161007-87-0

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 161086-23-3 (3aS,4R,6R,6aS)-4-(2-Benzyloxycarbonylamino-acetylamino)-6-((R)-1,2-dihydroxy-ethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid methyl ester 
• 26198-39-0 1-(N-benzyloxycarbonyl-glycyloxy)-1H-benzotriazole 
• 153796-89-5 (3aS,4S,6R,6aS)-4-Amino-6-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid methyl ester 
• 153796-90-8 (3aS,4R,6R,6aS)-4-Amino-6-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid methyl ester 
• 127903-44-0 2-azido-2-deoxy-3,4:6,7-di-O-isopropylidene-D-glycero-D-talo-heptono-1,5-lactone 
• 128911-23-9 2-azido-2-deoxy-3,4:6,7-di-O-isopropylidene-D-glycero-D-galacto-heptono-1,5-lactone 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 153796-88-4 (3aR,4R,7S,7aR)-7-Amino-4-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-one 
• 153796-92-0 (3aR,4R,7R,7aR)-7-Amino-4-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-one 

Downstream Products

• 161086-23-3 (3aS,4R,6R,6aS)-4-(2-Benzyloxycarbonylamino-acetylamino)-6-((R)-1,2-dihydroxy-ethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid methyl ester 
• 161086-26-6 {[(3aS,4R,6R,6aS)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-4-hydrazinocarbonyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylcarbamoyl]-methyl}-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Spirodiketopiperazines of mannofuranose: Carbopeptoid α-amino acid esters at the anomeric position of mannofuranose

Epimeric mannofuranose anomeric aminoesters are prepared from readily available azidolactones and can act as building blocks for the incorporation of mannofuranose units into peptide chains [carbopeptoids]; alternative acylating conditions allow either ra

TRI- AND TETRA-PEPTIDES INCORPORATING AN α-AMINO ACID AT THE ANOMERIC PROSITION OF MANNOFURANOSE

The first examples of peptides containing an α-amino acid residue in which the α-carbon is also the anomeric position of a carbohydrate are described.