-isopropylidene-β-D-ribofuranoside 
• 143833-87-8 (2S, 3R)-2-amino-3-O-benzyl-1-O-(tert-butyldimethylsilyl)-4-O-(4-methoxybenzyl)butane-1,3,4-triol 

Relevant academic research and scientific papers

STEREOSPECIFIC SYNTHESIS OF A RIBOSYL-DIAZEPANONE DERIVATIVE; A SYNTHETIC APPROACH FOR ELUCIDATION OF THE STEREOCHEMISTRY OF A LIPID NUCLEOSIDE ANTIBIOTIC LIPOSIDOMYCIN B

A new type of ribosyl-diazepanone derivative (23), the core ribosyl 7-membered heterocycle of the nucleoside antibiotic liposidomycin B has been synthesized using a chiral synthetic route that could offer accessibility to any of possible stereoisomers of