96303-87-6

Upstream product

• 21286-54-4 Camphorsulfonyl chloride 
• 101-83-7 N-cyclohexyl-cyclohexanamine 
• 141847-68-9 C-((1R,2R,4R)-2-Chloro-7,7-dimethyl-2-nitroso-bicyclo[2.2.1]hept-1-yl)-N,N-dicyclohexyl-methanesulfonamide 
• 21286-54-4 (+)-(1S)-Campher-10-sulfonsaeure-chlorid 
• 141847-70-3 C₂₉H₅₀N₂O₄S 
• 141847-71-4 C₂₈H₄₈N₂O₄S 
• 141847-72-5 C₂₇H₄₆N₂O₄S 

Downstream Products

• 150763-96-5 (-)-10-<(N,N-Dicyclohexylamino)sulfonyl>camphor N-(benzylsulfonyl)imine 
• 96303-88-7 (-)-10-dicyclohexylsulfamoyl-D-isoborneol 
• 141847-68-9 C-((1R,2R,4R)-2-Chloro-7,7-dimethyl-2-nitroso-bicyclo[2.2.1]hept-1-yl)-N,N-dicyclohexyl-methanesulfonamide 
• 324016-34-4 N,N-dicyclohexyl-C-(7,7-dimethyl-2-thioxo-bicyclo[2.2.1]hept-1-yl)-methanesulfonamide 
• 324016-35-5 N,N-dicyclohexyl-C-(2-mercapto-7,7-dimethyl-bicyclo[2.2.1]hept-1-yl)-methanesulfonamide 
• 324016-36-6 Thioacetic acid S-{(1R,2R,4R)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl} ester 
• 324016-37-7 N,N-dicyclohexyl-C-[7,7-dimethyl-2-(1-trimethylsilanyloxy-vinylsulfanyl)-bicyclo[2.2.1]hept-1-yl]-methanesulfonamide 
• 324016-38-8 C-{2-[1-(tert-butyl-dimethyl-silanyloxy)-vinylsulfanyl]-7,7-dimethyl-bicyclo[2.2.1]hept-1-yl}-N,N-dicyclohexyl-methanesulfonamide 
• 324016-39-9 N,N-dicyclohexyl-C-[7,7-dimethyl-2-(1-triisopropylsilanyloxy-vinylsulfanyl)-bicyclo[2.2.1]hept-1-yl]-methanesulfonamide 
• 141847-69-0 C₃₁H₄₆N₂O₄S 
• 141847-72-5 C₂₇H₄₆N₂O₄S 
• 141847-72-5 C₂₇H₄₆N₂O₄S 
• 141847-70-3 C₂₉H₅₀N₂O₄S 
• 141847-70-3 C₂₉H₅₀N₂O₄S 

Relevant academic research and scientific papers

Application in asymmetric Morita-Baylis-Hillman reactions

N-Substituted 2-exo-hydroxybornyl-10-sulfonamides, prepared as potential chiral auxiliaries for use in asymmetric Morita-Baylis-Hillman (MBH) reactions, have been treated with acryloyl chloride to afford the corresponding 2-exo-Acrylate esters as MBH subs

ASYMMETRIC DIELS-ALDER REACTIONS: FACILE PREPARATION AND STRUCTURE OF SULFONAMIDO-ISOBORNYL ACRYLATES

The crystalline chiral auxiliaries 2, 3 and 4 were prepared from champhor-10-sulfonyl chlorides in 2 steps.Their readily accessible acrylates underwent efficient asymmetric Diels-Alder additions to cyclopentadiene, the topicity of wich agrees with X-ray evidence.