113283-75-3

Upstream product

• 59830-60-3 benzyl (1S)-(1-formyl-2-phenylethyl)carbamate 
• 72345-23-4 (2S,4S)-pentane-2,4-diol 
• 59830-61-4 (S)-(1-benzyl-2,2-dimethoxyethyl)carbamic acid benzyl ester 
• 6372-14-1 N-((benzyloxy)carbonyl)-L-phenylalaninol 

Downstream Products

• 113350-25-7 [(1S,2S)-1-Benzyl-2-((1S,3S)-3-hydroxy-1-methyl-butoxy)-pent-4-enyl]-carbamic acid benzyl ester 
• 113283-81-1 [(1S,2R)-1-Benzyl-2-((1S,3S)-3-hydroxy-1-methyl-butoxy)-pent-4-enyl]-carbamic acid benzyl ester 
• 62023-60-3 (2R,3S)-N-(benzyloxycarbonyl)-3-amino-2-hydroxy-4-phenylbutanoic acid 
• 62023-59-0 (2S,3S)-3-benzyloxycarbonylamino-2-hydroxy-4-phenylbutanoic acid 
• 126015-23-4 (2S,3S)-3-[[(benzyloxy)carbonyl]amino]-2-hydroxy-4-phenylbutanoic acid methyl ester 
• 126015-22-3 (2R,3S)-3-[[(benzyloxy)carbonyl]amino]-2-hydroxy-4-phenylbutanoic acid methyl ester 
• 113283-84-4 (4S,5R)-4-benzyl-5(1-propenyl)-1,3-oxazolidin-2-one 

Relevant academic research and scientific papers

Stereoselection in the Synthesis of threo- and erythro-3-Amino-2-hydroxy-4-phenyl-butanoic Acid using Chiral Acetal Templates

Boron trifluoride-diethyl ether mediated addition of trimethylsilylcyanide (TMSCN) to the chiral acetals derived from Z-L- and Z-D-phenyl alaninal, Z-N-benzyloxycarbonyl), and (+)-(2S,4S)- and (-)-(2R,4R)-2,4-pentanediol stereoselectivity gave the four st

Asymmetric Synthesis of 2- Amino Alcohol Derivatives from (S)-α-Amino Aldehydes via Acetal Templates

Titanium tetrachloride mediated addition of allyltrimethylsilane to chiral acetals derived from (S)-α-amino aldehydes and (+)-(2S,4S)-pentane-2,4-diol gave the anti-2-amino alcohol derivatives with considerably high diastereoselectivity.On the other hand,