1-ARYL-5-CARBOXYMETHYLHYDANTOIN DERIVATIVES. STRUCTURE OF 1-PHENYL-2-THIO-5-CARBOMETHOXYMETHYLHYDANTOIN
The reaction of aromatic amines with maleic acid or its diethyl ester with subsequent hydrolysis gave N-arylaspartic acids, which were converted to 1-aryl- and 1-aryl-2-thio-5-carboxymethylhydantoins by the action of urea, cyanates, or thiocyanates in an
Baltrushis, R. S.,Beresnevichyus, Z.-I. G.,Vizgaitis, I. M.,Gatilov, Yu. V.
p. 1226 - 1231
(2007/10/02)
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