-
between aldimines and ketimines,
derived from
aldehydes and ketones, respectively. In
imines the five core
atoms (C2C=NX, ketimine; and C(H)C=NX,
aldimine; X...
- acids. The
aldehyde group of PLP
forms a Schiff-base
linkage (internal
aldimine) with the ε-amino
group of a
specific lysine group of the aminotransferase...
-
Internal aldimine formation: First, the ε-amino
group of Lys258
forms a
Schiff base
linkage with the
aldehyde carbon to
generate an
internal aldimine. Transaldimination:...
- the
aldimine-tin chloride,
washing it with
ether and then
hydrolyzing it. However, it has been
found that this step is
unnecessary and the
aldimine tin...
-
starting from
TosMIC and an
aldimine. The Van
Leusen Imidazole Synthesis allows the
preparation of
imidazoles from
aldimines by
reaction with tosylmethyl...
-
resulting in the
release of cysteine. The
lysine residue reforms the
internal aldimine by
kicking off α-iminobutyric acid.
Afterwards the
external ketimine is...
- a sub-class of imines,
being either secondary ketimines or
secondary aldimines depending on
their structure. Anil
refers to a
common subset of Schiff...
- {\ce {RC(=NR'')R'}}} imino- -imine
Primary aldimine RC(=NH)H imino- -imine
Ethanimine Secondary aldimine RC(=NR')H imino- -imine
Imide Imide (RCO)2NR'...
-
aromatic amine groups then
react with the
aldehyde being tested to form two
aldimine groups;
these groups have also been
named for
their discoverer as Schiff...
-
occur readily. Upon quenching, the
resulting molecule is an oxazole. If an
aldimine is used,
formed from the
condensation of an
aldehyde with an amine, then...
