6752-49-4

Upstream product

• 16718-95-9 methyl 4,6-O-benzylidene-2-deoxy-α-D-altropyranoside 
• 4234-42-8 methyl 4,6-O-benzylidene-2-O-p-toluenesulphonyl-α-D-ribohexopyranosid-3-ulose 
• 96779-98-5 methyl 3-O-acetyl-4,6-O-benzylidene-2-O-(trifluoromethanesulfonyl)-α-D-mannopyranoside 
• 6698-32-4 methyl 4,6-O-benzylidene-2-O-toluene-p-sulfonyl-α-D-glucopyranoside 
• 2872-56-2 methyl 3-O-acetyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 3150-15-0 methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside 

Downstream Products

• 63554-26-7 (5R)-2t-phenyl-4t-(1⁽²⁾H-pyrazol-3-yl)-[1,3]dioxan-5r-ol 
• 120401-20-9 methyl 4,6-O-benzylidene-2-deoxy-3-C-vinyl-α-D-ribo-hexopyranoside 
• 85632-67-3 (4aR,6S,8S,8aR)-6-Methoxy-8-nonyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-ol 
• 79621-95-7 (4aR,6S,8aS)-8-[1-Butoxy-meth-(E)-ylidene]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 66101-30-2 methyl 4,6-O-benzylidene-2-deoxy-β-D-erythro-hexopyranosid-3-ulose 
• 130781-44-1 methyl 4-O-benzoyl-6-bromo-2,6-dideoxy-α-D-erythro-hexopyranosid-3-ulose 
• 79646-67-6 [(4aR,6S,8aS)-6-Methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-(8E)-ylidene]-acetic acid methyl ester 
• 6752-52-9 Methyl-4,6-O-benzyliden-2-desoxy-3-C-methyl-α-D-ribo-hexopyranosid 
• 13264-05-6 methyl 3,3'-anhydro-4,6-O-benzylidene-2-deoxy-3-C-hydroxymethyl-α-D-arabino-hexopyranoside 
• 13264-05-6 methyl 3,3'-anhydro-4,6-O-benzylidene-2-deoxy-3-C-hydroxymethyl-α-D-ribo-hexopyranoside 
• 63803-49-6 methyl 4,6-O-benzylidene-2,3-dideoxy-3-C-methylene-α-D-erythro-hexopyranoside 
• 79607-56-0 Methyl 4,6-O-benzylidene-2-deoxy-3-C-formyl-α-D-arabino-hexopyranoside 
• 120016-85-5 Methyl 3-azido-4,6-O-benzylidene-2,3-dideoxy-3-C-formyl-α-D-arabino-hexopyranoside 
• 120016-87-7 ((4aR,6S,8S,8aS)-8-Azido-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-methanol 

Relevant academic research and scientific papers

MODIFIED PYRIDINIUM DICHROMATE OXIDATION. A FACILE SYNTHESIS OF THE KEY 3-KETO SUGAR INTERMEDIATE FOR L-DAUNOSAMINE

An efficient procedure is described for the large scale prepration of the key 3-keto sugar intermediate in the synthesis of L-daunosamine, using readily available and relatively inexpensive chemicals, under mild conditions.A simple and effective work up,

A Convenient Synthesis of Methyl 4,6-O-Benzylidene-2-deoxy-α-D-erythro-hexopyranosid-3-ulose

Methyl 4,6-O-benzylidene-2-deoxy-α-D-erythro-hexopyranosid-3-ulose, a key intermediate in the synthesis of L-daunosamine, has been prepared in 100 g lots starting from D-glucose.

An investigation of the Kishner elimination as a route to dideoxy sugars

Methyl 4,6-O-benzylidene-2-O-p-toluenesulphonyl-α-D-ribohexopyranosid-3-ulose has been used as a substrate for an investigation of the Kishner elimination as a route to deoxygenated sugars.The conditions of the reaction of the ketotosylate with hydrazine