168126-70-3

Upstream product

• 177171-55-0 (1S,2R,4R)-7,7-Dimethyl-1-((E)-3-phenyl-allylselanylmethyl)-bicyclo[2.2.1]heptan-2-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 244092-75-9 (1S)-1-phenyl-2-propen-1-amine 
• 100-52-7 benzaldehyde 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 177171-57-2 (1S,3S,5R,7R)-3-Chloro-10,10-dimethyl-3-((E)-3-phenyl-allyl)-4-oxa-3λ⁴-selena-tricyclo[5.2.1.0^1,5]decane 
• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 887113-32-8 4-methyl-N-(2-oxo-1-phenyl-ethyl)-benzenesulfonamide 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 177171-61-8 C₂₆H₃₃NO₃SSe 

Downstream Products

• 887113-26-0 N-allyl-4-methyl-N-(1-phenyl-allyl)-benzenesulfonamide 
• 887113-27-1 (S)-2-phenyl-1-tosyl-2,5-dihydro-1H-pyrrole 
• 887113-28-2 (2R,3R,4S)-2-Phenyl-1-(toluene-4-sulfonyl)-pyrrolidine-3,4-diol 
• 887113-29-3 (3aR,4R,6aS)-2,2-Dimethyl-4-phenyl-5-(toluene-4-sulfonyl)-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole 
• 474558-83-3 (2R,3R,4S)-(-)-N-tert-butoxycarbonyl-3,4-dihydroxy-2-phenyl-pyrrolidine isopropylidene acetal 

Relevant academic research and scientific papers

Direct, enantioselective iridium-catalyzed allylic amination of racemic allylic alcohols

The direct route: Iridium-catalyzed direct conversion of branched allylic alcohols into enantioenriched branched primary allylic amines is highly regio- and enantioselective (see scheme; coe=cyclooctene). Copyright

Asymmetric synthesis of α-amino aldehydes from sulfinimine (N-sulfinyl imine)-derived α-amino 1,3-dithianes. Formal synthesis of (-)-2,3-trans-3,4-cis-dihydroxyproline

Hydrolysis of sulfinimine-derived N-sulfinyl α-amino 1,3-dithianes with aqueous 1,3-dibromo-5,5-dimethylhydantoin affords the corresponding N-tosyl α-amino aldehydes in good yield and high enantiomeric purity. These aldehydes can be reduced to amino alcoh