403737-17-7

Upstream product

• 362054-97-5 Benzoic acid 1-(ethoxycarbonyl-methylamino-methyl)-allyl ester 
• 403737-16-6 (2R,3S)-2-Azido-3-[(3aR,5R,6R,6aR)-6-(tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-3-hydroxy-propionic acid 
• 403737-34-8 (2S,3R)-3-[(3aR,5R,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-oxirane-2-carboxylic acid 
• 403737-15-5 {(2R,3S)-3-[(3aR,5R,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-oxiranyl}-methanol 
• 403737-14-4 (E)-3-[(3aR,5R,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-acrylic acid methyl ester 
• 403737-33-7 (5E)-3-O-[(tert-butyl)dimethylsilyl]-5,6-dideoxy-1,2-O-isopropylidene-α-D-ribo-hept-5-enofuranose 
• 403737-32-6 (3aR,5S,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole-5-carbaldehyde 
• 403737-31-5 3-O-[(tert-butyl)dimethylsilyl]-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 226943-69-7 1,2-O-isopropylidene-3-O-(tert-butyldimethylsilyl)-α-D-allofuranose 
• 2595-05-3 Diacetone D-glucose 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Relevant academic research and scientific papers

Synthesis of the liposidomycin diazepanone nucleoside

(formula presented) The synthesis of the liposidomycin degradation product 4 from D-glucose establishes its stereochemistry as 5′S,6′S and, by incorporation of the earlier diazepanone relative stereochemical assignment, establishes the absolute stereochem