75040-62-9Relevant academic research and scientific papers
Monomeric Methyl Metaphosphate: Reactions with Carbonyl Groups
Satterthwait, Arnold C.,Westheimer, F. H.
, p. 4464 - 4472 (2007/10/02)
Monomeric methyl metaphosphate, generated by fragmentation of methyl hydrogen erythro-1-phenyl-1,2-dibromopropylphosphonate in the presence of 2,2,6,6-tetramethylpiperidine, can be identified by its electrophilic attack on the aromatic rings of substituted anilines.The aromatic substitution reactions are quenched by pyridine, acetonitrile, dioxane, and dimethoxyethane but not by chloroform.Monomeric methyl metaphosphate attacks acetophenone to yield an enol phosphate; it converts a mixture of o-trifluoromethylaniline and acetophenone into N-(1-methylbenzylidene)-2-aminobenzotrifluoride and also converts aniline and ethyl benzoate into O-ethyl-N-phenylbenzimidate.These latter reactions mimic enzymatic reactions that require ATP.These facts introduce the possibility that ATP plays a kinetic role as well as a thermodynamic one in metabolic processes.
SOLVOLYSIS OF DIPHENYL AMIDOPHOSPHATES IN AQUEOUS ALCOHOLIC MEDIA
Kasparek, Frantisek,Mollin, Jiri
, p. 386 - 396 (2007/10/02)
Influence of substituent on the reaction rate of the alkali-catalyzed solvolysis of the studied compounds set has been followed.The activation entropy has also been determined.The reaction products have been identified, and their concentration ratio has been determined.The reaction selectivity is mostly influenced by sterical effects in the substrate molecule.The results obtained agree with the SN2 mechanism.
