Results 151 to 160 of about 1,308 (200)
Tricyclic Isatin Derivatives as Anti-Inflammatory Compounds with High Kinase Binding Affinity. [PDF]
Uvarov AV +3 more
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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
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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
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The deuteration of acetanilides
Journal of Labelled Compounds and Radiopharmaceuticals, 1982AbstractThe 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
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Sublimation Enthalpies of 9 Substituted Acetanilides at 298 K Estimated by Solution Calorimetry Approach [PDF]
© 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, 2013Direct 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
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The pharmacokinetics of acetanilide and of diphenylhydantoin sodium
European Journal of Clinical Pharmacology, 1974Acetanilide 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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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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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, 1948B B, BRODIE, J, AXELROD
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