220931-41-9

Upstream product

• 1161-13-3 N-Cbz-L-Phe 
• 55740-07-3 (4S)-4-benzyl-5-oxo-1,3-oxazolidine-3-carboxylic acid benzyl ester 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 

Downstream Products

• 178113-66-1 (3R,4S)-4-(tert-Butoxycarbonyl-methyl-amino)-3-(tert-butyl-dimethyl-silanyloxy)-5-phenyl-pentanoic acid 
• 223908-36-9 4-(tert-butoxycarbonyl-methyl-amino)-3-(tert-butyl-dimethyl-silanyloxy)-5-phenyl-pentanoic acid ethyl ester 
• 223908-35-8 (3R,4S)-4-(Benzyloxycarbonyl-methyl-amino)-3-(tert-butyl-dimethyl-silanyloxy)-5-phenyl-pentanoic acid ethyl ester 
• 182567-73-3 (4S,5S)-1-benzyloxycarbonyl-5-benzyl-4-hydroxy-2-oxopyrrolidine 
• 129029-32-9 (4S,5S)-5-Benzyl-2-oxo-4-hydroxypyrrolidine 
• 109579-10-4 (4S,5R)-N-(((tert)-butyloxy)carbonyl)-5-benzyl-4-hydroxy-2-pyrrolidinone 
• 72155-48-7 (3S,4S)-4-tert-butoxycarbonylamino-3-hydroxy-5-phenylpentanoic acid 
• 236747-30-1 4-(tert-butoxycarbonyl-methyl-amino)-3-oxo-5-phenyl-pentanoic acid ethyl ester 
• 936226-69-6 (3R,4S)-4-tert-Butoxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-5-phenyl-pentanoic acid ethyl ester 
• 178267-25-9 (3R,4S)-4-tert-Butoxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-5-phenyl-pentanoic acid 
• 72155-47-6 N-(tert-butoxycarbonyl)-4(S)-amino-3(R)-hydroxy-5-phenylpentanoic acid ethyl ester 
• 72155-46-5 (3S,4S)-4-(N-tert-butoxycarbonyl)amino-3-hydroxy-5-phenylpentanoic acid ethyl ester 
• 223908-34-7 (4S,3R)-4-(benzyloxycarbonyl-methylamino)-3-hydroxy-5-phenyl-pentanoic acid ethyl ester 
• 223908-31-4 (3S,4S)-4-(Benzyloxycarbonyl-methyl-amino)-3-hydroxy-5-phenyl-pentanoic acid ethyl ester 

Relevant academic research and scientific papers

A Novel, Facile and Diastereoselective Synthesis of (3S,4S) and (3R,4S)-N-Me-AHPPA

Diastereoselective syntheses of (3S,4S) and (3R,4S)-N-methyl-AHPPA are achieved via a novel Wittig reaction of an oxazolidinone followed by reduction.

A novel protocol for N-methyl-γ-amino-β-hydroxy acids from oxazolidinones

A new two step methodology for N-methyl-γ-amino-β-hydroxy acids from oxazolidinones is described.

A novel Wittig reaction of oxazolidinones: Stereospecific synthesis of N-BOC-(3S,4S)-statine and N-BOC-(3S,4S)-AHPPA

Stereospecific synthesis of N-BOC-(3S,4S)-Statine and N-BOC-(3S,4S)- AHPPA is achieved via a novel Wittig reaction of oxazolidinones in an efficient manner.