Herein,
a
Mn
catalytic
protocol
has
been
developed
for
the
cycloalkene
ring
expansion
synthesis
of
azaheterocycles,
allowing
broad-substrate-scope
access
to
pyridine
and
isoquinoline
derivatives.
The
initial
monoaddition
an
azidyl
radical
alkene
further
as-generated
C-radical
addition
O
Abstract
Transition
metal‐catalyzed
cross‐coupling
reactions
have
become
a
powerful
and
widely
used
synthetic
approach
for
the
construction
of
both
carbon‐carbon
carbon‐heteroatom
bonds.
These
revolutionized
chemistry
by
enabling
efficient
formation
complex
molecular
architectures.
Among
various
methods
available,
bimolecular
homolytic
substitution
(S
H
2)
reaction
has
emerged
as
an
attractive
versatile
method
C(sp
3
)−C(sp
)
)‐heteroatom
In
recent
years,
significant
progress
been
made
in
development
radical
S
2
reactions,
particularly
those
involving
different
transition
metal
complexes
such
cobalt,
nickel,
iron.
advancements
expanded
scope
allowing
greater
diversity
substrate
compatibility
conditions.
this
review,
we
aim
to
highlight
latest
breakthroughs
mechanistic
insights
into
focusing
on
role
catalysts
facilitating
these
transformations.
We
will
discuss
types
that
employed,
pathways
involved,
potential
applications
synthesis
organic
molecules.
Abstract
Organoboron
compounds
are
recognized
as
essential
synthetic
intermediates
in
organic
chemistry
and
have
found
broad
applications
pharmaceutical
materials
science.
In
recent
years,
the
development
of
novel
boronating
reagents
has
opened
new
avenues
for
synthesis
organoboron
compounds.
Among
these,
N-heterocyclic
carbene
boranes
(NHC-boranes),
with
their
unique
advantages,
garnered
sustained
interest
evolved
into
important
precursors
boron-centered
radicals,
participating
a
diverse
array
visible-light-induced
borylation
reactions.
This
short
review
primarily
focuses
on
radical
reactions
involving
NHC-boranes,
summarizing
latest
advancements
field
offering
inspiration
subsequent
research.
1
Introduction
2
Photoinduced
Borylation
via
NHC-Boryl
Radicals
2.1
Polyfluoroarenes
2.2
Arenes
2.3
Alkenes
2.4
Alkynes
2.5
Other
Substrates
3
Conclusion
Future
Prospects
Herein,
a
Mn
catalytic
protocol
has
been
developed
for
the
cycloalkene
ring
expansion
synthesis
of
azaheterocycles,
allowing
broad-substrate-scope
access
to
pyridine
and
isoquinoline
derivatives.
The
initial
monoaddition
an
azidyl
radical
alkene
further
as-generated
C-radical
addition
O