Organic Chemistry Frontiers,
Journal Year:
2022,
Volume and Issue:
10(3), P. 668 - 674
Published: Dec. 19, 2022
A
one-pot
stepwise
strategy
has
been
developed
to
afford
C3-heteroaryl
3-fluorooxindoles
via
a
Ce(
iii
)/photoassisted
cross-dehydrogenative
coupling/fluorooxidation
process
in
moderate-to-good
yields
with
excellent
functional
group
compatibility.
Organic Chemistry Frontiers,
Journal Year:
2022,
Volume and Issue:
9(13), P. 3598 - 3623
Published: Jan. 1, 2022
The
combination
of
visible
light
photoredox
catalysis
with
direct
difluoromethylation
has
allowed
the
synthesis
a
large
choice
CF
2
H-containing
value-added
molecules
under
very
mild
reaction
conditions.
European Journal of Organic Chemistry,
Journal Year:
2023,
Volume and Issue:
unknown
Published: Sept. 11, 2023
Abstract
The
multicomponent
reactions
of
quinoxalin‐2(1
H
)‐ones
has
attracted
considerable
interest
due
to
their
significant
biological
and
chemical
activities.
very
recent
advances
(from
2021
the
beginning
2023)
on
radical
three‐component
cascade
reaction
)‐one
derivatives
at
C3
position
were
summarized
in
this
mini‐review.
According
kind
types
involved,
some
representative
examples
detailed
mechanism
have
been
categorized
discussed.
red
front
was
covered
by
Figure
1.
The Chemical Record,
Journal Year:
2023,
Volume and Issue:
23(9)
Published: May 22, 2023
Abstract
In
the
last
few
years,
many
reagents
and
protocols
have
been
developed
to
allow
for
efficient
fluorofunctionalization
of
a
diverse
set
scaffolds
ranging
from
alkanes,
alkenes,
alkynes,
(hetero)arenes.
The
concomitant
rise
organofluorine
chemistry
visible
light‐mediated
synthesis
synergistically
expanded
fields
mutually
benefitted
developments
in
both
fields.
this
context,
light
driven
formations
radicals
containing
fluorine
major
focus
discovery
new
bioactive
compounds.
This
review
details
recent
advances
progress
made
fluoroalkylation
heteroatom
centered
radical
generation.
ACS Catalysis,
Journal Year:
2024,
Volume and Issue:
14(18), P. 13557 - 13566
Published: Aug. 28, 2024
The
incorporation
of
the
difluoromethyl
(CF2H)
group
into
arenes
has
increasingly
been
recognized
as
important
in
drug
discovery.
Herein,
we
report
a
divergent
cross-coupling
method
for
constructing
both
aryl
difluoromethanes
and
difluoroketones
from
thianthrenium
salts.
Site
selectivity
Negishi-type
coupling
C1
insertion
reactions
was
achieved
under
palladium
catalysis.
Both
transformations
proceed
with
broad
functional
tolerance,
enabling
late-stage
difluoromethylation
difluoromethylcarbonylation
complex
molecules.
synthetic
utility
this
demonstrated
by
synthesizing
four
pharmaceutical
analogues
same
precursor
applying
it
downstream
functionalization
difluoroketones.
Organic Chemistry Frontiers,
Journal Year:
2022,
Volume and Issue:
9(15), P. 4192 - 4208
Published: Jan. 1, 2022
In
this
review,
we
summarize
the
state-of-the-art
advances
in
difluoromethylation
of
heterocycles
via
a
radical
process
over
past
few
years
(2018
to
early
2022).
Organic Chemistry Frontiers,
Journal Year:
2023,
Volume and Issue:
11(3), P. 954 - 1014
Published: Dec. 14, 2023
The
review
summarises
various
photo-
and
electrochemical
strategies
for
trifluoromethylation
fluoroalkylation
of
different
C(sp
3
)–H,
2
C(sp)–H
bonds
in
several
classes
organic
molecules.
Chemical Communications,
Journal Year:
2024,
Volume and Issue:
60(49), P. 6268 - 6271
Published: Jan. 1, 2024
An
organophotoredox-catalyzed
direct
Csp
3
–H
alkylation
of
3,4-dihydroquinoxalin-2-ones
employing
N
-(acyloxy)phthalimides
to
provide
corresponding
products
in
good
yields
is
described.