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Tautomers are isomers of organic compounds that readily interconvert by a chemical reaction called tautomerization.

Tautomerism is described in multiple online sources, as addition to our editors' articles, see section below for printable documents, Tautomerism books and related discussion.

Suggested Pdf Resources

Keto-Enol Tautomerism
Keto-Enol Tautomerism. Ketones and aldehydes are in equilibrium with their enol forms.
New light on tautomerism of purines and pyrimidines and its
The tautomerism of the natural 1-substituted pyrimidines and 9-substituted nucleosides which exhibit appreciable tautomerism in solution, e.g.
tautomerism Isomerism of the general form: G–X–Y=Z X=Y–Z–G
where the isomers (called tautomers) are readily interconvertible; the atoms connecting the phenomenon is called ring-chain tautomerism, as in: H O C.
Prototropic Tautomerism Of Heterocycles: Heteroaromatic
Chemical vs Physical Methods for the Study of Tautomerism . . .
Enol-keto tautomerism of a-ketophosphonates
pared and their enol-keto tautomerism has been studied by means ofproton and keto tautomeric forms, with only a small amount of enol forms present.

Suggested News Resources

El supercomputador 'Lusitania' permite estudiar tautometría imina-enamina
Estas investigaciones han dado lugar a una nueva publicación de impacto internacional del grupo de investigación QUOREX, titulada "Tautomerism in Schiff bases.

Suggested Web Resources

Tautomer - Wikipedia, the free encyclopedia
Keto-enol tautomerism - Wikipedia, the free encyclopedia
tautomerism (chemistry) -- Britannica Online Encyclopedia
Keto-Enol Tautomerism
Tautomerism refers to an equilibrium between two different structure of the same compound.
IUPAC Gold Book - tautomerism
Dec 22, 2010 tautomerism. Isomerism of the general form: T06252-1.

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