700819-48-3

Upstream product

• 115141-23-6 1-deoxy-1-diethylmethylsilyloxymethyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 247167-07-3 N-(o-nitrobenzenesulfonyl)-L-phenylalanine tert-butyl ester 
• 561017-53-6 1-deoxy-1-hydroxymethyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 

Downstream Products

• 700819-57-4 (S)-2-[((3aS,4S,6R,6aR)-6-{[((S)-1-tert-Butoxycarbonyl-ethyl)-(2-nitro-benzenesulfonyl)-amino]-methyl}-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl)-(2-nitro-benzenesulfonyl)-amino]-3-phenyl-propionic acid allyl ester 
• 700819-61-0 (S)-2-[((3aS,4S,6R,6aR)-6-{[((S)-1-tert-Butoxycarbonyl-ethyl)-(2-nitro-benzenesulfonyl)-amino]-methyl}-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl)-(2-nitro-benzenesulfonyl)-amino]-3-phenyl-propionic acid 
• 700819-53-0 (S)-2-[((3aS,4S,6R,6aR)-6-Hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl)-(2-nitro-benzenesulfonyl)-amino]-3-phenyl-propionic acid allyl ester 

Relevant academic research and scientific papers

Novel reversed chain modified oligopeptides via sequential α-N-mitsunobu condensation of a functionalized C-glycoside

The synthesis of a novel reversed chain modified oligopeptide via sequential α-N-Mitsunobu condensation reactions on a C-glycoside with amino acid derived nitrobenzenesulfonamides is described. Structural analysis of the target compound 11 using NMR techn