77803-79-3

Upstream product

• 56239-25-9 (+/-)-2-Oxa-3-azabicyclo[2.2.2]oct-5-ene hydrochloride 
• 108-24-7 acetic anhydride 
• 77803-77-1 (1S*,4R*)-4-aminocyclohex-2-enol 

Downstream Products

• 77803-82-8 c-2-Acetoxy-t-3-brom-c-4-hydroxy-r-1-cyclohexylammoniumbromid 
• 77803-83-9 N-(t-3-Brom-c-2,c-4-dihydroxy-r-1-cyclohexyl)acetamid 

Relevant academic research and scientific papers

Polyhydroxyamino Compounds via Diene Synthesis with Nitroso Compounds, IV. - Preparation and Stereochemistry of Dideoxyinosamine Derivatives

The general method for the synthesis of polyhydroxy amines by Diels-Alder reactions with a nitroso compound, reduction of the adduct with cleavage of the N - O bond and hydroxylation of the remaining C = C -double bond, can also be realized with α-chloronitrosocyclohexane as dienophile, in good yield.Primary amines are synthesized in this way.