142924-43-4Relevant articles and documents
UEBERFUEHRUNG VON N-ACYLAMINOSAEUREN IN ENAMINE DURCH BECKMAN-FRAGMENTIERUNG VON α-ACYLAMINOKETOXIMEN
Redeker, Ursula,Engel, Norbert,Steglich, Wolfgang
, p. 4263 - 4264 (1981)
A three-step sequence is described which permits conversion of N-acylamino acids and N-acylpeptides into the corresponding enamides.
Synthesis of new hydantoins as intermediates for diamino acids
Thennarasu,Perumal
, p. 1174 - 1176 (2007/10/03)
An efficient and convenient procedure involving microwave and ultrasound conditions for the synthesis of 5,5-disubstituted hydantoins is reported. The combined use of microwave and ultrasound reduces the reaction time significantly. In the presence of potassium cyanide and ammonium carbonate, the acetyl ester bond is hydrolysed under both ultrasonic and reflux conditions.