174787-58-7

Upstream product

• 100-58-3 phenylmagnesium bromide 
• 124-63-0 methanesulfonyl chloride 
• 174787-57-6 (4S,5S)-5-(2-hydroxy)ethyl-4-phenyl-2-oxazolidinone 

Downstream Products

• 174787-59-8 (4S,5S)-5-(2-phenylselenenyl)ethyl-4-phenyl-2-oxazolidinone 
• 143615-03-6 (4S,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid 

Relevant academic research and scientific papers

Synthetic application of chiral 4-methoxy-2-oxazolidinone synthons to 2-amino alcohols of biological interest

The versatility as chiral synthons of (4S, 5S)- and (4R, 5R)-5-allyl-4-methoxy-2-oxazolidinones, readily obtainable from 3-[(1S)-2-exo-alkoxy-1-apocamphanecarbonyl]-2-oxazolone, is demonstrated by the facile stereospecific conversions to (2R, 3S)-3-amino-2-hydroxy-3-phenylpentanoic acid, (2R, 3R, 5E, 7E)-2-amino-5,7-tetradecadien-3-ol and (2S, 3R)-dihydrosphingosine.