84730-17-6

Upstream product

• 100-52-7 benzaldehyde 
• 84730-20-1 3,6-epimino-3,6-dideoxy-1,2-O-isopropylidene-α-D-glucofuranose 
• 22169-72-8 3-azido-3-deoxy-6-O-toluene-p-sulphonyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 22169-71-7 (R)-1-((3aR,5S,6S,6aR)-6-azido-2,2-dimethyltetrahydrofuro-[2,3-d][1,3]dioxol-5-yl)ethane-1,2-diol 
• 16848-19-4 3-amino-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 93-97-0 benzoic acid anhydride 
• 84730-09-6 3-benzylidenimido-3-deoxy-1,2;5,6-di-O-isopropylidene-α-D-glucofuranose 
• 81645-62-7 3-Benzamido-3-desoxy-1,2;5,6-di-O-isopropyliden-α-D-glucofuranose 

Downstream Products

• 960324-94-1 C₁₆H₂₀FNO₃ 
• 960324-93-0 C₁₃H₁₆FNO₂ 
• 960324-95-2 C₁₇H₂₀FNO₅ 

Relevant academic research and scientific papers

BICYCLIC COMPOUNDS USEFUL AS CATHEPSIN S INBHIBITORS

Compounds of formula (I), wherein R1, R2, R3, Ra and E are are defined within, and pharmaceutically acceptable salts, solvates, hydrates and N-oxides thereof having utility in the treatment of disorders mediated by cathepsin S.

REDUCTION OF 1,2;5,6-DI-O-ISOPROPYLIDENE-α-D-GLUCOFURANOSE DERIVATIVES WITH LITHIUM ALUMINIUM HYDRIDE; A FACILE SYNTHETIC METHOD FOR 3,6-IMINO DERIVATIVES

Treatment of 3-acylamido- or alkylimino-3-deoxy-1,2;5,6-di-O-isopropylidene-α-D-glucofuranose with lithium aluminium hydride in boiling 1,4-dioxane afforded unusual products, namely, 3,6-N-alkylimino-3,6-dideoxy-1,2-O-isopropylidene-α-D-glucofuranose or 6