Regio- and chemoselective synthesis of flavanone isosteres via multicomponent reactions: synergistic role of hydrogen bonding and solvent effects
Molecular Diversity,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 26, 2025
Язык: Английский
Sustainable Synthesis of Novel Tris‐thio/Semicarbazones and Tris‐rhodanines with Antiproliferative and Wastewater Treatment Applications
ChemistrySelect,
Год журнала:
2025,
Номер
10(19)
Опубликована: Май 1, 2025
Abstract
A
new
series
of
tris‐rhodanines
(
3
)
and
tris‐thio/semicarbazones
5
have
been
designed,
sono‐synthesized,
characterized
employing
diverse
spectral
methods.
Additionally,
the
copper
complex
6
derived
from
tris‐thiosemicarbazone
ligand
5b
successfully
photodegraded
methylene
blue
(MB)
showed
superior
effectiveness
(97%),
suggesting
its
potential
for
utilization
in
wastewater
treatment
systems.
Furthermore,
antiproliferative
activities
designed
compounds
evaluated
regarding
MCF‐7,
A549
(cancer
cell
lines),
MCF‐10A
(normal
lines).
The
results
indicated
that
developed
demonstrated
promising
inhibitory
impacts
(IC
50
=
1.27–11.57
µM),
even
outperforming
doxorubicin
certain
cases.
exhibited
noteworthy
anticancer
properties
<1.30
µM)
a
less
cytotoxic
influence
on
normal
line
85.07
as
leading
candidate
cancer‐preventing
medicaments.
structure‐activity
relationship
assessment
revealed
hydrogen
donor
motifs,
like
carboxyl
linked
to
rhodanine
or
terminal
benzyl
moiety
connected
tris‐thiosemicarbazones,
are
more
effective
activities.
density
functional
theory
(DFT)‐based
quantum
chemical
analysis
assembled
molecules
has
found
be
agreement
with
vitro
inhibiting
activity.
Lastly,
docking
evaluation
all
efficiently
interacted
targeted
proteins'
active
sites
(4AOR
6JZ0)
had
low
binding
energies,
particularly
5c
(−8.35,
−7.64
kcal/mol)
(−7.59,
−7.03
kcal/mol).
Язык: Английский
Hybrid Metal Catalysts as Valuable Tools in Organic Synthesis: An Overview of the Recent Advances in Asymmetric C─C Bond Formation Reactions
Molecules,
Год журнала:
2024,
Номер
29(21), С. 5090 - 5090
Опубликована: Окт. 28, 2024
Carbon–carbon
bond
formation
represents
a
key
reaction
in
organic
synthesis,
resulting
paramount
importance
for
constructing
the
carbon
backbone
of
molecules.
However,
traditional
metal-based
catalysis,
despite
its
advantages,
often
struggles
with
issues
related
to
efficiency,
selectivity,
and
sustainability.
On
other
hand,
while
biocatalysis
offers
superior
selectivity
due
an
extraordinary
recognition
process
substrate,
scope
applicable
reactions
remains
somewhat
limited.
In
this
context,
Artificial
Metalloenzymes
(ArMs)
Metallo
Peptides
(MPs)
offer
promising
not
fully
explored
solution,
merging
two
fields
transition
metal
catalysis
biotransformations,
by
inserting
catalytically
active
cofactor
into
customizable
protein
scaffold
or
coordinating
ion
directly
short
tunable
amino
acid
(Aa)
sequence,
respectively.
As
result,
these
hybrid
catalysts
have
gained
attention
as
valuable
tools
challenging
catalytic
transformations,
providing
systems
new-to-nature
properties
synthesis.
This
review
overview
recent
advances
development
ArMs
MPs,
focusing
on
their
application
asymmetric
carbon–carbon
bond-forming
reactions,
such
carbene
insertion,
Michael
additions,
Friedel–Crafts
cross-coupling
cyclopropanation,
underscoring
versatility
synthesizing
biologically
relevant
compounds.
Язык: Английский