A
green
and
practical
method
for
the
electrochemical
synthesis
of
tetrahydroimidazo[1,5-a]quinoxalin-4(5H)-ones
through
three-component
reaction
quinoxalin-2(1H)-ones,
N-arylglycines
paraformaldehyde
was
reported.
In
this
strategy,
EtOH
played
dual
roles
(eco-friendly
solvent
waste-free
pre-catalyst)
in
situ
generated
ethoxide
promoted
triple
sequential
deprotonations.
Organic & Biomolecular Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
This
review
highlights
the
recent
advances
in
multi-component
reactions
for
synthesizing
heterocyclic
compounds
via
green
approaches
including
photoredox
catalysis,
electrochemical
activation,
catalyst-free
methods
and
use
of
water
as
sole
solvent.
Frontiers in Chemistry,
Год журнала:
2022,
Номер
10
Опубликована: Окт. 10, 2022
Using
the
microwave-assisted
method,
novel
Fe3O4/Zn-metal
organic
framework
magnetic
nanostructures
were
synthesized.
The
crystallinity,
thermal
stability,
adsorption/desorption
isotherms,
morphology/size
distribution,
and
hysteresis
of
synthesized
characterized
by
XRD
patterns,
TGA
curve,
BET
technique,
SEM
image,
VSM
respectively.
After
confirming
nanostructures,
its
antimicrobial
properties
against
Gram-positive
bacterial,
Gram-negative
fungal
strains
based
on
minimum
inhibitory
concentration
(MIC),
bactericidal
(MBC),
fungicidal
(MFC)
values
studied.
MIC
in
activity
for
bacterial
strains,
between
16-128
μg/ml,
strain,
128
μg/ml
observed.
results
showed
that
high
specific
surface
area
caused
power
nanoparticles
to
be
high,
observed
effects
higher
than
some
known
commercial
drugs.
Another
advantage
was
catalytic
three-component
reaction
isatin,
malononitrile,
dimedone.
New
spiro
[indoline-pyranopyrimidines]
derivatives
with
efficiency.
that,
addition
recyclability,
could
less
time
previously
reported
methods.
investigating
range
10-20
min
an
efficiency
over
85%.
As
a
final
result,
it
can
concluded
microwave
synthesis
method
improves
unique
especially
area,
has
increased
Organic Letters,
Год журнала:
2023,
Номер
25(28), С. 5308 - 5313
Опубликована: Июль 7, 2023
Trifluoromethyl
bicyclo[1.1.1]pentanes
(BCPs)
have
attracted
significant
attention
from
the
scientific
community
and
pharmaceutical
industries
due
to
their
advantageous
physicochemical
properties
as
arene
bioisosteres.
Initial
photoredox
perfluoroalkylation
of
[1.1.1]propellane
triggers
tandem
reaction
perfluoroalkyl
BCP
radical
followed
by
Giese
addition
an
in
situ
generated
electron-deficient
alkene
Knoevenagel
condensation
a
four-component
fashion
form
1,3-functionalized
BCPs.
This
strategy
provides
easy
access
various
derivatives
with
added
advantage
nitrile
group
functional
handle
diversified
transformations.
methodology
offers
scalability
late-stage
derivatization
drug
molecules
high
chemoselectivity.
Angewandte Chemie International Edition,
Год журнала:
2023,
Номер
62(22)
Опубликована: Март 6, 2023
Radical
additions
onto
olefins
have
surfaced
as
an
increasingly
powerful
strategy
for
the
synthesis
of
difunctionalized
scaffolds.
However,
despite
major
advances,
known
approaches
continue
to
be
largely
limited
two
manifolds,
namely
1,2-difunctionalization
alkenes
and
remote
difunctionalization
via
hydrogen
atom
transfer
(HAT).
Herein,
we
describe
a
mechanistically
distinct
approach
by
photoinduced
carbon-carbon
(C-C)
activation/ring-opening
access
γ,δ-unsaturated
aldehydes
from
methylenecyclobutanols
sulfonyl
chlorides
strain
release.
Remarkably,
motif
on
products
was
easily
removed
another
photocatalytic
process,
which
enabled
concise
assembly
natural
product
alatanone
A.
The
synthetic
utility
our
reflected
versatile
functional
group
tolerance,
ample
substrate
scope,
scalability.
photocatalysis
represents
conceptually
alternative
existing
1,4-diversifications,
with
double
bond
remaining
in
thus
obtained
products.
A
green
and
practical
method
for
the
electrochemical
synthesis
of
tetrahydroimidazo[1,5-a]quinoxalin-4(5H)-ones
through
three-component
reaction
quinoxalin-2(1H)-ones,
N-arylglycines
paraformaldehyde
was
reported.
In
this
strategy,
EtOH
played
dual
roles
(eco-friendly
solvent
waste-free
pre-catalyst)
in
situ
generated
ethoxide
promoted
triple
sequential
deprotonations.