Organic & Biomolecular Chemistry,
Год журнала:
2022,
Номер
20(25), С. 5104 - 5114
Опубликована: Янв. 1, 2022
An
Ag-catalysed
three-component
reaction
of
alkynyl
aryl
ketones
bearing
an
ortho
-methoxy
group,
element
selenium,
and
arylboronic
acid,
providing
a
facile
route
to
selenofunctionalized
chromone
products
has
been
investigated.
Organic & Biomolecular Chemistry,
Год журнала:
2021,
Номер
19(7), С. 1438 - 1458
Опубликована: Янв. 1, 2021
The
review
highlighted
diverse
annulations,
including
nitrogen,
oxygen,
sulfur
heterocycles
and
carbocylizations
via
Rh(iii)/Ir(iii)-catalyzed
C–H
functionalization/annulation
with
various
arene
carbene
precursors.
ChemCatChem,
Год журнала:
2019,
Номер
12(9), С. 2358 - 2384
Опубликована: Дек. 18, 2019
Abstract
Selective
functionalization
of
ubiquitous
C−H
bonds
molecules
would
provide
novel
retrosynthetic
insights
and
powerful
tools
for
the
rapid
construction
molecular
complexity.
In
this
context,
Cp*Ir(III)
complexes
have
exhibited
versatile
reactivity
towards
selective
conversion
bonds,
with
key
features
that
include
use
readily
transformable
raw
materials,
great
selectivity
(chemo‐,
stereo‐
regio‐),
high
efficiency,
mild
reaction
conditions
they
enable
late‐stage
modification
complex
molecules.
Recently,
catalysis
has
achieved
a
broad
range
reactions
such
as
multiple
dehydrogenations
stereoselective
C−X
bond
formations.
These
advancements
are
valuable
to
organometallic
chemists
efficient
synthesis
functionalized
architectures.
Organic Chemistry Frontiers,
Год журнала:
2020,
Номер
7(9), С. 1107 - 1112
Опубликована: Янв. 1, 2020
The
synthesis
of
C2-nitrogenated
chromones
has
been
performed
via
reactions
enaminones
and
nitrogen
nucleophiles
based
on
an
unconventional
β-C–H
bond
functionalization
a
featured
chromone
annulation
enaminones.
The Chemical Record,
Год журнала:
2021,
Номер
21(12), С. 4088 - 4122
Опубликована: Окт. 14, 2021
Abstract
The
past
decade
has
witnessed
tremendous
developments
in
transition‐metal‐catalyzed
C−H
bond
activation
and
subsequent
carbene
migratory
insertion
reactions,
thus
assisting
the
construction
of
diverse
arene/heteroarene
scaffolds.
Various
transition‐metal
catalysts
serve
this
purpose
provide
efficient
pathways
for
an
easy
access
to
substituted
heterocycles.
A
brief
introduction
metal‐carbenes
been
provided
along
with
key
mechanistic
underlying
coupling
reactions.
review
is
a
concise
knowledge
about
directing
group‐assisted
varied
arenes/heteroarenes
acceptor‐acceptor/donor‐acceptor
diazo
compounds.
also
highlights
synthesis
various
carbocycles
fused
heterocycles
through
pathways,
via
C−C,
C−N
C−O
forming
mechanism
usually
involves
process,
followed
by
leading
coupling.
Mini-Reviews in Medicinal Chemistry,
Год журнала:
2021,
Номер
22(7), С. 1030 - 1063
Опубликована: Ноя. 24, 2021
Chromones
are
the
class
of
secondary
metabolites
that
broadly
occur
in
plant
kingdom
a
noticeable
quantity.
This
rigid
bicyclic
system
has
been
categorized
"as
privileged
scaffolds
compounds"
medicinal
chemistry.
Their
wide
biological
responses
have
made
them
an
important
moiety
drug
discovery
program.
review
provides
updates
on
various
methods
synthesis
chromones
and
applications
Various
synthetic
strategies
for
construction
include
readily
available
phenols,
salicylic
acid
its
derivatives,
ynones,
chalcones,
enaminones,
2-hydroxyarylalkylketones
as
starting
materials.
Synthesis
by
using
metal,
metal-free,
nanomaterials
different
other
catalysts
is
herein
included.
Details
diverse
activities
chromone
derviatives,
such
anti-cancer,
antimicrobial,
anti-viral,
anti-inflammatory,
antioxidant,
Monoamine
Oxidase-B
(MAO-B)
inhibitors,
anti-
Alzheimer's
agents,
anti-diabetic
having
antihistaminic
potential,
acting
antiplatelet
discussed.
The Journal of Organic Chemistry,
Год журнала:
2023,
Номер
88(6), С. 4017 - 4023
Опубликована: Март 2, 2023
A
facile
cascade
reaction
for
the
site
selective
synthesis
of
2-cyanochromones
is
described.
By
using
simple
o-hydroxyphenyl
enaminones
and
potassium
ferrocyanide
trihydrate
(K4[Fe(CN)6]3·3H2O)
as
starting
materials
I2/AlCl3
promoters,
products
are
furnished
via
tandem
chromone
ring
formation
C–H
cyanation.
The
in
situ
3-iodochromone
a
formal
1,2-hydrogen
atom
transfer
(HAT)
process
account
unconventional
selectivity.
In
addition,
2-cyanoquinolin-4-one
has
been
realized
by
employing
corresponding
2-aminophenyl
enaminone
substrate.
ACS Central Science,
Год журнала:
2021,
Номер
7(5), С. 739 - 747
Опубликована: Апрель 21, 2021
There
is
a
growing
awareness
of
the
underlying
power
catalytic
reactions
in
water
that
not
limited
to
innate
sustainability
alone.
Some
Type
III
are
catalytically
accelerated
without
dissolution
reactants
and
occasionally
highly
selective,
as
shown
by
comparison
with
corresponding
run
organic
solvents
or
under
solvent-free
conditions.
Such
catalysts
diversified,
including
hydrophilic,
lipophilic,
even
solid
catalysts.
In
this
Outlook,
we
highlight
impressive
characteristics
illustrative
catalysis
exerted
despite
immiscibility
substrates
reveal
intrinsic
benefits
these
enigmatic
for
synthetic
chemistry,
albeit
many
details
remaining
unclear.
We
hope
brief
introduction
expanding
field
"aquachemistry"
will
inspire
chemists
use
platform
invent
new
transformations.
Green Chemistry,
Год журнала:
2022,
Номер
24(6), С. 2296 - 2320
Опубликована: Янв. 1, 2022
This
tutorial
review
gathers
landmark
work
on
transition-metal
mediated
C–H
activation
reactions
using
more
sustainable
approaches.
We
endeavour
to
promote
and
propagate
such
lines
of
research,
reducing
the
usage
hazardous
synthetic
routes
in
chemical
synthesis.
Chemical Communications,
Год журнала:
2022,
Номер
58(57), С. 7850 - 7873
Опубликована: Янв. 1, 2022
Olefins
and
akynes
are
synthetically
important
building
blocks
in
modern
organic
synthesis.
This
review
highlights
the
recent
developments
direct
functionalization
of
olefins
alkynes
via
photoinduced
copper-based
catalysis.