936112-24-2

Upstream product

• 936112-20-8 1-C-allyl 2,3-di-O-benzyl-6-C-nitro-6-deoxy-α-D-ribo-hexano-furanoside 
• 842130-93-2 ((2R,3R,4S,5R)-5-Allyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yl)-methanol 
• 936112-16-2 1-C-allyl 2,3-di-O-benzyl-5-aldo-α-D-ribofuranoside 
• 936112-17-3 1-(5-allyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yl)-2-nitro-ethanol 
• 936112-19-5 1-C-allyl 2,3-di-O-benzyl-6-C-nitro-6-deoxy-α-D-ribo-hex-5-eno-furanoside 

Downstream Products

• 936112-38-8 (1S,2S,3R,4R,6R)-2,3-di-O-benzyl-1-formylmethyl-4-hydroxy-6-nitrocyclohexane 
• 936112-36-6 (1S,2S,3R,4R,6S)-2,3-di-O-benzyl-1-formylmethyl-4-hydroxy-6-nitrocyclohexane 
• 936112-44-6 (1S,2S,3R,4R,6S)-1-methoxycarbonylmethyl-2,3-di-O-benzyl-4-hydroxy-6-nitrocyclohexane 
• 936112-26-4 methyl 2-C-(2,3-di-O-benzyl-6-C-nitro-6-deoxy-α-D-ribo-hexano-furanosyl)acetate 

Relevant academic research and scientific papers

Polyhydroxylated indolines and oxindoles from C-glycosides via sequential Henry reaction, Michael addition, and reductive amination/amidation

6-Nitro-2′-carbonyl-C-glycofuranosides synthesized via Henry reaction from 1-C-allyl 5-aldo-C-glycoside underwent an intramolecular Michael addition to afford nitrocyclohexanol derivatives in good to excellent yield. Reduction of the nitro group followed