107575-41-7

Upstream product

• 129966-10-5 (S)-trans-2-phenylcyclohexyl carbamate 
• 34281-92-0 (1S,2R)-trans-2-phenyl-1-cyclohexanol 
• 132746-33-9 carbamic acid (1R,2S)-2-phenylcyclohex-1-yl ester 

Downstream Products

• 132646-22-1 C₂₀H₂₇NO₃S 
• 107575-42-8 N-<carbonyl>-3-but-2-enesulfinamide 
• 129966-09-2 C₁₉H₂₅NO₃S 
• 130061-10-8 C₃₅H₄₇NO₄S 
• 129966-43-4 C₃₅H₄₇NO₄S 
• 129966-17-2 Ethyl-carbamic acid (1R,2S)-2-phenyl-cyclohexyl ester 
• 107575-44-0 N-<carbonyl>-1-cyclopentyl-2-oct-1-enesulfinamide 
• 107575-42-8 N-<carbonyl>-3-but-2-enesulfinamide 
• 107575-47-3 C₂₁H₂₉NO₃S 
• 129966-18-3 N-ethyl-N-<carbonyl>bicyclo<3.3.0>-3-oct-2-enesulfinamide 
• 129966-08-1 C₂₁H₂₉NO₅S 
• 129966-08-1 C₂₁H₂₉NO₅S 
• 107575-45-1 N-<carbonyl>-cis-bicyclo<3.3.0>-3-oct-endo-2-enesulfinamide 
• 107575-43-9 C₂₁H₃₁NO₃S 

Relevant academic research and scientific papers

Asymmetric induction in allylic amination

Net allylic amination of cis-alkenes was accomplished by a two-step procedure that proceeded with excellent regio-and absolute stereochemical control in moderate to good chemical yield. Reaction of alkenes with the N-sulfinylcarbamate of trans-2-phenylcyc

Asymmetric induction in the ene reactions of N-sulfinylcarbamates

Ene reactions of ,N-sulfmylcarbamates derived from the chiral alcohols 8-phenylmenthol and trans-2-phenylcydohexanol proceed with high levels (95+% de) of asymmetric induction. Where regioisomeric products are possible (with unsymmetrical alken