134255-17-7

Upstream product

• 97485-13-7 2-benzamido-3-(4-(benzoyloxy)phenyl)propanoic acid 

Downstream Products

• 134255-18-8 5-benzoylamino-5-p-benzoyloxobenzyl-4-oxo-1,3-dioxane 
• 97512-86-2 Benzoic acid 4-(2-benzoylamino-2-oxo-ethyl)-phenyl ester 
• 55137-55-8 (+)-α-hydroxymethyltyrosine 
• 55137-55-8 (-)-α-hydroxymethyltyrosine 
• 134255-19-9 N-benzoyl-α-hydroxymethyltyrosine 
• 134255-19-9 (-)-N-benzoyl-α-hydroxymethyltyrosine 
• 134255-19-9 (+)-N-benzoyl-α-hydroxymethyltyrosine 

Relevant academic research and scientific papers

Synthesis and absolute configuration of (+) α-hydroxymethyltyrosine by X-ray analysis of its N-benzoyl derivative

α-Hydroxymethyltyrosine has been synthesized by a route involving α-hydroxymethylation.Dextrorotatory N-benzoyl-α-hydroxymethyltyrosine 4 crystallizes in space group P212121 with cell parameters: a = 13.2266(9), b = 16.109

AN EFFICIENT TRANSFORMATION OF N-ACYL-α-AMINO ACIDS INTO DIACYLAMINES VIA 2,4-DISUBSTITUTED OXAZOL-5(4H)-ONES

Base-catalyzed oxygenative decarboxylation of a variety of 2,4-disubstituted oxazol-5(4H)-ones in benzene with triethylamine or in dimethylsulfoxide with potassium tert-butoxide gives diacylamines.KEYWORDS - base-catalyzed autooxidation; selective oxygenation; decarboxylation; oxazol-5(4H)-one; N-acyl-α-amino acid; diacylamine