-
proximity that
their reactivity is changed, such as 1,2-, 1,3-, and 1,4-
dicarbonyls.
Their properties often differ from
those of monocarbonyls, and so they...
-
through the
Claisen condensation, or 1,5-
dicarbonyls,
which are
commonly made
using a
Michael reaction, 1,4-
dicarbonyls are
challenging substrates to synthesize...
-
Malondialdehyde belong to the
class of β-
dicarbonyls. A
colorless liquid,
malondialdehyde is a
highly reactive compound that
occurs as the enol. It is...
-
further dehydration and
deamination to
produce dicarbonyls. This is a
crucial intermediate.
Dicarbonyls react with
amines to
produce Strecker aldehydes...
- and its
amide derivatives feature the
acryloyl group. α,β-Unsaturated
dicarbonyls are also common. The
parent compounds are
maleic acid and the isomeric...
-
glucosepane through an α-
dicarbonyl intermediate. The
particular reaction path
proceeding from the
Amadori product to the α-
dicarbonyl intermediate that will...
-
sulfurization of a
dicarbonyl,
producing a thioketone. The Paal–Knorr
reaction is
quite versatile. In all
syntheses almost all
dicarbonyls can be converted...
-
IUPAC name Benzene-1,4-
dicarbonyl dichloride Other names Terephthaloyl dichloride 1,4-Benzenedicarbonyl
chloride Benzene-1,4-
dicarbonyl chloride Terephthalic...
-
Cyclopentadienyliron dicarbonyl dimer is an
organometallic compound with the
formula [(η5-C5H5)Fe(CO)2]2,
often abbreviated to Cp2Fe2(CO)4, [CpFe(CO)2]2...
-
positive test with hydrazines, hydrazones, α-hydroxy
ketones and 1,2-
dicarbonyls. Both Tollens'
reagent and Fehling's
reagent give
positive results with...
