163299-89-6

Upstream product

• 4277-63-8 methyl 1H-pyrrole-1-carboxylate 
• 5324-64-1 2-(benzenesulfonyl)ethynylbenzene 

Downstream Products

• 1099378-31-0 2-phenyl-7-aza-bicyclo [2.2.1]heptane 
• 1099378-32-1 2-phenyl-7-aza-bicyclo[2.2.1]hept-5-ene 

Relevant academic research and scientific papers

A VERSATILE TOTAL SYNTHESIS OF EPIBATIDINE AND ANALOGS

A racemic mixture of epibatidine, a potent analgesic alkaloid possessing a 7-azanorbornane structure, has been synthesized via a versatile four-step synthetic route: a Diels-Alder reaction of N-carbomethoxy pyrrole and phenylsulfonyl 6-chloro-3-pyridyl ac

7-azabicyclo[2.2.1]-heptane and -heptene derivatives as cholinergic receptor ligands

7-Azabicyclo[2.2.1]-heptane and -heptene derivatives are disclosed that can be administered to a mammal, including a human, to treat disorders associated with a decrease or increase in cholinergic activity.