532989-99-4

Upstream product

• 100-51-6 benzyl alcohol 
• 532989-97-2 (3S,4S)-3-But-3-enyl-1-((R)-1-phenyl-ethyl)-4-((E)-styryl)-azetidin-2-one 
• 127759-27-7 cinnamaldehid-(R)-(+)-α-methylbenzylamine derived imine 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 

Downstream Products

• 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