130695-52-2

Upstream product

• 20053-48-9 L-bornyl p-toluenesulfonate 
• 17356-08-0 thiourea 

Downstream Products

• 1416720-84-7 (1S,2S,4S,E)-N-(2-hydroxy-5-chlorobenzylidene)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-sulfenamide 
• 1416720-85-8 (1S,2S,4S,E)-N-(2-hydroxy-5-bromobenzylidene)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-sulfenamide 
• 1416720-86-9 (1S,2S,4S,E)-N-(4-nitrobenzylidene)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-sulfenamide 
• 1416720-87-0 (1S,2S,4S,E)-N-(4-dimethylaminobenzylidene)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-sulfenamide 
• 1416721-04-4 (R,1S,2S,4S,E)-N-(4-nitrobenzylidene)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-sulfinamide 
• 1416721-05-5 (S,1S,2S,4S,E)-N-(4-nitrobenzylidene)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-sulfinamide 
• 1416720-80-3 (1S,2S,4S,E)-N-(2-hydroxybenzylidene)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-sulfenamide 
• 1416720-89-2 (R)-N-(E)-(2-hydroxybenzylidene)-{(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane}-2-sulfinamide 
• 1416720-88-1 (S)-N-(E)-(2-hydroxybenzylidene)-{(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane}-2-sulfinamide 
• 1416720-91-6 (R)-N-(E)-(2-hydroxy-3,5-dibromobenzylidene){(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]-heptane}-2-sulfinamide 
• 1416720-90-5 (S)-N-(E)-(2-hydroxy-3,5-dibromobenzylidene){(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]-heptane}-2-sulfinamide 
• 1416720-93-8 (R)-N-(E)-(2-hydroxy-3,5-diiodobenzylidene)-{(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane}-2-sulfi namide 
• 1416720-92-7 (S)-N-(E)-(2-hydroxy-3,5-diiodobenzylidene)-{(1S,2S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane}-2-sulfi namide 
• 1416720-96-1 (R)-N-(E)-(2-hydroxy-3,5-di-tert-butylbenzylid-ene)-{(1S,2S,4S)-1,7,7-trimethylbicyclo-[2.2.1]heptane}-2-sulfinamide 

Relevant academic research and scientific papers

Synthesis and reduction of new sulfinimines with isobornane structure

Synthesis of sulfenimines proceeding from isobornanethiol with yields up to 78% was performed. They were oxidized to diastereomeric isobornylsulfinimines and the latter were reduced to N-substituted isobornylsulfinamides in high yields.