1240292-75-4

Upstream product

• 1213834-90-2 C₁₀H₁₃NO 
• 98-88-4 benzoyl chloride 
• 58824-49-0 1-(2-methoxyphenyl)prop-2-en-1-ol 
• 1240292-71-0 (S)-1-(2-methoxyphenyl)prop-2-en-1-ol 

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

Stereospecific substitution of allylic alcohols to give optically active primary allylic amines: Unique reactivity of a (P,alkene)Ir complex modulated by iodide

A stereospecific allylic amination of unactivated secondary (2°)-allylic alcohols is reported. The primary (1°)-allylic amine can be isolated directly or protected in situ. Spectroscopic studies have shed light on the structure of the catalytically active Ir?(P,olefin)2I complex.