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- Q4727741 subject Q7400695.
- Q4727741 abstract "Alkylimino-de-oxo-bisubstitution in organic chemistry is the organic reaction of carbonyl compounds with amines to imines. The reaction name is based on the IUPAC Nomenclature for Transformations. The reaction is acid catalyzed and the reaction type is nucleophilic addition of the amine to the carbonyl compound followed by transfer of a proton from nitrogen to oxygen to a stable hemiaminal or carbinolamine. With primary amines water is lost in an elimination reaction to an imine. With aryl amines especially stable Schiff bases are formed.".
- Q4727741 thumbnail N-Ethylidenecyclohexylamine.svg?width=300.
- Q4727741 wikiPageExternalLink m435.htm.
- Q4727741 wikiPageExternalLink prep.asp?prep=cv6p0818.
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- Q4727741 wikiPageWikiLink Q101487.
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- Q4727741 wikiPageWikiLink Q7400695.
- Q4727741 wikiPageWikiLink Q898525.
- Q4727741 wikiPageWikiLink Q901669.
- Q4727741 wikiPageWikiLink Q910229.
- Q4727741 comment "Alkylimino-de-oxo-bisubstitution in organic chemistry is the organic reaction of carbonyl compounds with amines to imines. The reaction name is based on the IUPAC Nomenclature for Transformations. The reaction is acid catalyzed and the reaction type is nucleophilic addition of the amine to the carbonyl compound followed by transfer of a proton from nitrogen to oxygen to a stable hemiaminal or carbinolamine. With primary amines water is lost in an elimination reaction to an imine.".
- Q4727741 label "Alkylimino-de-oxo-bisubstitution".
- Q4727741 depiction N-Ethylidenecyclohexylamine.svg.