70985-09-0

Upstream product

• 842-74-0 4-benzylidene-2-phenyloxazole-5(4H)-one 
• 17606-70-1 (4Z)-4-benzylidene-2-phenyl-1,3-oxazol-5(4H)-one 
• 100-52-7 benzaldehyde 
• 98-88-4 benzoyl chloride 
• 5813-81-0 hippuramide 
• 15732-43-1 (E)-2-phenyl-4-benzylidene-5(4H)-oxazolone 

Downstream Products

• 18511-00-7 4-benzylidene-2-phenylimidazol-5(4H)-one 
• 24250-72-4 N-(1-amino-1-oxo-3-phenylpropan-2-yl)benzamide 
• 1643501-30-7 (Z)-N-(3-amino-1-bromo-3-oxo-1-phenylprop-1-en-2-yl)benzamide 
• 132198-57-3 2,5-diphenyloxazole-4-carboxamide 
• 17606-70-1 (4Z)-4-benzylidene-2-phenyl-1,3-oxazol-5(4H)-one 

Relevant academic research and scientific papers

A concise approach to polysubstituted oxazoles from N-acyl-2-bromo enamides via a copper(i)/amino acid-catalyzed intramolecular C-O bond formation

A straightforward and efficient copper(i)/amino acid-catalyzed intramolecular Ullmann-type C-O coupling reaction has been developed. This protocol affords a facile methodology for the synthesis of a series of novel 2,4,5-substituted oxazoles from readily accessible N-acyl-2-bromo enamides under mild conditions. This journal is the Partner Organisations 2014.

A practical and efficient synthesis of 2,5-disubstituted-3,5-dihydro- imidazol-4-ones from oxazolones

An alternative procedure for the synthesis of 2,5-disubstituted-3,5- dihydro-imidazol-4-ones from substituted oxazolones was evaluated. The initial oxazolone ring-opening reaction was examined with a variety of ammonia source compounds followed by the sub

Derivatives of α,β-dehydro amino acids: III. Reaction of 4-arylmethylidene-4,5-dihydro-1,3-oxazol-5-ones with hexamethyldisilazane

4-Arylmethylidene-4,5-dihydro-1,3-oxazol-5-ones reacted with hexamethyldisilazane in ethyl acetate, acetonitrile, or DMF at room temperature to give mainly 2-acylamino-3-arylmethylideneprop-2-enamides, whereas in boiling DMF the corresponding 4-arylmethyl

A new synthetic route to 4-arylidene-2-phenyl-2-imidazolin-5-ones

Condensation of aromatic aldehydes with benzoylglycine amide in saturated potassium carbonate solution yields imidazolinones 2. Eight imidazolinones have been synthesized by this method in 4460% yields. The reaction follows pathway (i) which has been prov

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.

Asymmetric Hydrogenation with Chiral Aminophosphine-Rhodium Complexes and Chiral Recognition by Bisphosphine-Rhodium Complexes in the Asymmetric Hydrogenation of Olefins through the Chiral Helical Conformation of Phenyl Groups on the Phosphorus Atom

The asymmetric hydrogenation of α-acylaminocinnamic acids with the rhodium complex of (1R,2R)-1,2-bis(N-diphenylphosphino-N-methylamino)cyclohexane has been reported to give preferentially (S)-amino acids.On the contrary, it has been found that the enanti