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dc.contributor.authorRamachandran, M S-
dc.contributor.authorEaswaramoorthy, D-
dc.contributor.authorSayeekannan, R-
dc.contributor.authorVasanthkumar, S-
dc.date.accessioned2017-04-24T06:16:55Z-
dc.date.available2017-04-24T06:16:55Z-
dc.date.issued1996-08-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/41400-
dc.description696-700en_US
dc.description.abstractThe kinetics of oxidation of amino acids by bromine in aqueous, perchloric acid medium at 35°C has been studied. Based on the experimental results, a reaction scheme is proposed in which the active oxidants are bromine and HOBr. The electrophilic attack of bromine occurs at the carboxylate (- COO -) group. HOBr reacts with the amino acids through the a-hydrogen atom via hydride ion transfer or abstraction. The a-substituent plays a vital role in accelerating the rate limiting step.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-A Vol.35A(08) [August 1996]en_US
dc.titleRole of a-substituent on the oxidation of a-amino acids by bromine in acid mediumen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.35A(08) [August 1996]

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