l-Aspartic acid-functionalized magnetic nanoparticles: as a new magnetically reusable bifunctional acid–base catalysts for the synthesis of benzo[b]pyran and pyrano[3,2–c] chromene derivatives
Scientific Reports,
Год журнала:
2025,
Номер
15(1)
Опубликована: Янв. 2, 2025
Язык: Английский
DABCO dicationic ionic solid supported polymer (DDIS@PS) mediated synthesis of diverse 2-amino-4H-chromenes and xanthenes: a cascade Knoevenagel–Michael approach
New Journal of Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
This
work
documented
the
synthesis
of
diverse
bioactive
polysubstituted
2-amino-4
H
-chromenes
using
a
DABCO
dicationic
ionic
solid
(DDIS)
supported
on
Merrifield
resin
(DDIS@PS)
as
catalyst.
Язык: Английский
Solid‐state Suzuki–Miyaura cross‐coupling: A sustainable approach by DDIL‐stabilized magnetic separable and recyclable Pd nanoparticles with total solvent bypass
Applied Organometallic Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Июнь 9, 2024
A
new
method
for
the
sustainable
synthesis
of
various
functionalized
biaryls
through
solid‐state
Suzuki–Miyaura
cross‐coupling
reaction
has
been
developed.
This
protocol
employs
a
palladium
catalyst
anchored
on
diazabicyclo[2.2.2]octane
silica
ferrite
composite
(Pd‐DDIL@Fe
3
O
4
‐SiO
2
).
The
fully
characterized
using
multiple
techniques
such
as
FTIR,
XRD,
FESEM,
EDS,
elemental
mapping,
HR‐TEM,
XPS,
BET,
TGA‐DTA,
and
VSM.
Pd‐DDIL@Fe
surface
area
60.17
m
g
−1
magnetization
saturation
40.95
emu
.
TEM
analysis
revealed
rough
spherical
morphology
PdNPs
having
particle
size
7
nm.
excellent
activity
selectivity
towards
both
symmetrical
unsymmetrical
under
solid‐state,
solvent‐free
grinding
conditions
mortar
pestle.
is
eco‐friendly,
it
performed
at
room
temperature
without
any
solvents.
yield
products
(90–96%)
in
short
time
(3–20
min).
desired
are
isolated
easily
use
organic
can
be
separated
an
external
magnet
reused
least
six
times
with
admirable
change
yield.
Additionally,
catalytic
system
shown
to
have
high
TON
TOF,
thus
confirming
its
sustainability.
Язык: Английский
Silica-Supported Bi2O3-Cr2O3 Nanocomposite: Efficient Catalyst for Pyrano[3,2-c]chromenes Synthesis and DFT Studies
Journal of Molecular Structure,
Год журнала:
2024,
Номер
1319, С. 139624 - 139624
Опубликована: Авг. 13, 2024
Язык: Английский
Pd(OAc)2/[C18–DABCO–C18]2Br: a nano palladium catalytic approach for Mizoroki–Heck and Suzuki–Miyaura coupling reactions in water
New Journal of Chemistry,
Год журнала:
2023,
Номер
47(43), С. 20171 - 20181
Опубликована: Янв. 1, 2023
In
this
study,
we
have
successfully
used
a
new
catalytic
system
comprised
of
Pd(OAc)
2
and
[C
18
–DABCO–C
]2Br
(at
ratio
1
:
10
mol%)
for
various
types
C–C
coupling
reactions,
including
Mizoroki–Heck
Suzuki–Miyaura,
in
water-based
medium.
Язык: Английский
In Situ generated PdNPs immobilized on Polystyrene Supported DABCO Dicationic Ionic Liquid: An Efficient and Reusable Catalyst for Suzuki and Heck Coupling Reactions
Journal of Organometallic Chemistry,
Год журнала:
2024,
Номер
unknown, С. 123390 - 123390
Опубликована: Сен. 1, 2024
Язык: Английский
ZrO2 Supported Cu Nanoparticles for Sonogashira and Ullmann Coupling Reactions Under Palladium-Free Conditions
Catalysis Letters,
Год журнала:
2023,
Номер
154(6), С. 3078 - 3090
Опубликована: Дек. 14, 2023
Язык: Английский
Brønsted Acid Saponin Combined Catalyst (BASapC) for the Synthesis of Diverse 1,1‐Dihomoarylmethane Scaffolds in Aqueous Solution
ChemistrySelect,
Год журнала:
2024,
Номер
9(42)
Опубликована: Ноя. 1, 2024
Abstract
The
present
study
describes
the
synthesis
of
various
bioactive
compounds,
including
bis‐coumarins,
bis‐lawsones,
bis‐dimedones,
and
bis‐indolylmethanes,
using
a
novel
catalytic
system
called
“Brønsted
acid
saponin
combined
catalyst”
(BASapC).
BASapC
was
formed
by
combining
p
‐toluenesulfonic
(PTSA)
in
an
aqueous
medium.
prepared
proved
to
be
effective
facilitating
cascade‐type
Knoevenagel–Michael
addition
reactions
between
aromatic
aldehydes
with
4‐hydroxycoumarin,
lawsone,
dimedone,
or
indole
at
80
°C.
In
system,
PTSA
acted
as
powerful
Brønsted
acid,
activating
reactants,
whereas
served
natural
surfactant,
enhancing
solubility
organic
compounds
water.
This
approach
established
straightforwardness
robustness
diversity‐oriented
(DoS),
delivering
desired
products
good
excellent
yields.
Additionally,
exhibited
recyclability
for
least
four
cycles
without
significant
loss
activity.
Язык: Английский
C18‐DABCO‐AA: A Novel Brønsted Acidic Gemini Surfactant for the Environmental Benign Synthesis of 2,3‑Dihydroquinazolin‑4(1H)‑ones in Water at Ambient Temperature
Vijaya S. Rajmane,
Sunita Shirke,
Omkar Sutar
и другие.
ChemistrySelect,
Год журнала:
2024,
Номер
9(43)
Опубликована: Ноя. 1, 2024
Abstract
We
have
successfully
synthesized
a
new
acidic
surfactant
named
C
18
‐DABCO‐AA,
which
contains
octadecyl
and
acetic
acid
substituent
on
DABCO
(1,4‐diazabicyclo
[2.2.2]
octane)
unit,
with
an
excellent
yield.
The
was
analyzed
using
FT‐IR,
1
H
NMR,
13
NMR
spectroscopic
techniques.
Its
thermal
behavior
by
the
TGA–DTA
technique.
Our
analysis
indicates
that
has
properties.
critical
micelle
concentration
(CMC)
is
0.80
mM
as
determined
conductivity
method
UV–vis
absorption
measurement
at
298.15
K.
Surfactant
also
showed
strong
properties
p
K
of
3.3.
It
best
catalyst
for
synthesis
2,3‑dihydroquinazolin‑4(1
)‐ones
(DHQs)
in
water
40
°C.
achieved
via
two‐component
reactions
various
aromatic
aldehydes
anthranilamide
CMC
‐DABCO‐AA.
extended
synthesizing
DHQs
different
ketones
under
similar
reaction
conditions.
products
were
yields
ranging
from
good
to
within
60–90
min.
Additionally,
aqueous
solution
‐DABCO‐AA
reused
up
five
times
minor
decrease
product
present
protocol
fast,
energy‐efficient,
can
be
used
large
scale
synthetic
purposes.
it
boasts
impressive
environmentally
friendly
credentials.
Язык: Английский