176791-36-9

Upstream product

• 176649-80-2 N-<2-(2-Hydroxyethyl)cyclohex-2-enyl>-N-(2-nitrophenyl)methanesulfonamide 
• 176649-71-1 N-(2-Nitrophenyl)-N-(2-prop-2-enylcyclohex-2-enyl)methanesulfonamide 
• 176649-74-4 N-<2-(2,3-Dihydroxypropyl)cyclohex-2-enyl>-N-(2-nitrophenyl)methanesulfonamide 
• 176649-77-7 N-(2-Nitrophenyl)-N-<2-(2-oxoethyl)cyclohex-2-enyl>methanesulfonamide 
• 176649-68-6 2-(prop-2'-enyl)-cyclohex-2-en-1-ol 
• 88-74-4 2-nitro-aniline 
• 38019-50-0 2-allyl-cyclohex-2-enone 
• 176791-35-8 N-<2-(2-Methylsulfonyloxyethyl)cyclohex-2-enyl>-N-(2-nitrophenyl)methanesulfonamide 
• 85150-03-4 N-(2-nitrophenyl)methanesulfonamide 

Downstream Products

• 176791-28-9 N-(2-Aminophenyl)-N-<2-<2-(trifluoroacetamido)ethyl>cyclohex-2-enyl>methanesulfonamide 
• 176791-38-1 N-(2-Nitrophenyl)-N-<2-<2-(trifluoroacetamido)ethyl>cyclohex-2-enyl>methanesulfonamide 
• 176791-37-0 N-[2-(2-Amino-ethyl)-cyclohex-2-enyl]-N-(2-nitro-phenyl)-methanesulfonamide 

Relevant academic research and scientific papers

Tetrathiafulvalene-mediated stereoselective synthesis of the tetracyclic core of Aspidosperma alkaloids

A novel route to advanced synthetic precursors of Aspidosperma alkaloids is described, utilising radical-polar crossover reactions.

Studies of the tetrathiafulvalene mediated radical-polar crossover reaction directed toward the total synthesis of alkaloid natural products

The carbon skeleton of octahydro-1H-pyrrolo[2,3-d]carbazole (4), a tetracylic sub-unit which is common to a wide range of alkaloid natural products has been prepared by two approaches which exploit the one-pot radical-polar crossover chemistry mediated by