- In
organic chemistry, the Arndt–
Eistert reaction is the
conversion of a
carboxylic acid to its homologue. It is
named for the
German chemists Fritz Arndt...
-
intermediate with
nucleophiles to form
carboxylic acid derivatives. The Arndt-
Eistert homologation is a
specific example of this use,
wherein a
carboxylic acid...
-
Bernd Eistert (9
November 1902 – 22 May 1978) was a
German chemist.
Together with
Fritz Arndt he
discovered the Arndt-
Eistert synthesis.
Eistert was born...
- methoxymethylenetriphenylphosphine,
which produces a
homologous aldehyde. Arndt–
Eistert reaction is a
series of
chemical reactions designed to
convert a carboxylic...
- the
chain shortened by one carbon. The
inverse procedure is the Arndt–
Eistert synthesis,
where an acid is
converted into acyl halide,
which is then reacted...
- from the acyl
chloride (by
treatment with
thionyl chloride) via a Arndt–
Eistert reaction with
diazomethane then by
treatment with pot****ium phthalimide...
-
acids have been
prepared by many routes,
including some
based on the Arndt-
Eistert synthesis.
Because their backbones are
longer than
those of
normal peptides...
-
contributions to
synthetic methodology, who
together with
Bernd Eistert discovered the Arndt-
Eistert synthesis.
Fritz Arndt was born on 6 July 1885, in Hamburg...
- esters. This
reaction was
designed as a
safer alternative to the Arndt–
Eistert synthesis,
avoiding the need for diazomethane. The
Kowalski reaction is...
- acyl
halide and diazomethane, for
example the
first step in the Arndt-
Eistert synthesis. In
diazo transfer certain carbon acids react with
tosyl azide...
