865253-46-9

Upstream product

• 1354694-95-3 (E)-tert-butyl (3-phenyl-1-(phenylsulfonyl)allyl)carbamate 
• 14371-10-9 (E)-3-phenylpropenal 
• 4248-19-5 tert-butyl carbazate 

Downstream Products

• 1432466-33-5 (E)-ethyl 3-((tert-butoxycarbonyl)amino)-2-diazo-5-phenylpent-4-enoate 
• 1432466-62-0 (2R,3R,E)-ethyl 3-((tert-butoxycarbonyl)amino)-2-hydroxy-5-phenylpent-4-enoate 
• 1432466-48-2 C₁₈H₂₃NO₅ 
• 1373550-35-6 C₂₄H₃₀N₂O₅ 
• 1373550-36-7 C₂₄H₃₀N₂O₅ 
• 1373550-17-4 C₂₄H₂₈N₂O₅ 
• 1373550-16-3 C₂₄H₂₈N₂O₅ 
• 1373550-38-9 benzyl ((1E,3R,4S,5R,6E)-3-(4,5-dibromo-1H-pyrrole-2-carboxamido)-5-hydroxy-1-phenylocta-1,6-dien-4-yl)carbamate 
• 1373550-39-0 benzyl ((1E,3R,4S,5S,6E)-3-(4,5-dibromo-1H-pyrrole-2-carboxamido)-5-hydroxy-1-phenylocta-1,6-dien-4-yl)carbamate 

Relevant academic research and scientific papers

Asymmetric synthesis of anti -β-amino-α-hydroxy esters via dynamic kinetic resolution of β-amino-α-keto esters

A method for the asymmetric synthesis of enantioenriched anti-α-hydroxy-β-amino acid derivatives by enantioconvergent reduction of the corresponding racemic α-keto esters is presented. The requisite α-keto esters are prepared via Mannich addition of ethyl