229981-17-3

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 124915-64-6 (4S,5R)-5-ethenyl-4-phenylmethyloxazolidin-2-one 
• 265996-19-8 (4S,5RS)-5-ethenyl-4-phenylmethyloxazolidin-2-one 
• 99113-30-1 ((1S,2R)-1-benzyl-2-hydroxybut-3-enyl)carbamic acid tert-butyl ester 

Downstream Products

• 229981-31-1 (3R,4S)-N-(tert-butoxycarbonyl)-4-amino-3-(tert-butyldimethylsilyloxy)-1-hydroxy-5-phenylpentane 
• 229981-33-3 tert-butyl (2S,3R)-2-benzyl-3--5-oxo-1-pyrrolidinecarboxylate 
• 229981-28-6 (3R,4S)-N-(tert-butoxycarbonyl)-4-amino-3-(tert-butyldimethylsilyloxy)-5-phenylpent-1-ene 
• 229981-04-8 (3R,4S)-4--3-(methoxymethoxy)-5-phenylpentanoic acid 
• 229981-25-3 (3R,4S)-4--3-(methoxymethoxy)-1-hydroxy-5-phenylpentane 
• 229981-21-9 (3R,4S)-N-(tert-butoxycarbonyl)-4-amino-3-(methoxymethoxy)-5-phenylpent-1-ene 
• 229981-23-1 (3R,4S)-4--3-(methoxymethoxy)-5-phenylpent-1-ene 
• 482374-29-8 4-benzyl-5-(2-tert-butoxycarbonyl-vinyl)-2-oxo-oxazolidine-3-carboxylic acid tert-butyl ester 
• 99113-30-1 ((1S,2R)-1-benzyl-2-hydroxybut-3-enyl)carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Regio- and stereoselective ring-opening of chiral 1,3-oxazolidin-2-one derivatives by organocopper reagents provides novel access to di-, tri- and tetra-substituted alkene dipeptide isosteres

Organocopper-mediated alkylation of β-(N-Boc-2-oxo-1,3-oxazolidin-5-yl)-α,β-enoates has been intensively investigated. Alkylation proceeded regio- and stereoselectively by anti-SN2′ ring-opening to provide a new route to the synthesis of Ψ[(E)-