117499-04-4

Upstream product

• 143-33-9 sodium cyanide 
• 98105-42-1 (S)-2-(t-butoxycarbonylamino)-3-cyclohexyl-1-propanal 
• 151-50-8 potassium cyanide 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 103322-56-1 tert-butyl [(1S)-2-cyclohexyl-1-(hydroxymethyl)ethyl]carbamate 
• 115766-13-7 (S)-α-[[(1,1-dimethylethoxy)carbonyl]amino]-N-methoxy-N-methylcyclohexanepropanamide 
• 37736-82-6 (S)-2-tert-butoxycarbonylamino-3-cyclohexylpropionic acid 
• 117499-02-2 ((S)-2-Cyano-1-cyclohexylmethyl-2-trimethylsilanyloxy-ethyl)-carbamic acid tert-butyl ester 

Downstream Products

• 167823-30-5 ((1S,2R)-1-Cyclohexylmethyl-2-hydroxy-5-methyl-3-oxo-hexyl)-carbamic acid ethyl ester 
• 167823-29-2 4-cyclohexyl-3-(S)-ethoxycarbonylamino-2-(R)-hydroxybutyric acid 
• 156540-64-6 ((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-methyl-hexyl)-carbamic acid ethyl ester 
• 122621-77-6 (2S,3R,4S)-2-amino-1-cyclohexyl-3,4-dihydroxy-6-methylheptane 
• 121506-22-7 (2R,3S)-nor-C-statine hydrochloride 

Relevant academic research and scientific papers

Unique Stereocontrol in Europium (III)-Catalyzed Cyanosilylation of chiral α-Alkoxy and α-Amino Aldehydes

The Eu(III)-catalyzed cyanosilylations of chiral α-alkoxy and α-amino aldehydes are shown to exhibit syn diastereofacial selection, the degree increasing with an increase in steric bulk of the alkyl chain in the aldehydes.The mechanism of this catalytic p