A
new
iron-catalyzed
three-component
perfluoroalkylarylation
of
styrenes
with
alkyl
halides
and
arenes
has
been
established.
Alkyl
undergo
halogen
atom
transfer
methyl
radicals
to
form
in
reactions
initiated
by
a
combination
Chemistry - A European Journal,
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 16, 2024
The
advancement
in
electrochemical
techniques
has
unlocked
a
new
path
for
achieving
unprecedented
oxidations
and
reductions
of
aryl
radical
precursors
controlled
selective
manner.
This
approach
facilitates
the
construction
aromatic
carbon-carbon
carbon-heteroatom
bonds.
In
light
green
merits
growing
importance
this
technique
chemistry,
review
aims
to
provide
an
overview
recent
advance
generation
radicals
organized
by
precursor
type,
with
focus
on
substrate
scope,
limitation,
underlying
mechanism,
thereby
inspiring
future
work
generation.
The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
89(5), С. 2885 - 2894
Опубликована: Фев. 14, 2024
Because
of
their
various
reactivities,
propargyl
acetates
are
refined
chemical
intermediates
that
extensively
applied
in
pharmaceutical
synthesis.
Currently,
reactions
between
and
chlorosilanes
may
be
the
most
effective
method
for
synthesizing
silylallenes.
Nevertheless,
owing
to
adaptability
selectivity
substrates,
transition
metal
catalysis
is
difficult
achieve.
Herein,
nickel-catalyzed
reductive
cross-coupling
substituted
vinyl
synthesis
tetrasubstituted
silylallenes
described.
Therein,
metallic
zinc
a
crucial
reductant
effectively
enables
two
electrophilic
reagents
selectively
construct
C(sp2)–Si
bonds.
Additionally,
Ni-catalyzed
mechanism
involving
radical
process
proposed
on
basis
deuteration-labeled
experiments.
The Chemical Record,
Год журнала:
2023,
Номер
23(11)
Опубликована: Июнь 12, 2023
Abstract
Harnessing
visible‐light
in
organic
synthesis
is
one
of
the
most
effective
methods
that
aligns
with
green
and
sustainable
chemistry
principles
hence
skyrocketed
last
two
decades.
Similarly,
three‐component
1,2‐dicarbofunctionalization
alkenes
alkynes
has
recently
been
a
great
choice
to
construct
complex
molecular
systems
an
easy
rapid
manner.
Therefore,
light‐induced
reactions
can
be
excellent
alternative
carry
out
reactions,
very
recently,
chemists
across
globe
have
fascinated
us
their
interesting
articles.
In
this
present
review,
we
summarized
recent
advancements
area
visible
light
induced
till
March
2023.
We
categorized
discussion
based
on
catalysts
used
transformations
for
better
understanding
different
important
aspects
these
also
covered.
The Chemical Record,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 3, 2025
Abstract
Owing
to
their
wide
utilizations
in
synthesis
and
products
prevalence
numerous
natural
products,
pharmaceuticals
functional
materials,
the
alkene
difunctionalization
methods
for
selective
transformations
of
olefins
are
important
have
attracted
much
attention
form
synthetic
chemists.
Among
them,
electrochemical
reaction
is
particularly
promising
has
becoming
a
potent
sustainable
tool
alkenes
into
vicinal
difunctionalized
structures
organic
through
simultaneous
incorporation
two
groups.
Herein,
we
summarize
recent
progress
reactions
according
types
as
well
category
radicals
over
past
five
years.
By
selecting
remarkable
examples,
elaborately
discussed
substrate
scope
mechanisms
olefin
reaction.
Chemical Reviews,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 7, 2025
Constructing
chemical
bonds
under
green
sustainable
conditions
has
drawn
attention
from
environmental
and
economic
perspectives.
The
dissociation
of
(hetero)aryl-halide
is
a
crucial
step
most
arylations
affording
(hetero)arene
derivatives.
Herein,
we
summarize
the
(hetero)aryl
halides
activation
enabling
direct
(hetero)arylation
trapping
reagents
construction
highly
functionalized
(hetero)arenes
benign
conditions.
strategies
for
aryl
iodides
are
classified
into
(a)
hypervalent
iodoarene
followed
by
functionalization
thermal/photochemical
conditions,
(b)
aryl-I
bond
in
presence
bases
with/without
organic
catalysts
promoters,
(c)
photoinduced
presence/absence
organophotocatalysts,
(d)
electrochemical
direct/indirect
electrolysis
mediated
organocatalysts
mediators
acting
as
electron
shuttles,
(e)
electrophotochemical
redox-active
organocatalysts.
These
modes
result
exhibiting
diverse
reactivity
formal
cations/radicals/anions
aryne
precursors.
coupling
these
reactive
intermediates
with
leads
to
facile
selective
formation
C-C
C-heteroatom
bonds.
ecofriendly,
inexpensive,
functional
group-tolerant
offer
alternatives
transition
metal-based
catalysis.
A
visible-light-mediated
photoredox
catalysis
for
β-C(sp3)–H
alkylation
of
1-(o-iodoaryl)alkan-1-ones
with
alkenes
via
1,5-hydrogen
atom
transfer
and
alkene
alkylarylation
to
produce
diverse
β-alkyl
arylalkanones
containing
a
quaternary
carbon
center
is
presented.
This
method
applicable
wide
range
activated
alkenes.
Mechanistic
studies
suggest
that
the
reaction
involves
radical
process.
Chinese Journal of Chemistry,
Год журнала:
2023,
Номер
42(6), С. 585 - 591
Опубликована: Ноя. 2, 2023
Comprehensive
Summary
A
straightforward
electrochemical
reduction
of
benzo[
b
]thiophene
1,1‐dioxides
with
HFIP
as
the
hydrogen
donor
has
been
reported
in
an
undivided
cell
under
metal‐free
conditions.
Moreover,
tolerance
various
functional
groups
and
scaled‐up
experiments
showed
practicability
potential
applications
this
methodology.
Organic Letters,
Год журнала:
2024,
Номер
26(29), С. 6114 - 6119
Опубликована: Июль 5, 2024
Difunctionalization
of
alkynes
has
gained
a
lot
interest
in
current
organic
chemistry.
Herein,
we
developed
an
electrophotocatalytic
multicomponent
cascade
reaction
and
indoles
with
sulfinic
acid
sodium
salts
using
elemental
tellurium
as
the
source.
Using
synergistic
anodic
oxidation
visible-light
irradiation,
various
β-(telluro)vinyl
sulfones
have
been
prepared.
This
strategy
features
mild
conditions,
excellent
substrate
scope,
readily
available
starting
materials,
great
functional
group
tolerance.
Organic Chemistry Frontiers,
Год журнала:
2024,
Номер
11(15), С. 4182 - 4186
Опубликована: Янв. 1, 2024
In
this
paper,
we
developed
an
electro-reductive
aryl-to-alkyl
radical
relay
arylation
reaction
of
a
remote
C(sp
3
)–H
bond
via
1,5-HAT
process.
This
protocol
features
mild
conditions,
simple
operation,
and
broad
substrate
scope.