-
following resonance structures.
Enamines can be
easily produced from
commercially available starting reagents.
Commonly enamines are
produced by an acid-catalyzed...
-
ketone or aldehyde.
Since enamines are
generally produced from
ketones or aldehydes, this
overall process (known as the
Stork enamine synthesis) constitutes...
- reason, it
forms a
stable chloramine. It is
commonly used to
generate enamines.
Morpholine is
widely used in
organic synthesis. For example, it is a building...
-
substrates are
dominated by alkenes.
Polar substrates include ketones,
enamines ketimines.
Alkenes that are
particularly amenable to
asymmetric hydrogenation...
- is
widely used to
convert ketones to
enamines.
Enamines derived from
piperidine are
substrates in the
Stork enamine alkylation reaction. Upon treatment...
-
colorless liquid. It is
classified as an
enamine.
Primary and
secondary enamines tend to isomerize, but
tertiary enamines are
kinetically stable. One unusual...
-
alkene must be able to
donate electrons. Such
alkenes are enol
ethers and
enamines. The
reaction product in the
original Povarov reaction is a quinoline....
-
aldehydes toward nucleophilic addition by
formation of
enamines (e.g. used in the
Stork enamine alkylation):
International Union of Pure and
Applied Chemistry...
-
proceed in high
chemical yield under mild conditions. The
intermediate enamines are
electronically related to push–pull olefins,
having an electron-withdrawing...
-
thiourea dioxide,
which features planar amido groups.
Sulfenes react with
enamines, ynamines, and 1,3-cyclopentadienes to give thietanes,
thietes and Diels-Alder...
