213480-41-2

Upstream product

• 301532-85-4 N-(benzyl)-4-(methyl-2,3-O-isopropylidene-4b-D-ribopento-1,4-furanoside)methylene-imine 
• 213480-39-8 (2R,3R,4R,5R)-5-((3'S,4'R)-1-benzyl-3-benzyloxyazetidin-2-one-4-yl)-3,4-dihydroxy-3,4-di-O-isopropylidene-2-methoxytetrahydrofuran 
• 100-46-9 benzylamine 
• 33985-40-9 (3aR,4S,6R,6aR)-tetrahydro-6-methoxy-2,2-dimethylfuro-[3,4-d][1,3]dioxole-4-carbaldehyde 
• 213480-40-1 (2R,3R,4R,5R)-5-((3'S,4'R)-1-benzyl-3-hydroxyazetidin-2-one-4-yl)-3,4-dihydroxy-3,4-di-O-isopropylidene-2-methoxytetrahydrofuran 

Downstream Products

• 213480-45-6 (S)-2-{(S)-2-[(R)-2-Benzylamino-2-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-acetylamino]-4-methyl-pentanoylamino}-4-methyl-pentanoic acid methyl ester 

Relevant academic research and scientific papers

Practical synthesis of α-amino acid N-carboxy anhydrides of polyhydroxylated α-amino acids from β-lactam frameworks. Model studies toward the synthesis of directly linked peptidyl nucleoside antibiotics

A straightforward method for the synthesis of polyhydroxylated α-amino acid N-carboxy anhydrides (NCAs) is described as the means by which short peptide segments comprised of a polyhydroxylated chain are easily affordable. The entire sequence lies in the