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dc.contributor.authorThennarasu, S-
dc.contributor.authorPerumal, P T-
dc.date.accessioned2013-11-27T04:49:12Z-
dc.date.available2013-11-27T04:49:12Z-
dc.date.issued2001-12-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/24263-
dc.description1174-1176en_US
dc.description.abstractAn 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.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.40B(12) December 2001]en_US
dc.titleSynthesis of new hydantoins as intermediates for diamino acidsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.40B(12) December 2001]

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