191721-06-9

Upstream product

• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 191721-03-6 (Z)-N-benzyl-(3-O-benzyl-1,2-O-isopropylidene-5-deoxy-α-D-ribofuranos-5-ylidene)amine N-oxide 
• 162740-21-8 (Z)-N-benzyl-(3-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranos-5-ylidene)amine N-oxide 
• 29601-98-7 N-benzylhydroxylamine hydrochloride 
• 63593-02-2 3-O-benzyl-1,2-O-isopropylidene-α-D-ribo-pentodialdo-1,4-furanose 
• 100-46-9 benzylamine 
• 41341-67-7 3-O-Benzyl-6-desoxy-1,2-O-isopropyliden-5-O-(p-tolylsulfonyl)-α-D-gluco-hexofuranose 
• 868078-75-5 3-O-benzyl-5-benzylamino-5,6-dideoxy-1,2-O-isopropylidene-(6-C-p-tolylsulfonyl)-β-L-ido-1,4-furanose 
• 100-39-0 benzyl bromide 
• 191721-01-4 N-Benzyl-N-[(S)-1-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl]-hydroxylamine 

Relevant academic research and scientific papers

A diastereoselective and general route to 5-amino-5-deoxysugars: Influence of C-3 substitution on the addition of amines to C-5 of vinyl sulfone-modified Hex-5-enofuranosyl carbohydrates

In the synthesis of vinyl sulfone-modified hex-5-enofuranosides, the E/Z ratios of the products are influenced by the stereoelectronic property of a group present at the C-3 position. This observation has been utilized to influence the diastereoselectivit

A new route to aminosugars from sugar nitrones: Synthesis of 6-deoxynojirimycin

The 1,3-addition of methylmagnesium chloride to dialdose derived nitrones 3 and 7 afforded N-benzylhydroxylamines 4/5 and 8/9, respectively, in high yields. The stereoselectivity of the addition was improved by the use of trimethylsilyl triflate. The N-O