-
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...
-
further dehydration and
deamination to
produce dicarbonyls. This is a
crucial intermediate.
Dicarbonyls react with
amines to
produce Strecker aldehydes...
-
Malondialdehyde belong to the
class of β-
dicarbonyls. A
colorless liquid,
malondialdehyde is a
highly reactive compound that
occurs as the enol. It is...
-
through the
Claisen condensation, or 1,5-
dicarbonyls,
which are
commonly made
using a
Michael reaction, 1,4-
dicarbonyls are
challenging substrates to synthesize...
-
Cyclopentadienyliron dicarbonyl methyl is an
organoiron complex with the
formula (C5H5)Fe(CO)2CH3. It is an
orange volatile solid that is
sensitve to air...
- and its
amide derivatives feature the
acryloyl group. α,β-Unsaturated
dicarbonyls are also common. The
parent compounds are
maleic acid and the isomeric...
-
sulfurization of a
dicarbonyl,
producing a thioketone. The Paal–Knorr
reaction is
quite versatile. In all
syntheses almost all
dicarbonyls can be converted...
- chemistry; it
contains iron in the −2
oxidation state.
Cyclopentadienyliron dicarbonyl dimer contains iron in the rare +1
oxidation state. A
landmark in this...
-
IUPAC name Benzene-1,4-
dicarbonyl dichloride Other names Terephthaloyl dichloride 1,4-Benzenedicarbonyl
chloride Benzene-1,4-
dicarbonyl chloride Terephthalic...
-
Cyclopentadienylcobalt dicarbonyl is an
organocobalt compound with
formula (C5H5)Co(CO)2,
abbreviated CpCo(CO)2. It is an
example of a half-sandwich complex...
