- bases:
imines derived from anilines. The term can be
synonymous with
azomethine which refers specifically to
secondary aldimines (i.e. R−CH=NR' where...
-
Azomethine ylides are nitrogen-based 1,3-dipoles,
consisting of an
iminium ion next to a carbanion. They are used in 1,3-dipolar
cycloaddition reactions...
- (R2CN(R)O) Some imines:
Azomethine imine Nitrilimines (RCN−NR,
analogous to
nitrile oxide)
Carbonyl imines Some
ylides Azomethine ylide Nitrile ylide (RCNCR'2)...
-
dipole or a
nucleophilic dipole,
which includes azomethine ylide,
carbonyl ylide,
nitrile ylide,
azomethine imine,
carbonyl imine and diazoalkane. These...
-
primary amines,
ferrocenecarboxaldehyde condenses to give imines. The
azomethine derivative undergoes 1,3-cycloaddition to C60. It can be
reduced to the...
-
electrophilic carbenes.
Certain nitrogen-based
ylides also
exist such as
azomethine ylides with the
general structure:
These compounds can be
envisioned as...
-
electron transfer),
organic electronics,
switching and sensing.
Amphoterism Azomethine ylide "Zwitterion".
Chemistry LibreTexts. 2015-11-03.
Archived from the...
-
possible side-reactions: the
ketone and
proline to an oxazolidinone; and two
copies of the
aldehyde and
proline decarboxylating to an
azomethine ylide....
-
imine Names Preferred IUPAC name
Methanimine Other names Formaldimine Azomethine Formaldehyde imine Identifiers CAS
Number 2053-29-4 3D
model (JSmol) Interactive...
- Vedejs, E.; Grissom, J. W. (1988). "4-Oxazoline
route to
stabilized azomethine ylides.
Controlled reduction of
oxazolium salts".
Journal of the American...
