115522-50-4

Upstream product

• 16801-71-1 N-(4-Oxo-cycloheptyl)-p-toluolsulfonamid 
• 5452-35-7 cycloheptanamine 
• 80-30-8 N-cyclohexyl-p-toluenesulfonamide 
• 97399-15-0 Acetic acid (1S,4R)-4-(toluene-4-sulfonylamino)-cyclohept-2-enyl ester 
• 82736-40-1 (Z)-1-acetoxy-4-chlorocyclohept-2-ene 
• 876938-53-3 Cyclohepta-1,3-diene 
• 115522-48-0 Acetic acid (1S,4R)-4-(toluene-4-sulfonylamino)-cycloheptyl ester 
• 97399-15-0 Acetic acid (1R,4R)-4-(toluene-4-sulfonylamino)-cyclohept-2-enyl ester 
• 115522-48-0 Acetic acid (1R,4R)-4-(toluene-4-sulfonylamino)-cycloheptyl ester 
• 16801-64-2 4-methyl-N-(4-oxo-cyclohexyl)benzenesulfonamide 
• 16801-70-0 N-cycloheptyl-4-methylbenzenesulfonamide 

Downstream Products

• 95687-91-5 N-(4-Hydroxy-cycloheptyl)-benzamid 
• 115522-40-2 (1R,5S)-8-tosyl-8-azabicyclo[3.2.1]octane 
• 115522-56-0 N-((1R,4R)-4-Chloro-cycloheptyl)-4-methyl-benzenesulfonamide 
• 115522-54-8 Methanesulfonic acid (1R,4R)-4-(toluene-4-sulfonylamino)-cycloheptyl ester 
• 14156-24-2 N-(4-Oxo-cycloheptyl)-benzamide 

Relevant academic research and scientific papers

STEREOCONTROLLED SYNTHESIS OF TROPANOL DERIVATIVES VIA PALLADIUM-CATALYZED REACTIONS

A general method for the transformation of 1,3-cycloheptadienes to tropane alkaloid derivatives was developed.The procedure was applied to the stereocontrolled synthesis of the exo- and endo-tropanol derivatives 1 and 2.The approach is based on a dual stereocontrol in the 1,4-functionalization of conjugated dienes.