124288-79-5

Upstream product

• 124288-78-4 1,1-dimethylethyl amino>-2,3-O-(1-methylethylidene)-β-D-ribo-dec-5-enofuranosid>uronates 
• 124288-76-2 (S)-6-Hydroxy-6-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-nitro-2-(toluene-4-sulfonylamino)-hexanoic acid tert-butyl ester 
• 124288-77-3 1,1-dimethylethyl amino>-2,3-O-(1-methyl-ethylidene)-β-D-ribo-dec-5-enofuranosid>uronates 
• 124288-73-9 1,1-dimethylethyl (S)-2-<<(4-methylphenyl)sulfonyl>-amino>-5-<<(phenylmethoxy)carbonyl>amino>pentanoate 
• 110414-90-9 α-N-tosyl-δ-N-carbobenzoxyornthine 
• 124288-75-1 1,1-dimethylethyl (S)-5-nitro-2-<<(4-methylphenyl)sulfonyl>amino>pentanoate 
• 124288-74-0 1,1-dimethylethyl (S)-5-amino-2-<<(4-methylphenyl)sulfonyl>-amino>pentanoate 
• 33985-40-9 (3aR,4S,6R,6aR)-tetrahydro-6-methoxy-2,2-dimethylfuro-[3,4-d][1,3]dioxole-4-carbaldehyde 

Relevant academic research and scientific papers

Stereoselective Synthesis and Absolute Stereochemistry of Sinefungin

Sinefungin has been synthesized from D-ribose, L-ornithine, and adenine.L-Ornithine was converted to its δ-nitro analogue 10, which was coupled to the ribose derived aldehyde 11 by a potassium fluoride catalyzed nitro-aldol reaction.The resulting nitro al