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Polarons in acetanilide

Physical Review B, 1989
The best available data are presented of the integrated intensity of the 1650-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ band in crystalline acetanilide as a function of temperature. A concise theory of polaron states is presented and used to interpret the data.
, Scott, , Bigio, , Johnston
openaire   +2 more sources

The deuteration of acetanilides

Journal of Labelled Compounds and Radiopharmaceuticals, 1982
AbstractThe base‐catalysed exchange of a proton of the methyl groups in acetanilides can be used to incorporate deuterium into these amides. 4′‐Hydroxy‐2[2H]acetanilide (acetaminophen, paracetamol) can be prepared by the demethylation with boron tribromide of 4′‐methoxy‐2[2H]acetamide obtained by this base‐catalysed exchange.
Siow K. Chin   +2 more
openaire   +1 more source

Sublimation Enthalpies of 9 Substituted Acetanilides at 298 K Estimated by Solution Calorimetry Approach [PDF]

open access: yesThermochimica Acta, 2017
© 2017 Elsevier B.V. In this work a solution calorimetry approach was applied for determination of the sublimation enthalpies of 9 substituted acetanilides.
Ruslan N Nagrimanov, Mikhail I Yagofarov
exaly   +1 more source

Oxidative para-Triflation of Acetanilides

Organic Letters, 2013
Direct triflation of acetanilide derivatives with silver triflate has been accomplished under mild iodine(III)-mediated oxidative conditions. The reaction shows excellent regioselectivity for the para position and tolerates a range of ortho and meta substituents on the aromatic ring. This method is also compatible with the preparation of arylnonaflates
Pialat, Amélie   +2 more
openaire   +3 more sources

The pharmacokinetics of acetanilide and of diphenylhydantoin sodium

European Journal of Clinical Pharmacology, 1974
Acetanilide and diphenylhydantoin have a similar first stage biotransformation in that both are oxidized in the para position of the benzene ring incorporated in each of the two molecules.
J L, Cunningham, M F, Bullen, D A, Evans
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Bromination of Acetanilide

Journal of Chemical Education, 1996
A general procedure for bromination of aromatic compounds activated with electron donating substituents such as acetamido, hydroxyl, or ether groups is described. Bromine is generated in situ from potassium bromate and hydrobromic acid. This procedure avoids the hazards associated with direct handling of bromine or bromine solutions.
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THE FATE OF ACETANILIDE IN MAN

The Journal of Pharmacology and Experimental Therapeutics, 1948
B B, BRODIE, J, AXELROD
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Acetanilides

1985
William H. Hallenbeck   +1 more
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