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Org Lett ; 17(19): 4666-9, 2015 Oct 02.
Article in English | MEDLINE | ID: mdl-26381590

ABSTRACT

A regioselective green synthesis of nitroacetaminophen derivatives was carried out by electrochemical oxidation of acetaminophen, N-(2-hydroxyphenyl)acetamide, and 1-(4-(4-hydroxyphenyl)piperazin-1-yl)ethanone in the presence of nitrite ion as a nucleophile. The present work has led to the development of a reagentless green and facile electrochemical method for the synthesis of some nitroacetaminophen derivatives.


Subject(s)
Acetaminophen/analogs & derivatives , Nitrates/chemical synthesis , Acetaminophen/chemical synthesis , Acetaminophen/chemistry , Acetaminophen/pharmacology , Acetanilides/chemistry , Molecular Structure , Nitrates/chemistry , Nitrates/pharmacology , Piperazines/chemistry , Stereoisomerism
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