78841-76-6

Upstream product

• 7057-10-5 1,2-O-isopropylidene-α-D-5-deoxyglucurono-6,3-lactone 
• 111651-69-5 (3aR,6R,6aR)-6-Hydroxy-5-methoxy-tetrahydro-furo[3,2-b]furan-2-one 
• 111651-70-8 (3aR,6R,6aS)-6-Benzyloxy-5-methoxy-tetrahydro-furo[3,2-b]furan-2-one 
• 78841-75-5 methyl 2,3-anhydro-5-O-benzyl-α-L-gulofuranoside 
• 64243-86-3 6-deoxy-1,2-O-isopropylidene-3-O-(methylsulfonyl)-β-L-idofuranose 
• 100-39-0 benzyl bromide 
• 78841-81-3 methyl 3,5,6-tri-O-benzoyl-2-O-p-tolylsulfonyl-β-D-glucofuranoside 
• 6339-03-3 O³,O⁵,O⁶-tribenzoyl-O¹,O²-isopropylidene-α-D-glucofuranose 
• 78841-70-0 5-O-benzyl-6-deoxy-1,2-O-isopropylidene-β-L-idofuranose 
• 78841-86-8 methyl 2,3-anhydro-6-deoxy-α-L-gulofuranoside 
• 78841-69-7 5-O-benzyl-6-deoxy-1,2-O-isopropylidene-3-(2-phenethylsulfonyl)-β-L-idofuranose 
• 78841-71-1 3-O-benzoyl-5-O-benzyl-6-deoxy-1,2-O-isopropylidene-β-L-idofuranose 
• 78841-68-6 5-O-benzyl-6-deoxy-1,2-O-isopropylidene-3-O-(methylsulfonyl)-β-L-idofuranose 
• 78841-83-5 methyl 2,3-anhydro-6-O-benzoyl-β-D-mannofuranoside 

Downstream Products

• 78841-77-7 methyl 5-O-benzyl-2,6-dideoxy-3-O-(methylsulfonyl)-α-L-lyxo-hexofuranoside 
• 78841-78-8 methyl 3-azido-5-O-benzyl-2,3,6-trideoxy-α-L-lyxo-hexofuranoside 
• 78841-80-2 methyl 3-acetamido-5-O-benzyl-2,3,6-trideoxy-α-L-lyxo-hexofuranoside 
• 78841-79-9 methyl 3-amino-5-O-benzyl-2,3,6-trideoxy-α-L-lyxo-hexofuranoside 
• 78841-77-7 Methanesulfonic acid (2R,3R)-2-((S)-1-benzyloxy-ethyl)-5-methoxy-tetrahydro-furan-3-yl ester 

Relevant academic research and scientific papers

TOTAL SYNTHESIS OF METHYLFURANOSIDES OF 2-DEOXYPENTOSES AND 2,6-DIDEOXYHEXOSES. USE OF 1H AND 13C NMR SPECTROSCOPY TO DETERMINE THE STRUCTURE OF THE GLYCOSIDES OF 2-DEOXY SUGARS

The optimum results during the cyclization of the acyclic acetals of 2-deoxypentoses and 2,6-dideoxyhexoses are obtained when the reaction is conducted in a 0.01-0.05percent solution of hydrogen chloride in methanol at 20 deg C.Under these conditions cycl

SYNTHESIS OF 3-AMINO-2,3,6-TRIDEOXY-L-lyxo-HEXOSE (DAUNOSAMINE) HYDROCHLORIDE FROM D-GLUCOSE

Three different approaches starting from 1,2-O-isopropylidene-α-D-glucofuranose were tested for the synthesis of daunosamine hydrochloride (24), the sugar constituent of the antitumor antibiotics daunomycin and adriamycin.The third route, affording 24 in