36617-87-5

Upstream product

• 36617-84-2 (R/S)-N,N-dimethyl-(3-phenylbutyl)amine 
• 5801-17-2 1-bromo-3-phenylbutane 
• 86437-06-1 (S)-(+)-N,N-dimethyl-3-phenylbutanamine 
• 4593-90-2 (S)-2-phenylbutanoic acid 
• 68679-84-5 (S)-3-phenyl butyric acid chloride 
• 86437-05-0 (S)-N,N-dimethyl-3-phenylbutyramide 

Downstream Products

• 934-10-1 3-phenylbut-1-ene 
• 86437-07-2 (-)-N,4-dimethyl-N-<<(E)-3-phenyl-2-butenyl>sulfinyl>-benzenesulfonamide 
• 81654-84-4 (-)-4-methyl-N-<<(E)-3-phenyl-2-butenyl>sulfinyl>-benzenesulfonamide 
• 58717-85-4 (S)-3-phenyl-1-butene 

Relevant academic research and scientific papers

Ene Reaction Mechanisms. 1. Chirality Transfer to the Enophile 4-Methyl-N-sulfinylbenzenesulfonamide

The ene reaction of (S)-(+)-3-phenyl-1-butene (1) with N-sulfinyl-p-toluenesulfonamide (2) leads to the optically active (E)-2-alkenesulfinamide 3.This corresponds to a chirality transfer from the chiral carbon center in 1 to the sulfur atom of the produc