The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 18, 2024
A
facile,
cost-effective,
and
sustainable
synthesis
of
substituted
triazines
from
primary
alcohols
by
newly
synthesized
nickel
pincer-type
complexes
(1–3)
has
been
described.
Herein,
we
report
the
a
set
three
well-defined
Ni(II)
O^N^O
complexes,
structurally
characterized
analytical,
spectral,
X-ray
diffraction
techniques.
Further,
are
explored
as
efficient
catalysts
(4
mol
%)
for
construction
2,4,6-substituted
1,3,5-triazines
readily
available
via
an
acceptorless
dehydrogenative
coupling
(ADC)
strategy.
wide
range
triazine
derivatives
(33
examples)
benzamidine/guanidine
hydrochloride
with
maximum
isolated
yield
92%
under
mild
conditions,
eco-friendly
H2O
H2
gas
only
byproducts.
plausible
mechanism
proposed
based
on
sequence
control
experiments.
Interestingly,
short
antiulcer
drug
irsogladine
large-scale
2,4-diphenyl-6-(p-tolyl)-1,3,5-triazine
highlight
convenience
current
methodology.
Dalton Transactions,
Год журнала:
2022,
Номер
51(43), С. 16688 - 16705
Опубликована: Янв. 1, 2022
Two
novel
halogenated
(Br-
and
F-)
quinazoline
derivatives,
namely
[(E)-4-(2-((6-bromopyridin-2-yl)methylene)hydrazinyl)quinazoline]
(L1)
[(E)-4-(2-((3-fluoropyridin-2-yl)methylene)hydrazinyl)
quinazoline]
(L2),
were
synthesized
characterized.
Their
interaction
with
a
series
of
metal(II)
ions
(=
Mn(II),
Ni(II),
Cu(II),
Zn(II)
Cd(II))
resulted
in
the
formation
six
mononuclear
complexes
characterized
by
spectroscopic
techniques
single-crystal
X-ray
crystallography.
The
bear
formulae
[Ni(L1)2](NO3)2
(1),
[Zn(L2)2](NO3)(PF6)
(2),
[Cd(L2)(H2O)(CH3OH)(NO3)](NO3)
(3),
[Cu(L2)Cl2]
(4),
[Ni(L2)2](NO3)2
(5)
[Mn(L2)(CH3OH)(Cl)2]
(6).
biological
activity
compounds
was
further
evaluated
vitro
regarding
their
calf-thymus
DNA,
cleavage
ability
towards
supercoiled
circular
pBR322
plasmid
DNA
absence
or
presence
irradiation
at
various
wavelengths
(UVA,
UVB
visible
light),
affinity
to
bovine
serum
albumin
scavenge
1,1-diphenyl-picrylhydrazyl
2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic
acid)
radicals
reduce
H2O2.
In
silico
molecular
docking
calculations
employed
study
behavior
albumin.
The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
89(16), С. 11161 - 11172
Опубликована: Июль 31, 2024
A
sustainable
catalytic
synthesis
of
selective
monoalkylated
amines
from
nitroarenes
and
alcohols
by
new
palladium(II)-NNO
pincer-type
complexes
has
been
described.
Herein,
a
series
Pd(II)
[Pd(NNO)PPh
Dalton Transactions,
Год журнала:
2023,
Номер
52(32), С. 11104 - 11112
Опубликована: Янв. 1, 2023
A
series
of
hydrazone-based
N,O-chelate
half-sandwich
iridium
complexes
were
synthesized
through
a
facile
route
with
good
yields.
These
air-
and
moisture-stable
exhibited
excellent
catalytic
activity
in
the
cyanosilylether
synthesis
under
mild
reaction
conditions.
Under
catalysis
iridium,
various
cyanosilylethers
different
substituents
obtained
one-pot
trimethylsilyl
cyanide
(TMSCN)
carbonyl
substrates,
to
The
efficiency,
wide
substrate
range,
conditions
made
this
type
catalyst
have
potential
for
industrial
applications.
All
well
characterized
by
IR,
NMR,
EA
analyses.
molecular
structure
complex
1
was
confirmed
single-crystal
X-ray
analysis.
Applied Organometallic Chemistry,
Год журнала:
2023,
Номер
37(10)
Опубликована: Авг. 22, 2023
The
development
of
green,
sustainable,
and
atom‐economical
procedure
for
the
construction
amides
via
C‐N
bond
formation
is
a
high
priority
in
synthetic
organic
community.
In
this
research
article,
we
demonstrate
simple
an
efficient
catalytic
protocol
N‐alkylation
benzamides/sulfonamides
using
aromatic
primary
alcohols
as
coupling
partners
through
borrowing
hydrogen
(BH)
strategy
by
employing
newly
constructed
palladium
(II)
O^N^O
pincer
complexes.
All
complexes
are
characterized
analytical
spectral
methods
(FT‐IR,
NMR,
HRMS).
Further,
solid‐state
molecular
structures
have
been
well
authenticated
single‐crystal
XRD
studies.
present
facile,
worked
low
catalyst
loading
(0.5
mol%),
furnishes
desired
N‐alkyl
with
excellent
yields
up
to
92%.
methodology,
reaction
proceeds
intermediates
such
aldehyde
(E)‐N‐benzylidenebenzamide
release
water
ecological
by‐product.
control
experiments
plausible
mechanistic
investigations
suggested
that
was
initially
dehydrogenation
alcohol
generate
alkylated
products
auto‐transfer.
A
large‐scale
synthesis
N‐(4‐methoxybenzyl)benzamide
proves
effectiveness
Pd
catalysts.
Chemistry - An Asian Journal,
Год журнала:
2023,
Номер
18(22)
Опубликована: Окт. 10, 2023
Acyl
hydrazones
are
a
class
of
synthetically
important
organic
compounds
that
recurrently
in
high
demand
for
synthesis
and
use
various
fields
chemistry
biology.
We
report
the
first
Co(II)
catalyzed
one-component
one-pot
sustainable
acyl
only
from
hydrazides
under
mild
reaction
conditions.
Traditional
contemporary
methodologies
two
components
(usually
aldehydes/ketones/alcohols/styrene)
as
coupling
partners.
Our
protocol,
on
other
hand,
involves
situ
generation
aldehyde
intermediate
(detected
by
gas
chromatography)
hydrazide,
which
then
undergoes
condensation
with
another
molecule
same
hydrazide
pot
to
yield
presence
base
K2
CO3
low-cost
Co(OAc)2
⋅
4H2
O
catalyst.
This
method
shows
good
functional
group
tolerance
excellent
products.
Furthermore,
some
resulting
have
been
used
synthetic
precursors
explored
post-synthetic
modifications
afford
N-heterocyclic
compounds.
photoswitchable
properties
few
synthesized
also
using
their
E/Z
isomerization
around
C=N
bond,
realized
high-pressure
liquid
chromatography
(HPLC)
UV-vis
spectroscopic
studies.
Inorganic Chemistry,
Год журнала:
2023,
Номер
62(44), С. 18198 - 18208
Опубликована: Окт. 23, 2023
A
series
of
cyclometalated
C,N-chelate
half-sandwich
ruthenium
complexes
based
on
N-heterocyclic
ligands
were
prepared
through
a
simple
route
with
good
yields.
These
air-
and
moisture-stable
showed
excellent
catalytic
efficiency
in
phenoxy
carbonylation
aryl
halides
phenyl
formate
derivatives
as
CO
source
phenol
coupling
partner
under
air.
Ester
products
obtained
high
yields
at
room
temperature
without
the
need
for
an
inert
atmosphere.
The
activity,
broad
substrate
range,
mild
reaction
conditions
made
this
system
potential
industrial
production.
In
addition,
DFT
study
has
been
carried
out
to
elaborate
possible
mechanism
Ru-catalyzed
reaction.
Applied Organometallic Chemistry,
Год журнала:
2024,
Номер
38(8)
Опубликована: Май 30, 2024
A
highly
efficient
carbonylation
of
aryl
halides
using
half‐sandwich
iridium
catalysis
was
developed,
providing
a
new
avenue
for
synthesizing
carboxylic
ester
derivatives
and
yielding
consistently
impressive
results.
These
complexes
demonstrated
remarkable
catalytic
performance
in
the
coupling
reaction
phenyl
formate
as
source
CO,
phenol,
starting
material
presence
air
possessed
good
moisture
stability
properties.
Ester
products
with
different
substituents
were
synthesized
at
low
temperatures
without
need
an
inert
atmosphere,
leading
to
high
yields.
The
broad
substrate
scope,
activity,
mild
conditions
suggest
promising
industrial
applications
this
system.
desired
metal
1
–
4
have
been
well
proven
by
attenuated
total
reflectance‐Fourier
transform
infrared
(ATR‐FTIR),
nuclear
magnetic
resonance
(NMR),
elemental
analysis
(EA).
molecular
structure
cyclometalated
2
3
through
X‐ray
crystallography.
Additionally,
possible
mechanism
Ir‐catalyzed
process
is
further
supported
density
functional
theory
(DFT)
study.
Chemistry - An Asian Journal,
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 12, 2024
Abstract
Herein,
we
have
reported
a
new
series
of
NNS‐donor
ligands
coordinated
Ni(II)
complexes
and
utilized
them
as
catalytic
activator
to
synthesize
N
‐alkylated
amines
1,2‐disubstituted
benzimidazoles.
The
reaction
thiophenol/4‐chlorothiophenol/4‐methylthiophenol/4‐methoxythiophenol
with
2‐bromo‐
‐quinolin‐8‐yl‐acetamide
in
presence
sodium
hydroxide
ethanol
at
80
°C
gave
[C
9
H
6
N‐NH−C(O)−CH
2
‐S−Ar]
[Ar=C
5
(
L1
);
C
4
Cl‐4
(L2
Me‐4
(L3
)
‐OMe‐4
(L4
)],
respectively.
corresponding
‐
L4
Ni(OAc)
methanol
for
3
hours
resulted
octahedral
nickel
[(
‐H)
Ni]
C1
),
L2
C2
L3
C3
C4
All
compounds
been
characterized
by
micro
spectroscopic
analysis.
molecular
structure
–
has
also
determined
single
crystal
X‐ray
diffraction
data.
utility
were
evaluated
the
‐alkylation
aniline
benzyl
alcohols,
benzimidazoles
synthesis.
obtained
results
indicate
that
complex
showed
better
activity
both
alcohols
[catalyst
loading:
2.0
mol
%;
Yield
up
92
%],
derivatives
94
%)].
mechanistic
studies
suggested
works
through
hydrogen
borrowing
from
alcohol
its
subsequent
utilization
situ
reduction
imine.
experimentally
observed
reactivity
patterns
found
good
agreement
HOMO‐LUMO
energy
gaps
DFT
analysis
complexes.
Applied Organometallic Chemistry,
Год журнала:
2024,
Номер
38(11)
Опубликована: Июль 25, 2024
A
series
of
N
,
‐chelate
half‐sandwich
iridium
complexes
were
synthesized
by
a
simple
method
with
good
yields.
The
dehydrogenation
aromatic
and
aliphatic
primary
alcohols
to
corresponding
carboxylic
acids
has
been
successfully
achieved
the
prepared
air
stable
under
mild
reaction
conditions.
Carboxylic
obtained
in
high
yields
open
flask
condition
broad
substrates
tolerance
sensitive
functional
groups.
Such
catalyst
system
showed
desirable
stability
catalytic
activity,
achievement
TOF
372.0
h
−1
could
be
observed
an
extremely
low
loading
only
0.05
mol%.
Furthermore,
sustainable
reused
for
minimum
five
cycles
without
obviously
losing
its
highlighting
potential
application
industry.
Structure
1
3
determined
single‐crystal
X‐ray
analysis.