201354-07-6

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 875-74-1 (R)-phenylglycine 
• 1826-67-1 vinyl magnesium bromide 
• 67341-01-9 (R)-N-(tert-butoxycarbonyl)phenylglycinol 

Downstream Products

• 201354-08-7 (4R,5R)-2,2-Dimethyl-4-phenyl-5-vinyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 201354-11-2 (4R,5S)-5-[(R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-4-phenyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 201354-10-1 (4R,5S)-5-[(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-4-phenyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 201354-09-8 (4R,5S)-5-(1,2-Dihydroxy-ethyl)-2,2-dimethyl-4-phenyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 201354-14-5 Acetic acid (1S,2S)-2,3-diacetoxy-1-((R)-tert-butoxycarbonylamino-phenyl-methyl)-propyl ester 
• 201354-13-4 (4R,5S)-5-((S)-1,2-Diacetoxy-ethyl)-2,2-dimethyl-4-phenyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 201354-12-3 (4R,5S)-5-[2-(tert-Butyl-dimethyl-silanyloxy)-acetyl]-2,2-dimethyl-4-phenyl-oxazolidine-3-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Stereoselective synthesis of polyoxamic acid from (R)-phenylglycine

An efficient route for the synthesis of the biologically important amino acid, polyoxamic acid (1) has been developed via a syn selective Grignard reaction of vinylmagnesium bromide on (R)-N-Boc-phenylglycinal and utilization of the phenyl group as a masked carboxyl synthon.