35016-92-3

Upstream product

• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 908142-25-6 1-2 O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose 
• 591727-19-4 1-2,5-6 di-O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose 
• 100-44-7 benzyl chloride 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 26928-32-5 3-O-benzyl-5-deoxy-1,2-O-isopropylidene-5-oximino-α-D-xylofuranose 

Downstream Products

• 57973-05-4 (4R)-O³-benzyl-O¹,O²-isopropylidene-4-(5-methyl-isoxazol-3-yl)-β-L-threofuranose 
• 26922-59-8 (4R)-O³-benzyl-O¹,O²-isopropylidene-4-isoxazol-3-yl-β-L-threofuranose 
• 50692-96-1 (4R,4'R)-O³,O^3'-dibenzyl-O¹,O²;O^1',O^2'-diisopropylidene-4,4'-(2-oxy-furazan-3,4-diyl)-bis-β-L-threofuranose 
• 1362080-67-8 C₅₂H₅₇NO₁₀ 
• 1362080-69-0 C₅₂H₅₇NO₁₀ 
• 1362080-52-1 C₅₂H₅₇NO₁₀ 
• 1362080-55-4 C₅₂H₅₇NO₁₀ 
• 1362080-80-5 C₅₂H₅₇NO₁₀ 
• 1362080-82-7 C₅₂H₅₇NO₁₀ 

Relevant academic research and scientific papers

Nitrosocarbonyl Carbohydrate Derivatives: Hetero Diels-Alder and Ene Reaction Products for Useful Organic Synthesis

The generation and trapping of two new nitrosocarbonyl intermediates bearing carbohydrate-based chiral substituents is achieved by the mild oxidation of the corresponding nitrile oxides with tertiary amine N -oxides. Their capture with suitable dienes and alkenes afforded the corresponding hetero Diels-Alder cycloadducts and ene adducts from fair to excellent yields. The entire methodology looks highly promising by the easy conversion of aldoximes into hydroxymoyl halides, widening the access to nitrosocarbonyls, versatile tools in organic synthesis.

Synthesis and biological activities of novel isoxazoline-linked pseudodisaccharide derivatives

A series of novel isoxazoline linked pseudodisaccharide derivatives were regiospecifically synthesized by 1,3-dipolar cycloaddition of α-allyl-C-glycopyranosides and sugar-derived nitrile oxides with good yields. The structures of the compounds were chara