5235-63-2Relevant academic research and scientific papers
SN2 Reactions of a Carbon Nucleophile with N-Aryl-O-pivaloylhydroxylamines: A Model for in Vivo Reactions of Carcinogenic Metabolites of Aromatic Amines
Novak, Michael,Martin, Kristy A.,Heinrich, Julie L.
, p. 5430 - 5431 (2007/10/02)
The reaction of the N-aryl-O-pivaloylhydroxylamines 3a-c with N,N-dimethylaniline 4 to generate the diphenylamines 5a-c and 6a-c, a model for the in vivo reaction of similar esters of carcinogenic N-arylhydroxylamines with C-8 of quanosine, proceeds via a
Stabilization of unsaturated carboxylic acid esters with mixtures of polyalkylene-amines and arylenediamines
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, (2008/06/13)
A method of inhibiting polymerization of unsaturated carboxylic acid esters and improved unsaturated carboxylic acid ester compositions are described. The method comprises, and the compositions are prepared by, incorporating into the ester composition a combination comprising polyalkyleneamine and arylenediamine of the formula STR1 in which X is hydrogen, chloro, trichloromethyl, trifluoromethyl, nitro, lower alkyl, lower alkoxy or phenoxy, R is hydrogen or alkyl, and R1 is alkyl or phenyl or R and R1 together with the nitrogen atom is a heterocycle selected from the group consisting of pyrrolidinyl, 2,5-dimethyl pyrrolidinyl, piperidino and hexahydro-1H-azepin-1-yl.
