Exploring magnetically recoverable catalysts for the synthesis of benzoxazoles derivatives
Fadhel F. Sead,
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Jayanti Makasana,
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Shelesh krishna saraswat
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et al.
Applied Catalysis O Open,
Journal Year:
2025,
Volume and Issue:
unknown, P. 207031 - 207031
Published: Feb. 1, 2025
Language: Английский
Design, Synthesis, and Biological Evaluation of Benzo[d]oxazole-2-thio and Oxazolo[4,5-b]pyridine-2-thio Derivatives: Molecular Docking, POM Analysis, In Silico Pharmacokinetics, and Pharmacophore Insights for Antitumor, GPCR, and Kinase Targets
Pankaj B. Gour,
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Sumeer Ahmed,
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Ramalingam Gajendhiran
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et al.
Journal of Molecular Structure,
Journal Year:
2025,
Volume and Issue:
unknown, P. 141705 - 141705
Published: Feb. 1, 2025
Language: Английский
Anti-Cancer Activity and Molecular Docking of Some Benzoxazole Derivatives as Apoptosis Inducers in Non-Small Cell Lung Cancer
Burcu Baba,
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Çağla Zübeyde Köprü,
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İlkay Yıldız
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et al.
Published: Jan. 1, 2025
Language: Английский
A Sustainable Synthesis of Novel 2-(3,4-Disubstituted phenyl)benzoxazole Derivatives and Their Antiproliferative and Antibacterial Evaluation
Molecules,
Journal Year:
2025,
Volume and Issue:
30(8), P. 1767 - 1767
Published: April 15, 2025
This
study
describes
the
synthesis
of
O-alkylated
benzaldehydes
1–8,
Schiff
bases
9–28,
and
benzoxazole
derivatives
29–48
using
microwave,
ultrasound,
mechanochemical
reactions,
as
well
reactions
in
deep
eutectic
solvents
excellent
yields,
their
antiproliferative
antibacterial
activities.
The
vitro
evaluation
activity
for
newly
synthesised
against
a
diverse
panel
human
cancer
cell
lines,
such
LN-229,
Capan-1,
HCT-116,
NCI-H460,
DND-41,
HL-60,
K-562,
Z-138
demonstrated
that
majority
these
displayed
promising
anticancer
activity,
particularly
non-small
lung
(NSCLC)
cells
(NCI-H460).
Notably,
several
showed
enhanced
compared
to
included
reference
drug,
etoposide.
Considering
influence
substituents
at
position
5
ring
positions
3
4
phenyl
on
it
is
evident
41–48
bearing
methoxy
group
generally
exhibit
higher
compounds
29–40,
which
lack
substitution
3.
Furthermore,
substituted
with
morpholine
substituent,
those
an
N,N-diethyl
group,
exhibited
other
evaluated
derivatives.
Gram-positive
Gram-negative
bacteria
revealed
derivative
47
notable
bacterium
Pseudomonas
aeruginosa
(MIC
=
0.25
μg/mL)
Enterococcus
faecalis
0.5
μg/mL).
results
point
out
this
class
benzoxazoles
can
be
efficiently
synthesized
eco-friendly
methods
represent
candidates
further
design
optimization
aimed
developing
potent
agents.
Language: Английский
Green and Biogenic Synthesis of Cerium Oxide (CeO2) Nanoparticles: Heterogeneous Catalytic Synthesis of Isoxazol‐5(4H)‐one Derivatives and Assessment of Their Antibacterial Activity
Pranali Hadole,
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Sudip Mondal,
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Sampat Shingda
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et al.
ChemistrySelect,
Journal Year:
2025,
Volume and Issue:
10(18)
Published: May 1, 2025
Abstract
The
development
of
eco‐friendly,
sustainable,
and
efficient
catalytic
systems
has
become
a
highly
attractive
area
research
for
promoting
heterogeneous
organic
reactions.
In
this
study,
we
report
the
use
cerium
oxide
nanoparticles
(CeO₂
NPs)
as
catalyst
one‐pot
synthesis
isoxazol‐5(4H)‐one
derivatives.
CeO₂
NPs
were
synthesized
via
an
environmentally
benign
method
using
extract
from
Holy
Basil
(Ocimum
sanctum),
offering
green,
cost‐effective
approach.
This
green
not
only
minimizes
hazardous
chemicals
but
also
enhances
physiochemical
properties
NPs,
including
their
performance.
activity
was
evaluated
through
reactions
involving
variety
aldehydes,
hydroxylamine
hydrochloride,
β‐dicarbonyl
compounds.
A
wide
range
derivatives
obtained
with
excellent
yields
high
purity
under
mild
conditions.
Furthermore,
reusability
thoroughly
investigated,
demonstrating
minimal
loss
over
multiple
reaction
cycles.
study
highlights
promising
sustainable
synthesizing
valuable
heterocyclic
compounds
nanotechnology,
thereby
contributing
significantly
to
advancement
responsible
practices
in
synthetic
chemistry.
Moreover,
antibacterial
further
emphasize
significance
green‐synthesized
NPs.
Language: Английский