130203-12-2

Upstream product

• 60261-46-3 (2S)-2-[(diphenylphosphino)methyl]pyrrolidine 
• 108-94-1 cyclohexanone 
• 86661-32-7 (S)-tert-butyl 2-((tosyloxy)methyl)pyrrolidine-1-carboxylate 
• 135055-75-3 (S)-(-)-N-tert-butoxycarbonyl-2-<(diphenylphosphino)methyl>pyrrolidine 
• 135097-23-3 (2S)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester 
• 69610-40-8 N-(tert-butoxycarbonyl)-L-prolinol 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 

Downstream Products

• 36302-35-9 (S)-2-allylcyclohexanone 
• 94-66-6 (R)-2-allylcyclohexanone 

Relevant academic research and scientific papers

Palladium-catalyzed asymmetric allylations of chiral enamines bearing phosphine functionality. Effects of anionic counterparts of allylating reagents on asymmetric induction

Palladium-catalyzed asymmetric allylations of chiral enamines bearing a phosphine group were attempted using various allylating reagents to produce optically active α-allyl carbonyl compounds. The great effects of the anionic counterparts of the allylatin