183891-94-3

Upstream product

• 6553-96-4 2,4,6-triisopropylphenylsulfonyl chloride 
• 20439-47-8 (1R,2R)-1,2-diaminocyclohexane 
• 32044-22-7 (1R,2R)-1,2-diaminocyclohexane tartrate 

Downstream Products

• 1155764-04-7 N-((1R,2R)-2-(2,4-diphenyl-1H-pyrrol-1-yl)cyclohexyl)-2,4,6-triisopropylbenzenesulfonamide 
• 6277-67-4 (S)-4-nitro-1,3-diphenylbutan-1-one 
• 1155764-06-9 N-((1R,2R)-2-(4-(4-bromophenyl)-2-phenyl-1H-pyrrol-1-yl)cyclohexyl)-2,4,6-triisopropylbenzenesulfonamide 
• 1268855-66-8 N₁,N₃-bis[(1R,2R)-2-(2,4,6-triisopropylphenylsulfonamido)cyclohexyl]benzene-1,3-disulfonamide 
• 1268855-72-6 N₄,N₄'-bis[(1R,2R)-2-(2,4,6-triisopropylphenylsulfonamido)cyclohexyl]biphenyl-4,4'-disulfonamide 

Relevant academic research and scientific papers

New efficient catalysts for enantioselective transfer hydrogenations

New C2-symmetrical diaminoferrocenyl derivatives 3 and 2-amino(sulfonamido)cyclohexanes 4 were found to be highly active ligands for the ruthenium catalyzed asymmetric transfer hydrogenation of ketones. Contrary to many existing catalytic syste

Cyclohexane-1,2-diamines: Efficient catalysts for the enantioselective conjugate addition of ketones to Nitro Olefins

Simple monosulfonated cyclohexane-1,2-diamines are highly enantioselective organocatalysts for the conjugate addition of ketones to nitro olefins. By focusing on aromatic ketones as the most challenging substrates, selectivities of up to 98 % ee can be ac