Visible-light induced direct C(sp3)–H functionalization: recent advances and future prospects
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(18), P. 5278 - 5305
Published: Jan. 1, 2024
This
review
summarizes
the
latest
methodological
advances
in
photocatalytic
C(sp
3
)–H
functionalization,
with
a
particular
emphasis
on
formation
of
C–P,
C–B,
C–S
bonds,
etc
.,
and
some
prominent
efforts
asymmetric
C–H
functionalization.
Language: Английский
Unleashing the potentiality of metals: synergistic catalysis with light and electricity
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(14), P. 4024 - 4040
Published: Jan. 1, 2024
This
review
provides
a
comprehensive
overview
of
metal
catalysis
in
photo-electrochemical
systems,
discussing
reaction
mechanisms
and
offering
prospects
for
this
triadic
catalytic
mode.
Language: Английский
Towards a more Sustainable Photocatalysis using Copper and Iron
Current Opinion in Green and Sustainable Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100998 - 100998
Published: Jan. 1, 2025
Language: Английский
C(sp<sup>3</sup>)‐H Functionalization Using Chlorine Radicals
Advanced Synthesis & Catalysis,
Journal Year:
2024,
Volume and Issue:
366(13), P. 2898 - 2918
Published: May 18, 2024
Abstract
Converting
any
desired
C−H
bond
to
the
intended
C−Z
in
a
given
organic
molecule
could
be
final
peak
of
functionalization
methodology.
Among
three
types
bonds,
ubiquitous
C(
sp
3
)−H
has
gained
particular
attention,
especially
last
two
decades.
There
are
different
ways
transform
bonds
into
bonds.
The
use
chlorine
radicals
is
one
these
methods
with
promising
future.
literature
review
shows
that
sources
have
been
used
for
chlorine,
including
chloride
ions
(HCl
or
salts),
coordinated
chlorides
(transition
metal
complexes),
and
(organochlorine
compounds).
However,
HCl
FeCl
most
attention
among
sources.
major
convert
from
radicals:
1)
oxidation
hydrogen
salts,
2)
photolysis
chloride,
3)
transition
insertion
C−Cl
This
summarizes
published
research
papers
on
functionalization.
Therefore,
chlorination
reactions
which
do
not
play
direct
role
cleavage
within
scope
this
review.
Language: Английский
Construction of C–P Bonds from Free Cyclobutanone Oximes and Chlorophosphines via Radical–Radical Coupling
Lulu Yang,
No information about this author
Jiale Wu,
No information about this author
Yang Li
No information about this author
et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(15), P. 3208 - 3212
Published: April 10, 2024
Herein,
we
report
a
catalyst-free
reaction
of
cyclobutanone
oximes
with
chlorophosphines
(R2PCl),
which
forms
fragile
C═N–O–PR2
species
that
undergoes
N–O
homolysis,
fragmentation,
and
radical–radical
coupling,
leading
to
the
formation
cyano-containing
phosphine
oxides
in
good
yields.
The
features
an
situ
activation
for
radical
generation,
R2PCl
plays
dual
role
as
both
activator
reactant.
Language: Английский
Iron Photoredox Catalysis as an Effective Tool for Organic Synthesis via Visible‐Light‐Induced Homolysis (VLIH)
ChemistrySelect,
Journal Year:
2025,
Volume and Issue:
10(4)
Published: Jan. 1, 2025
Abstract
Owing
to
its
possible
advantages
for
the
environment
and
economy,
photoredox
catalysis
of
organic
processes
fueled
by
iron
has
garnered
a
lot
interest
recently.
The
potential
photo‐induced
single‐electron
transfer
(SET)
events
occurring
outside
sphere
is
now
well
acknowledged.
Currently,
focus
shifted
newly
discovered
photoactivation
method
that
based
on
an
inner‐sphere
mode
reactivity
caused
population
visible‐light‐induced
homolysis
(VLIH)
states.
VLIH
activation,
in
contrast
photoredox,
specific
complexes,
offers
distinct
profiles,
does
not
require
redox
potentials
coincide.
These
attractive
properties
have
prompted
development
strategies
use
this
blueprint
manufacture
highly
reactive
open‐shell
species
mild
environments.
purpose
contribution
promote
novel
synthetic
techniques
sustainable
chemical
transformations
offer
educational
instrument
understanding
evolving
idea.
Language: Английский
Iron-Catalyzed Multicomponent C–H Alkylation of in Situ Generated Imines via Photoinduced Ligand-to-Metal Charge Transfer
Pengcheng Li,
No information about this author
Jia‐Lin Tu,
No information about this author
Ao-Men Hu
No information about this author
et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(30), P. 6347 - 6352
Published: July 22, 2024
Herein,
we
describe
a
novel
photoinduced
iron-catalyzed
strategy
for
multicomponent
C-H
alkylation
of
in
situ
generated
imines.
By
utilizing
the
alkyl
radicals
through
iron-mediated
photocatalytic
activation,
imines
formed
are
further
subjected
to
addition
reactions,
resulting
synthesis
various
secondary
and
tertiary
amine
products.
This
method
is
simple
operate
does
not
require
additional
oxidants.
It
applicable
inert
alkane
substrates
such
as
cyclic
alkanes,
ethers,
toluene,
ketones.
The
reaction
also
compatible
with
aromatic
amines,
halogenated
well
aldehydes,
cinnamaldehyde,
among
other
different
types
aldehydes.
Language: Английский
Recent Progress in Metal-Catalyzed C(sp³)-P Bond Formation
Tetrahedron,
Journal Year:
2024,
Volume and Issue:
168, P. 134352 - 134352
Published: Nov. 1, 2024
Language: Английский
Photoinduced Ligand-to-Metal Charge Transfer (LMCT) in Organic Synthesis: Reaction Modes and Research Advances
Chemical Communications,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 20, 2024
In
recent
years,
visible
light-induced
ligand-to-metal
charge
transfer
(LMCT)
has
emerged
as
an
attractive
approach
for
synthesizing
a
range
of
functionalized
molecules.
Compared
to
conventional
photoredox
reactions,
photoinduced
LMCT
activation
does
not
depend
on
redox
potential
and
offers
diverse
reaction
pathways,
making
it
particularly
suitable
the
inert
bonds
functional
modification
complex
organic
This
review
highlights
indispensable
role
in
synthetic
chemistry,
with
focus
advancements
LMCT-mediated
hydrogen
atom
(HAT),
C-C
bond
cleavage,
decarboxylative
transformations,
radical
ligand
(RLT)
reactions.
Language: Английский