On the reactivity of organophosphorus compounds. Part III: Application of the Hammett relation to the rates of alkaline hydrolysis of a number of diethyl substituted phenyl phosphates
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/recl.19670860415/fullpdf
Reference20 articles.
1. On the reactivity of organophosphorus compounds. I. The alkaline hydrolysis of some dialkyl p-nitrophenyl phosphates
2. On the reactivity of organophosphorus compounds: II. The effects of structural variations in the alkyl and alkoxy groups on the values of ΔH* and ΔS* for the alkaline hydrolysis of a number of organophosphorus esters
3. Pesticidal Activity and Structure, Structure and Insecticidal Activity of Some Diethyl Substituted Phenyl Phosphates
4. The inhibition of erythrocyte cholinesterase by tri-esters of phosphoric acid. 1. Diethyl p-nitrophenyl phosphate (E 600) and analogues
5. I. Dostrovsky M. Halmann J. Chem. Soc. 502 1953
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