2009
DOI: 10.1007/s11243-009-9225-9
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Kinetics and mechanism of oxidation of β-Alanine by N-bromophthalimide in the presence of Ru(III) chloride as homogenous catalyst in acidic medium

Abstract: The kinetics of Ru(III) chloride-catalyzed oxidation of b-Alanine (NH 3 ? CH 2 CH 2 COOH, b-Ala) by Nbromophthalimide (NBP) in aqueous perchloric acid medium was studied at 35°C. The rate law followed a first-order and zero-order dependence with respect to [NBP] and [b-Ala], respectively. The reaction followed first-order kinetics with respect to [Ru(III)] chloride at a range of low concentrations while the order changed from first-to zero-order at high concentration of [Ru(III)] chloride; demonstrating the c… Show more

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Cited by 18 publications
(17 citation statements)
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“…have been extensively developed for use in organic synthesis, which includes N-haloamines, N-haloamides, N- N-haloureas, N-halosaccharins, N-halosulfonamides, N-halosulfonimides in general, and Nhalosuccinimides (>N-X, Where X= Cl, Br, I etc.) in particular [31][32][33][34][35][36][37] . This is supported by the fact that Nhalocompounds are good sources of halonium cations (X + ), hypohalite species (HOX) and nitrogen anions.…”
Section: -30mentioning
confidence: 99%
“…have been extensively developed for use in organic synthesis, which includes N-haloamines, N-haloamides, N- N-haloureas, N-halosaccharins, N-halosulfonamides, N-halosulfonimides in general, and Nhalosuccinimides (>N-X, Where X= Cl, Br, I etc.) in particular [31][32][33][34][35][36][37] . This is supported by the fact that Nhalocompounds are good sources of halonium cations (X + ), hypohalite species (HOX) and nitrogen anions.…”
Section: -30mentioning
confidence: 99%
“…[1,2] In recent development NCS has been extensively employed as an oxidant for a variety of organic substrates, [3] chalcones, [4] 2-hydroxy propanoic acid [5] (in alkaline medium) 9-telluraheptadecanoic acid, [6] alcohols, [7] benzyl phenyl ether [8] etc.…”
Section: Introductionmentioning
confidence: 99%
“…Acetals are etherification products of alcohols and aldehydes. [1][2][3] Generallyacetals result from elimination of one molecule of water from one molecule of carbonyl compound and two molecules of an alcohol. RCHO + 2R'OHRCH (OR') 2 + H 2 O Aldehydes and alcohols are very sensitive to oxidizing agents in alkaline media.…”
Section: Introductionmentioning
confidence: 99%