Organic & Biomolecular Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 3, 2024
Herein,
we
demonstrate
the
first
employment
of
(
E
)-alkylidine
benzofuran-2-one
for
high
enantio-
and
diastereoselective
construction
trifluormethylated
spiro[benzofuran-pyrrolidine]indolinedione.
Scientific Reports,
Год журнала:
2025,
Номер
15(1)
Опубликована: Янв. 22, 2025
Abstract
In
this
research,
graphene
oxide-polyaniline
(GO-PANI)
nanocomposite
was
successfully
synthesized
and
its
catalytic
performance
evaluated
for
the
synthesis
of
N-aryl-1,4-dihydropyridine
(1,4-DHP)
hydroquinoline
derivatives.
The
GO
nanosheets
were
prepared
using
Hummers’
method,
in-situ
polymerization
aniline
conducted
with
ammonium
persulfate
(APS)
serving
as
initiator.
demonstrated
notable
efficiency,
achieving
yields
80–94%
1,4-DHP
derivatives
84–96%
GO-PANI
thoroughly
characterized
by
various
techniques,
including
Fourier
Transforms
Infrared
spectroscopy
(FT-IR),
Field
Emission
Scanning
Electron
Microscopy
(FE-SEM),
X-ray
Diffraction
analysis
(XRD),
Thermogravimetric
(TGA),
Energy
Dispersive
(EDS),
all
which
confirmed
successful
nanocomposite.
Furthermore,
after
ten
cycles
reusability
testing,
retained
high
no
significant
degradation.
This
findings
indicate
that
is
a
promising
non-metal
catalyst
RSC Advances,
Год журнала:
2023,
Номер
13(11), С. 7063 - 7075
Опубликована: Янв. 1, 2023
Recent
updates
on
the
synthesis
of
CF
3
-containing
spirocyclic-oxindoles
by
employing
N
-2,2,2-trifluoroethylisatin
ketimines
are
described
in
this
review
article.
New Journal of Chemistry,
Год журнала:
2025,
Номер
49(6), С. 2418 - 2431
Опубликована: Янв. 1, 2025
This
study
presents
the
development
of
a
novel
organo-inorganic
hybrid
material
(zeolite-SO
3
H)
through
three-component
reaction
carbon
disulfide
and
1,3-propane
sultone
with
aminopropyl-functionalized
NaY
zeolite.
Abstract
We
present
the
first
application
of
olefinic
pyrazolone
in
conjunction
with
indole‐tethered
enal
an
aminocatalytic
remote
[4
+
2]
annulation
reaction,
successfully
yielding
tetrahydrocarbazole
spiropyrazolone
frameworks
moderate
to
good
yields,
accompanied
by
significant
enantio‐
and
diastereoselectivities.
The
robustness
this
developed
protocol
is
demonstrated
through
generation
a
diverse
array
22
examples,
all
exhibiting
consistent
yields
stereoselectivities.
Furthermore,
we
achieved
gram‐scale
synthesis
synthesized
biologically
relevant
fluorohexahydrofuranocarbazole
via
two‐pot,
three‐step
sequence
involving
2]‐addition,
reduction,
fluoroetherification
reactions.
Finally,
propose
plausible
mechanism,
supported
SC‐XRD
NOE
experiments,
highlighting
crucial
aspect
research.
Chemistry - An Asian Journal,
Год журнала:
2023,
Номер
18(14)
Опубликована: Май 22, 2023
After
the
emergence
of
organocatalysis,
field
asymmetric
synthesis
has
reached
an
exceptional
level
in
this
century.
Asymmetric
aminocatalysis,
among
other
organocatalytic
strategies,
proceeded
through
LUMO-lowering
iminium
ion
and
HOMO-raising
enamine
activation
appeared
as
a
powerful
synthetic
approach
for
realizing
potential
chiral
building
blocks
from
unmodified
carbonyl
compounds.
Consequently,
concept
strategy
plethora
transformations
based
on
enamine,
dienamine,
most
recently
trienamine,
tetraenamine,
pentaenamine
catalysis
been
devised.
In
mini-review
article,
we
disclosed
recent
progress
accomplished
aminocatalysis
polyenamine
strategies
functionalization
compounds,
covered
reports
2014
to
till
date.
Catalysis Science & Technology,
Год журнала:
2024,
Номер
14(9), С. 2619 - 2629
Опубликована: Янв. 1, 2024
The
synthesis
of
tetrahydropyridine
derivatives
under
visible-light
irradiation
using
a
photoactive
metal–organic
framework
and
the
evaluation
their
anti-tubercular
activities.