93634-60-7

Upstream product

• 7152-75-2 (Z)-2-phenyl-4-(4-nitrobenzylidene)-(4H)-1,3-oxazol-5-one 
• 64-17-5 ethanol 
• 93634-58-3 2-benzoylamino-3-(4-nitrophenyl)acrylic acid 
• 7152-75-2 4-(4-nitrobenzylidene)-2-phenyl-5(4H) oxazolone 
• 84337-81-5 3-ethoxy-2-benzamido-3-oxopropanoic acid 
• 555-16-8 4-nitrobenzaldehdye 
• 96-86-6 diethyl benzamidomalonate 
• 495-69-2 Hippuric Acid 

Downstream Products

• 68199-91-7 4-amino-N-benzoyl-DL-phenylalanine ethyl ester 
• 1394232-49-5 ethyl (5Z)-5-(cyclohexylimino)-4-(4-nitrobenzyl)-2-phenyl-4,5-dihydro-1,3-oxazole-4-carboxylate 
• 877036-05-0 4-amino-N-benzoyl-DL-phenylalanine 
• 2922-41-0 (p-aminophenyl)alanine 

Relevant academic research and scientific papers

Stereoselective synthesis of dehydroamino acids using malonic acid half oxyester and aromatic aldehydes

An efficient and direct approach was developed for the synthesis of α,β-dehydroamino acid derivatives with a broad range of substrates. Amido-substituted Malonic Acid Half Oxyesters (MAHOs) have proven to be excellent partners of various aromatic aldehyde

Diastereoselective synthesis of 5-iminooxazolines and their subsequent transformation to α,α-disubstituted dipeptide esters: A formal [4+1] cycloaddition reaction of cyclohexyl isocyanide and Z-alkyl-α-benzoyl amino-acrylates

A novel atom economical diastereoselective synthesis of 5-iminooxazolines and their subsequent transformation to α,α-disubstituted dipeptide esters is described. Heating a mixture of cyclohexyl isocyanide and Z-α-benzoyl amino-acrylic acid alkyl esters un

The use of cyclohexyl isocyanide in the esterification of N-benzoyl α-amino acids derivatives

The N-benzoyl of α,β-dehydroamino acids that were obtained by condensation of N-benzoylglycine and an aldehyde, were esterified with an alcohol in high yield using cyclohexyl isocyanide to activate the carboxylic acid under neutral conditions.

A new methodology for the synthesis of N-acylaminocinnamates

A new synthesis of biologically active N-protected amino acids (2) and amides (4) from 4-ylidene-5(4H)-oxazolones (1) is described.

TRIETHYLAMINE, ETHANOL- MEDIATED DISCIPLINED REACTIONS OF S-BENZYLISOTHIOURONIUM CHLORIDE WITH UNSATURATED 2-OXAZOLIN-5-ONES: SYNTHESIS OF (Z)-2-AMINO-4-ARYLMETHYLENE-2-IMIDAZOLIN-5-ONES, 5-BENZOYLAMINO-2-BENZYLTHIO-6-OXO-4,4-SPIROCYCLOHEXYL-1,4,5,6-TETRA

Triethylamine-mediated condensation of S-benzylisothiouronium chloride with (Z)-4-arylmethylene-2-phenyl-2-oxazolin-5-ones (4) in ethanol gives (Z)-2-amino-4-arylmethylene-2-imidazolin-5-ones (7), whereas the similar reaction with 4-cyclohexylidene-2-phen