-
undergo a
decarboxylation process in a
subsequent step. In the so-called
Doebner modification the base is pyridine. For example, the
reaction product of...
- The
Doebner reaction is the
chemical reaction of an
aniline with an
aldehyde and
pyruvic acid to form quinoline-4-carboxylic acids. The
reaction serves...
- The
Doebner–Miller
reaction is the
organic reaction of an
aniline with α,β-unsaturated
carbonyl compounds to form quinolines. This
reaction is also known...
-
second step has occurred, with loss of
carbon dioxide, in the so-called
Doebner modification. Thus, for example, the
reaction product of
acrolein and malonic...
-
anilines and β-ketoesters.
Doebner reaction using anilines with an
aldehyde and
pyruvic acid to form quinoline-4-carboxylic
acids Doebner-Miller
reaction using...
-
better since the
reaction is less violent. Bischler-Napieralski
reaction Doebner-Miller
reaction Skraup, Z. H. (1880). "Eine
Synthese des Chinolins". Berichte...
- Di-π-methane
rearrangement Directed ortho metalation Doebner modification Doebner reaction Doebner–Miller reaction,
Beyer method for
quinolines Doering–LaFlamme...
-
quinoline preparation methods, such as the Conrad-Limpach
synthesis and the
Doebner reaction. It
involves the
condensation of
unsubstituted anilines (1) with...
- King
William Act 1689.
Memoirs of Mary,
Queen of
England edited by R.
Doebner (1886),
quoted in Van der Kiste, p. 138 Van der Kiste, pp. 130–131 Van...
- Causality,
Semigroups and
Rigged Hilbert Spaces, Arno Bohm, Heinz-Dietrich
Doebner,
Piotr Kielanowski, eds., Springer-Verlag, ISBN 3-540-64305-2. (Provides...
