507454-01-5

Upstream product

• 507453-99-8 anti-(S_S,2S,3S)-(+)-8-chloro-4-[N-(p-toluenesulfinyl)amino]octan-2-ol 
• 507453-97-6 (S_S,3S)-(+)-7-chloro-3-[N-(p-toluenesulfinyl)amino]-N-methoxy-N-methylheptanamide 
• 507453-98-7 (S_S,3S)-(+)-8-chloro-4-[N-(p-toluenesulfinyl)amino]octan-2-one 
• 507453-96-5 (S)-(+)-N-(5-chloropentylidene)-p-toluenesulfinamide 
• 188447-91-8 (S)-p-toluenesulfinimide 
• 20074-80-0 5-chloro-pentanal 

Downstream Products

• 186891-49-6 (+)-(2S)-3-[(2S)-N-(p-toluenesulfonyl)piperidin-2-yl]propan-2-ol 

Relevant academic research and scientific papers

N-sulfinyl beta-amino Weinreb amides: synthesis of enantiopure beta-amino carbonyl compounds. Asymmetric synthesis of (+)-sedridine and (-)-allosedridine.

[reaction: see text] N-Sulfinyl beta-amino Weinreb amides are prepared by condensation of sulfinimines with the potassium enolate of N-methoxy-N-methylacetamide. These new chiral building blocks are useful for the asymmetric synthesis of beta-amino carbon