Results in Chemistry,
Год журнала:
2024,
Номер
7, С. 101538 - 101538
Опубликована: Янв. 1, 2024
Furocoumarins,
a
distinct
class
of
coumarins,
hold
diverse
therapeutic
potential
such
as
anti-inflammatory,
anticancer,
antiviral,
antidepressant,
and
more.
Focusing
on
the
past
seven
years,
review
highlights
transition
metal-free
synthesis
furo[3,2-c]coumarin
scaffolds.
Metal-free
responses
have
gained
popularity
because
growing
awareness
need
to
preserve
natural
resources
lessen
negative
effects
metal
usage
environment.
By
categorizing
techniques
into
two-component
reactions
MCRs,
provides
structured
understanding
these
synthetic
methodologies.
Abstract
1,4‐Naphthoquinones
(1,4‐NQs)
are
an
important
class
of
molecules
with
diverse
pharmaceutical
applications.
Lawsone,
a
naturally
occurring
molecule
range
bioactivities,
falls
in
the
1,4‐NQs.
It
possesses
1,3‐dicarbonyl
functionality,
which
has
been
utilized
synthesis
bis‐lawsones
reaction
aldehydes.
In
this
review
we
have
discussed
notable
developments
bis‐lawsone
from
2009
to
2023.
Also,
highlights
limitations
and
future
perspectives
area.
RSC Advances,
Год журнала:
2022,
Номер
12(20), С. 12843 - 12857
Опубликована: Янв. 1, 2022
A
highly
convenient
and
sustainable
one-pot
approach
for
the
diversely-oriented
synthesis
of
a
variety
medicinally
privileged
amino-substituted
4,8-dihydropyrano[3,2-
RSC Advances,
Год журнала:
2022,
Номер
12(22), С. 14022 - 14051
Опубликована: Янв. 1, 2022
Heterocycles
of
synthetic
and
natural
origin
are
a
well-established
class
compounds
representing
broad
range
organic
molecules
that
constitute
over
60%
drugs
agrochemicals
in
the
market
or
research
pipeline.
Considering
vast
abundance
these
structural
motifs,
development
chemical
processes
providing
easy
access
to
novel
complex
target
by
introducing
environmentally
benign
conditions
with
main
focus
on
improving
cost-effectiveness
transformation
is
highly
demanding
challenging.
Accordingly,
sonochemistry
appears
be
an
excellent
alternative
feasible
energy
input
has
recently
received
considerable
steadily
increasing
interest
synthesis.
However,
involvement
transition-metal-catalyst(s)
process
often
triggers
unintended
impact
greenness
sustainability
transformation.
Consequently,
enormous
efforts
have
been
devoted
developing
metal-free
routes
for
assembling
various
heterocycles
medicinal
interest,
particularly
under
ultrasound
irradiation.
The
present
review
article
aims
demonstrate
brief
overview
current
progress
accomplished
ultrasound-assisted
synthesis
pharmaceutically
relevant
diverse
using
transition-metal-free
catalysis.
Frontiers in Chemistry,
Год журнала:
2022,
Номер
10
Опубликована: Сен. 29, 2022
We
applied
the
Petasites
hybridus
rhizome
water
extract
as
green
media
so
that
Ag/Fe
3
O
4
/CdO@
multi-walled
carbon
nanotubes
magnetic
nanocomposites
(Ag/Fe
/CdO@MWCNTs
MNCs)
could
be
prepared.
also
evaluated
its
activity
by
using
in
one-pot
multicomponent
reaction
of
acetophenones,
diethyl
oxalate,
ammonium
acetate,
and
activated
carbonyl
compounds
such
ninhydrin,
isatin
acenaphthylene-1,2-dione,
malononitrile
hydrazoyl
chlorides
an
aqueous
medium
at
room
temperature
for
generation
spiro-1,2,4-triazines
new
derivatives
with
tremendous
output.
Moreover,
reducing
organic
pollutants
from
4-nitrophenol
(4-NP)
was
carried
out
generating
temperature.
The
results
displayed
reduced
a
short
time.
synthesized
have
NH
OH
functional
groups
having
acidic
hydrogen
high
antioxidant
power.
Also,
exhibited
antimicrobial
ability.
For
this
purpose,
disk
diffusion
method
two
kinds
bacteria,
Gram-positive
Gram-negative,
were
employed
analysis.
Furthermore,
we
theory-based
quantum
chemical
methods
order
to
better
understand
mechanism
density.
To
generate
spiro-1,2,4-triazines,
process
showed
many
properties
reactions
time,
products
good
yields,
simple
extraction
catalyst
mixture
reactions.
Organic & Biomolecular Chemistry,
Год журнала:
2023,
Номер
21(7), С. 1518 - 1530
Опубликована: Янв. 1, 2023
A
highly
efficient
pot,
atom,
and
step
economical
method
for
the
construction
of
pharmacologically
potent
structurally
functionalized
1,4-dihydropyridines,
quaternary
centered
C-3
spiro[indoline-3,4'-pyridines],
C-11
spiro[indeno[1,2-b]quinoxaline-11,4'-pyridines]
via
rose
bengal
photoredox
catalysis
under
blue
LED
irradiation
in
an
aqueous
medium
at
room
temperature
has
been
developed.
The
products
were
isolated
excellent
yields
within
a
short
reaction
time
variety
functional
groups
transition
metal-
ligand-free
energy-efficient
conditions
green
solvent
system
with
high
mass
efficiency
process
intensity,
which
are
key
advantages
current
work.
Arabian Journal of Chemistry,
Год журнала:
2021,
Номер
15(3), С. 103654 - 103654
Опубликована: Дек. 20, 2021
Given
the
importance
of
highly
reactive
nature
and
attractiveness
coumarins
as
a
precursor
natural
products
pharmacological
agents,
tremendous
efforts
have
been
dedicated
to
their
synthesis
in
last
decades.
Starting
from
Knoevenagel,
Perkin,
Kostanecki-Robinson,
Pechmann,
Reformansky,
Baylis
Hillman
reactions
several
new
one-pot
multicomponent,
sequential
tandem
devised.
After
emergence
non-conventional
energy
sources
like
microwaves
(MW)
ultrasound
irradiation,
field
organic
has
reached
an
outstanding
level
this
century
terms
synthetic
efficiency
well
green
chemistry
viewpoint.
Enlightened
by
this,
great
deal
attention
paid
bioactive
coumarin-heterocycles
employing
approach
vast
array
procedures
established.
Therefore,
time
investigation
is
required
for
biological
aspects
these
hybrid
molecules.
The
present
review
aims
highlight
current
progress
achieved
either
linked
or
fused
with
diverse
five-
six-membered
heterocycles
making
utilization
ultrasound-assisted
strategies
2014
date.
Besides
highlighting
development
field,
we
attempted
point
out
drawbacks
challenges
associated
reaction
discovery,
which
would
hopefully
provide
impetus
future
exploration.
Scientific Reports,
Год журнала:
2023,
Номер
13(1)
Опубликована: Янв. 25, 2023
Here,
we
have
demonstrated
a
metal-free
energy-efficient
mechanochemical
approach
for
expedient
access
to
diverse
set
of
2-amino-3-cyano-aryl/heteroaryl-4H-chromenes,
tetrahydrospiro[chromene-3,4'-indoline],
2,2'-aryl/heteroarylmethylene-bis(3-hydroxy-5,5-dimethylcyclohex-2-enone)
as
well
tetrahydro-1H-xanthen-1-one
by
employing
the
reactivity
5,5-dimethylcyclohexane-1,3-dione/cyclohexane-1,3-dione
with
TsOH⋅H2O
Brønsted
acid
catalyst
under
water-assisted
grinding
conditions
at
ambient
temperature.
The
ability
accomplish
multiple
C-C,
C=C,
C-O,
and
C-N
bonds
from
readily
available
starting
materials
via
domino
multicomponent
strategy
in
absence
metal-catalyst
volatile
organic
solvents
an
immediate
reduction
cost
transformation
without
necessitates
complex
operational
procedures,
features
significant
highlights
this
approach.
excellent
yield
products,
broad
functional
group
tolerances,
easy
set-up,
column-free,
scalable
synthesis
ultralow
loading,
short
reaction
time,
waste-free,
ligand-free,
toxic-free,
are
other
notable
advantages
greenness
sustainability
protocol
were
also
established
demonstrating
several
green
metrics
parameters.
RSC Advances,
Год журнала:
2023,
Номер
13(19), С. 13337 - 13353
Опубликована: Янв. 1, 2023
A
highly
promising
approach
for
the
synthesis
of
functionalized
1,1-dihomoarylmethane
scaffolds
(bis-dimedones,
bis-cyclohexanediones,
bis-pyrazoles,
and
bis-coumarins)
using
g-C3N4·SO3H
ionic
liquid
via
Knoevenagel-Michael
reaction
has
been
developed
synthesized
derivatives
were
well
characterized
spectral
studies.
The
method
involved
C-H
activated
acids
with
a
range
aromatic
aldehydes,
in
2
:
1
ratio
catalyzed
by
catalyst.
use
as
catalyst
several
benefits,
such
low
cost,
easy
preparation,
high
stability.
It
was
from
urea
powder
chloro-sulfonic
acid
thoroughly
FT-IR,
XRD,
SEM,
HRTEM.
present
work
unveils
environmentally
friendly
synthesizing
yield,
selectivity,
efficiency,
mild
conditions,
no
need
chromatographic
separation,
short
times.
adheres
to
green
chemistry
principles
offers
viable
alternative
previously
reported
methods.