894423-96-2

Upstream product

• 69048-60-8 meso-(1R,3S,4S,6R)-4,6-diazidocyclohexane-1,3-diol 
• 285-52-9 cis-4,8-dioxa-tricyclo[5.1.0.0^3,5]octane 
• 108-05-4 vinyl acetate 
• 53534-92-2 (1R,2R,4S,5S)-6,7-diazabicyclo[3.2.1]octane-2,4-diol 
• 55659-50-2 2,5-dideoxystreptamine 
• 73023-64-0 (1R,3S,4S,6R)-4,6-bis(benzylamino)cyclohexane-1,3-diol dihydrochloride 

Downstream Products

• 1223053-77-7 (1R,2R,4S,5S)-2,4-diazido-5-(methoxymethoxy)cyclo-hexyl acetate 
• 1223054-06-5 C₁₆H₂₀N₆O₄ 

Relevant academic research and scientific papers

Enzymatic desymmetrization of 2,5-dideoxystreptamine precursors

The stereoselective enzymatic acylation of meso-6,7-diazabicyclo[3.2.1]oct-6-ene-2,4-diol 4 and meso-4,6-diazidocyclohexane-1,3-diol 5 in organic media gave the corresponding monoesters in high enantiomeric excess. The hydrolysis of the corresponding diac

The chemistry of amine-azide interconversion: Catalytic diazotransfer and regioselective azide reduction

Azides have proven to be useful precursors to amines in organic syntheses. This report describes an improvement of the diazotransfer reaction and the first example of a regioselective azide reduction of compounds containing multiple azides. The use of a s