1026149-22-3Relevant academic research and scientific papers
Reaction of 4-ethoxycarbonyl-2-phenyl-4,5-dihydrooxazol-5-one with organolead(IV) triacetates. A route to some α-arylglycine and α-vinylglycine derivatives
Koen, Mark J.,Morgan, Jacqueline,Pinhey, John T.,Sherry, Christopher J.
, p. 487 - 491 (2007/10/03)
4-Ethoxycarbonyl-2-phenyl-4,5-dihydrooxazol-5-one undergoes rapid arylation and vinylation with arylead triacetates and (E)-styryllead triacetates, respectively. The resulting moisture-sensitive 4-aryl- and 4-styryl-oxazolones undergo hydrolysis and decar
Arylation of 4-Ethoxycarbonyl-2-phenyloxazol-5-one by Aryllead Triacetates: A Convenient Route to α-Arylglycines
Koen, Mark J.,Morgan, Jacqueline,Pinhey, John T.
, p. 2383 - 2384 (2007/10/02)
4-Ethoxycarbonyl-2-phenyloxazol-5-one, which exists in chloroform as the enol 2, undergoes rapid arylation under very mild conditions with aryllead(IV) triacetates to give almost quantitative yields of 4-aryl-4-ethoxycarbonyl-2-phenyloxazol-5-ones 3, whic
