129077-21-0

Upstream product

• 17791-36-5 methyl 2,3-di-O-benzyl-α-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 7177-79-9 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 3162-96-7 methyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 7177-79-9 methyl 2,3-O-dibenzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 

Downstream Products

• 273720-68-6 N-benzyl-2,3-di-O-benzyl-6-chloro-1,5,6-trideoxy-1,5-imino-L-iditol 
• 129077-22-1 (2S,3S,4S)-1-Benzyl-3,4-bis-benzyloxy-2-vinyl-pyrrolidine 
• 129077-31-2 (S)-1-((2S,3S,4S)-1-Benzyl-3,4-bis-benzyloxy-pyrrolidin-2-yl)-ethane-1,2-diol 
• 129077-30-1 (R)-1-((2S,3S,4S)-1-Benzyl-3,4-bis-benzyloxy-pyrrolidin-2-yl)-ethane-1,2-diol 
• 273720-69-7 N-benzyl-2,3-di-O-benzyl-1,5,6-trideoxy-1,5-imino-D-gluco-heptitol 
• 273720-70-0 N-benzyl-2,3-di-O-benzyl-1,5,6-trideoxy-1,5-imino-L-ido-heptitol 
• 273720-65-3 3,7-anhydro-2,7-dideoxy-N-benzyl-5,6-di-O-benzyl-3,7-imino-L-gulo-1,4-heptonolactone 
• 273720-66-4 3,7-anhydro-2,7-dideoxy-N-benzyl-5,6-di-O-benzyl-3,7-imino-L-ido-1,4-heptonolactone 
• 129170-93-0 (2S,3S,4R)-N-Benzyl-2,3-di-O-benzyl-2,3,4-trihydroxyhex-5-enylamine 

Relevant academic research and scientific papers

Structure and reactions of glycopyranoside derived dialdehydes

Several 4- protected D-glucopyranosides were synthesized and cleaved by sodium metaperiodate. Depending on the protection pattern the resulting dialdehydes showed different types of structures. Predominantly dioxane structures of the hemiacetal or hemiald

Total synthesis of new C-6 homologues of 1-deoxynojirimycin and 1-deoxy- L-idonojirimycin

Novel piperidine lactones 1 and 2, which represent direct precursors to the new C-6 homologues of 1-deoxynojirimycin (3) and 1-deoxy-L-donojirimycin 4, were prepared by key Pd(II)-catalysed aminocarbonylation of protected aminoalkene 10.

Halogenation of carbohydrates by triphenylphosphine complex reagents in highly concentrated solution under microwave activation or conventional heating

Halogenation of carbohydrates with triphenylphosphine and carbon tetrachloride, hexachloroethane or 1,2-dibromotetrachloroethane was shown to be very efficient in highly concentrated solutions of nonpolar solvents such as toluene or 1,2-dichloroethane, wi

A SHORT, VERSATILE APPROACH TO POLYHYDROXYLATED PYRROLIDINES UTILIZING A REDUCTIVE ELIMINATION-REDUCTIVE AMINATION AS A KEY STEP

An efficient synthesis of epimeric alpha-vinyl pyrrolidines starting from methyl 4,6-O-benzyliden gluco- and galactopyranosides gave ready access to hydroxylated pyrrolidines.