532989-97-2

Upstream product

• 127759-27-7 cinnamaldehid-(R)-(+)-α-methylbenzylamine derived imine 
• 532989-95-0 S-pyridin-2-yl hex-5-enethioate 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 

Downstream Products

• 532989-99-4 (S)-2-[(E)-(S)-3-Phenyl-1-((R)-1-phenyl-ethylamino)-allyl]-hex-5-enoic acid benzyl ester 
• 158414-45-0 (1S,2S)-(+)-2-aminocyclohexane-1-carboxylic acid hydrochloride 
• 532990-01-5 (1S,2S)-2-((R)-1-Phenyl-ethylamino)-cyclohex-3-enecarboxylic acid benzyl ester 

Relevant academic research and scientific papers

A stereoselective synthesis of five- and six-membered cyclic β-amino acids

The cyclic β-amino acids 1 and 2 have been prepared in a short and stereoselective manner. The synthesis features a diastereoselective thioester enolate/imine condensation reaction and a ring-closing metathesis as key processes. Wiley-VCH Verlag GmbH & Co