Green Chemistry,
Journal Year:
2023,
Volume and Issue:
25(8), P. 3117 - 3126
Published: Jan. 1, 2023
Using
ball
milled
CNT
catalysts,
the
electrocatalytic
reductive
amination
of
keto
acids
to
amino
was
efficiently
conducted.
Moderate
high
formation
rates
(up
180.9
mmol
g
−1
cat
h
)
and
Faradaic
efficiencies
90%)
were
achieved.
Catalysis Science & Technology,
Journal Year:
2022,
Volume and Issue:
12(22), P. 6623 - 6649
Published: Jan. 1, 2022
In
this
review
the
concept
of
bridging
homogeneous
and
heterogeneous
catalysis
aspects
for
preparation
nanoparticle-,
single
atom-
supported
metal
complex-based
catalysts
their
applications
in
organic
transformations
is
discussed.
ChemSusChem,
Journal Year:
2022,
Volume and Issue:
15(7)
Published: Feb. 16, 2022
Abstract
One‐pot
synthesis
of
sustainable
primary
amines
by
catalytic
reductive
amination
bio‐based
carbonyl
compounds
with
NH
3
and
H
2
is
emerging
as
a
promising
robust
approach.
The
amines,
especially
furfuryl
amine
(FUA)
derived
from
furfural
(FUR),
wide
range
applications
pharmaceuticals
to
agrochemicals,
have
attracted
much
attention
due
their
versatility.
This
Review
majorly
comprised
two
segments
on
the
FUR
FUA,
one
precious
(Ru,
Pd,
Rh)
other
non‐precious
(Co,
Ni)
metals
different
supports
in
various
solvent
systems
presence
.
active
metal
sites
generated
multiple
are
accentuated
experimental
evidence
based
CO‐diffuse
reflectance
infrared
Fourier‐transform
spectroscopy,
temperature‐programmed
reduction,
X‐ray
photoelectron
calorimetry.
Moreover,
this
comprehensively
describes
role
acidic
basic
support
for
yield
FUA.
Overall,
provides
an
insight
into
how
design
develop
efficiently
catalyst
selective
broad
spectrum
corresponding
amines.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Oct. 10, 2023
The
sustainable
production
of
value-added
N-heterocycles
from
available
biomass
allows
to
reduce
the
reliance
on
fossil
resources
and
creates
possibilities
for
economically
ecologically
improved
synthesis
fine
bulk
chemicals.
Herein,
we
present
a
unique
Ru1CoNP/HAP
surface
single-atom
alloy
(SSAA)
catalyst,
which
enables
new
type
transformation
bio-based
platform
chemical
furfural
give
N-heterocyclic
piperidine.
In
presence
NH3
H2,
desired
product
is
formed
under
mild
conditions
with
yield
up
93%.
Kinetic
studies
show
that
formation
piperidine
proceeds
via
series
reaction
steps.
Initially,
in
this
cascade
process,
amination
furfurylamine
takes
place,
followed
by
hydrogenation
tetrahydrofurfurylamine
(THFAM)
then
ring
rearrangement
DFT
calculations
suggest
Ru1CoNP
SSAA
structure
facilitates
direct
opening
THFAM
resulting
5-amino-1-pentanol
quickly
converted
value
presented
catalytic
strategy
highlighted
an
actual
drug,
alkylated
piperidines,
pyridine.
nitrogen-containing
heterocycles
scarcely
known.
Here,
authors
report
piperidines
one-pot
utilizing
catalyst.
Green Chemistry,
Journal Year:
2023,
Volume and Issue:
25(8), P. 3117 - 3126
Published: Jan. 1, 2023
Using
ball
milled
CNT
catalysts,
the
electrocatalytic
reductive
amination
of
keto
acids
to
amino
was
efficiently
conducted.
Moderate
high
formation
rates
(up
180.9
mmol
g
−1
cat
h
)
and
Faradaic
efficiencies
90%)
were
achieved.