82985-18-0

Upstream product

• 70853-26-8 N-carbobenzoxy-L-leucinal 
• 118247-68-0 N-Benzyloxycarbonyl-L-Homoleucine 
• 937793-04-9 (4S,5S)-N-benzyloxycarbonyl-5-hydroxy-4-isobutyl-1,3-oxazinan-6-one 
• 922705-34-8 phenylmethyl (4S)-4-(2-methylpropyl)-6-oxo-1,3-oxazinane-3-carboxylate 
• 126535-80-6 (2S,3S)-3-Benzyloxycarbonylamino-2-hydroxy-5-methyl-hexanoic acid methyl ester 

Relevant academic research and scientific papers

Diastereoselective synthesis of α-methyl and α-hydroxy-β- amino acids via 4-substituted-1,3-oxazinan-6-ones

(Chemical Equation Presented) 1,3-Oxazinan-6-ones have been utilized in a series of enolate reactions to produce 5-hydroxy and 5-alkyl-4-substituted-1,3- oxazinan-6-ones with excellent trans diastereoselectivity. Highlighting the versatility of the oxazin

Tributyltin Cyanide, a Novel Reagent for the Stereoselective Preparation of 3-Amino-2-hydroxy Acids via Cyanohydrin Intermediates

Reaction of tributyltin cyanide with optically active 2-N-benzyloxycarbonylamino aldehydes 1 gives the corresponding O-tributylstannyl cyanohydrins 2 and 3 stereoselectively.Compounds 2 and 3 are transformed in situ into the methyl 3-N-benzyloxycarbonylam