-
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;...
- intermediate.
Ketimine formation: The qui****id is reprotonated, but now at the
aldehyde carbon, to form the
ketimine intermediate.
Ketimine hydrolysis:...
-
Lanthionine ketimine (3,4-dihydro-2H-1,3-thiazine-3,5-dicarboxylic acid) is a
naturally occurring sulfur amino acid
metabolite found in the
mammalian brain...
- The
ketimine Mannich reaction is an
asymmetric synthetic technique using differences in
starting material to push a
Mannich reaction to
create an enantiomeric...
-
volatile and
flammable liquid at room temperature. It is the
simplest ketimine. This
compound is
mainly of
academic interest.
Acetone imine is prepared...
- + H2O → (C6H5)2C=NH + MgBr(OH) This
method is
known as Moureu-Mignonac
ketimine synthesis. Yet
another route to
benzophenone imine involves reaction of...
-
nitriles can be
prepared from base
hydrolysis of
trichloromethyl aryl
ketimines (RC(CCl3)=NH) in the Houben-Fischer
synthesis Nitriles can be obtained...
-
intermediate accepts a
proton at a
different position to
become a
ketimine. The
resulting ketimine is
hydrolysed so that the
amino group remains on the complex...
- They can be
considered a sub-class of imines,
being either secondary ketimines or
secondary aldimines depending on
their structure. Anil
refers to a...
- but
sometimes bound through the
central carbon only, see also
analogous ketimine analogues Alkenes R2C=CR2
neutral compounds with a C−C
double bond Aminopolycarboxylic...
