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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Recueil des Travaux ...arrow_drop_down
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Recueil des Travaux Chimiques des Pays-Bas
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Amides II. Acylation of amides to diacylimines

Authors: J. B. Polya; T. M. Spotswood;

Amides II. Acylation of amides to diacylimines

Abstract

AbstractThree acylating mechanisms are involved in the reaction between amides and anhydrides. In the aliphatic series all mechanisms are governed by the inductive effects operating in the reactants.Amides act as acids towards anhydrides.Diacylimines and the corresponding anhydrides acylate alcohols by the same mechanism.A new compound, propionylchloroacetamide, has been prepared. Properties of some diacylimines have been established. Uses for diacylimines are suggested.

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
21
Average
Top 10%
Average
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