Garg, Dimple published the artcileKinetics and mechanism of the oxidation of some α-amino acids by benzyltrimethylammonium tribromide, HPLC of Formula: 111865-47-5, the publication is Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry (2005), 44B(9), 1909-1914, database is CAplus.
The oxidation of nine α-amino acids by benzyltrimethylammonium tribromide (BTMAB), in aqueous acetic acid, gives the corresponding aldehydes. The reaction is first order with respect to BTMAB. Michaelis-Menten type kinetics are observed with respect to the amino acids. The thermodn. parameters for the complex formation and the activation parameters for the decomposition of complex were determined An addition of benzyltrimethylammonium ion does not affect the rate. The oxidation of perdeuterioglycine shows the absence of a kinetic isotope effect (kH/kD = 1.05 at 313 K). The effect of solvent composition indicates that the reaction rate increases with an increase in the polarity of the medium. The reaction is susceptible to both polar and steric effects of the substituents. Suitable mechanism was proposed.
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H16Br3N, HPLC of Formula: 111865-47-5.
Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary