Chemical Communications,
Journal Year:
2018,
Volume and Issue:
54(65), P. 9087 - 9090
Published: Jan. 1, 2018
By
ruthenium/acid
dual
catalysis,
a
novel
transfer
hydrogenative
para-selective
aminoalkylation
of
aniline
derivatives
with
N-heteroarenes
has
been
demonstrated.
Catalysts,
Journal Year:
2023,
Volume and Issue:
13(3), P. 541 - 541
Published: March 8, 2023
In
the
last
decade,
MOFs
have
been
proposed
as
precursors
of
functional
porous
carbons
with
enhanced
catalytic
performances
by
comparison
other
traditional
carbonaceous
catalysts.
This
area
is
rapidly
growing
mainly
because
great
structural
diversity
offering
almost
infinite
possibilities.
can
be
considered
ideal
platforms
to
prepare
highly
dispersed
metallic
species
or
even
single-metal
atoms
under
strictly
controlled
thermal
conditions.
review
briefly
summarizes
synthetic
strategies
and
MOF-derived
carbons.
The
main
focus
relies
on
application
fine
chemical
synthesis.
Among
most
explored
reactions,
oxidation
reduction
reactions
are
highlighted,
although
some
examples
coupling
multicomponent
also
presented.
However,
this
type
catalyst
in
green
synthesis
biologically
active
heterocyclic
compounds
through
cascade
still
a
challenge.
Green Chemistry,
Journal Year:
2024,
Volume and Issue:
26(7), P. 3786 - 3790
Published: Jan. 1, 2024
A
hitherto
unreported
catalyst-free
ring
expansion
reaction
of
tetrahydroisoquinolines
with
o
-alkynylarylaldehydes
for
the
construction
dibenzo[
b
,
d
]azepine
skeleton
is
described.
Organic Chemistry Frontiers,
Journal Year:
2020,
Volume and Issue:
7(13), P. 1635 - 1639
Published: Jan. 1, 2020
An
efficient
TFA/TBHP-promoted
oxidative
cyclisation
of
readily
available
isatins
with
1,2,3,4-tetrahydroisoquinolines
has
been
firstly
developed.
The
potential
utility
this
strategy
was
demonstrated
by
one-step
synthesis
a
natural
alkaloid
Rutaecarpin.
Advanced Synthesis & Catalysis,
Journal Year:
2024,
Volume and Issue:
366(10), P. 2142 - 2164
Published: Jan. 17, 2024
Abstract
N‐Heterocyclic
compounds,
in
particular,
quinolines
and
quinazolines
are
frequently
used
medicinal
chemistry.
Therefore,
the
direct
clean
synthesis
of
these
valuable
scaffolds
has
been
a
great
interest
for
many
years.
2‐Aminobenzyl
alcohols
as
an
alternative
reactant
instead
unstable
expensive
2‐aminobenzaldehydes
can
be
construction
N‐fused
heterocycles
including
quinolines,
quinazolines,
oxazines,
thiazines,
selenazines,
imidazoles,
diazepines,
etc.
In
this
review
article,
we
have
discussed
recent
developments
use
2‐aminobenzyl
diverse
heterocycles.
Inorganic Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 1, 2025
In
this
study,
an
effective
and
stable
Cu2+
incorporated
within
the
lattice
of
ZIF-8
was
hydrothermally
synthesized
employed
as
a
heterogeneous
catalyst
for
dehydrogenative
coupling
between
2-aminobenzamide
CH3OH.
The
Cu2+-doped
(Cu@ZIF-8)
catalysts
were
firmly
characterized
using
powder
X-ray
diffraction,
Fourier
transform
infrared
spectroscopy,
scanning
electron
microscopy,
transmission
photoelectron
UV-visible
diffuse
reflectance
spectra,
Brunauer-Emmett-Teller
techniques
to
examine
their
structural,
morphological,
elemental,
optical,
surface
properties.
catalytic
efficiency
Cu@ZIF-8
investigated
in
synthesis
quinazolinone
from
CH3OH
C1
source
with
Cs2CO3
base
under
oxygen
atmosphere.
Among
different
catalysts,
30%
demonstrated
superior
activity
formation
compared
pristine
ZIF-8,
indicating
that
doping
ions
provides
synergetic
effect
during
reaction.
Furthermore,
reusability
experiments
carried
out
catalyst,
observed
findings
show
is
maintained
up
four
cycles.
structural
integrity
along
morphology
chemical
structure
reused
solid
also
verified,
no
significant
differences
fresh
solids
plausible
reaction
mechanism
proposed.
Chemical Communications,
Journal Year:
2019,
Volume and Issue:
55(80), P. 12072 - 12075
Published: Jan. 1, 2019
An
efficient
synthesis
of
rutaecarpine
derivatives
via
a
catalyst-free
and
atom-efficiency
cyclization
reaction
between
commercially
available
anthranils
cyclic
amines
is
described.