Chemical Society Reviews,
Год журнала:
2018,
Номер
47(15), С. 5786 - 5865
Опубликована: Янв. 1, 2018
This
review
provides
an
overview
of
the
use
electrochemistry
as
appealing
platform
for
expediting
carbon–hydrogen
functionalization
and
carbon–nitrogen
bond
formation.
Angewandte Chemie International Edition,
Год журнала:
2012,
Номер
51(36), С. 8960 - 9009
Опубликована: Авг. 6, 2012
Abstract
The
direct
functionalization
of
CH
bonds
in
organic
compounds
has
recently
emerged
as
a
powerful
and
ideal
method
for
the
formation
carbon–carbon
carbon–heteroatom
bonds.
This
Review
provides
an
overview
bond
strategies
rapid
synthesis
biologically
active
such
natural
products
pharmaceutical
targets.
Chemical Reviews,
Год журнала:
2016,
Номер
116(6), С. 3722 - 3811
Опубликована: Март 3, 2016
The
applications
of
copper
(Cu)
and
Cu-based
nanoparticles,
which
are
based
on
the
earth-abundant
inexpensive
metal,
have
generated
a
great
deal
interest
in
recent
years,
especially
field
catalysis.
possible
modification
chemical
physical
properties
these
nanoparticles
using
different
synthetic
strategies
conditions
and/or
via
postsynthetic
treatments
has
been
largely
responsible
for
rapid
growth
nanomaterials
their
In
addition,
design
development
novel
support
multimetallic
systems
(e.g.,
alloys,
etc.)
also
made
significant
contributions
to
field.
this
comprehensive
review,
we
report
approaches
Cu
(metallic
copper,
oxides,
hybrid
nanostructures)
immobilized
into
or
supported
various
materials
(SiO2,
magnetic
materials,
etc.),
along
with
synthesis
part
discusses
numerous
preparative
protocols
whereas
application
sections
describe
utility
as
catalysts,
including
electrocatalysis,
photocatalysis,
gas-phase
We
believe
critical
appraisal
will
provide
necessary
background
information
further
advance
nanostructured
Chemical Society Reviews,
Год журнала:
2011,
Номер
40(10), С. 5068 - 5068
Опубликована: Янв. 1, 2011
The
direct
functionalization
of
heterocyclic
compounds
has
emerged
as
one
the
most
important
topics
in
field
metal-catalyzed
C–H
bond
activation
due
to
fact
that
products
are
an
synthetic
motif
organic
synthesis,
pharmaceutical
industry,
and
materials
science.
This
critical
review
covers
recent
progresses
on
regioselective
dehydrogenative
coupling
reaction
heteroarenes,
including
arylation,
olefination,
alkynylation,
amination/amidation
mainly
utilizing
transition
metal
catalysts
(113
references).
Chemical Society Reviews,
Год журнала:
2012,
Номер
41(9), С. 3651 - 3651
Опубликована: Янв. 1, 2012
Rhodium(III)-catalyzed
direct
functionalization
of
C-H
bonds
under
oxidative
conditions
leading
to
C-C,
C-N,
and
C-O
bond
formation
is
reviewed.
Various
arene
substrates
bearing
nitrogen
oxygen
directing
groups
are
covered
in
their
coupling
with
unsaturated
partners
such
as
alkenes
alkynes.
The
facile
construction
C-E
(E
=
C,
N,
S,
or
O)
makes
Rh(III)
catalysis
an
attractive
step-economic
approach
value-added
molecules
from
readily
available
starting
materials.
Comparisons
contrasts
between
rhodium(III)
palladium(II)-catalyzed
made.
remarkable
diversity
structures
accessible
demonstrated
various
recent
examples,
a
proposed
mechanism
for
each
transformation
being
briefly
summarized
(critical
review,
138
references).
Chemical Reviews,
Год журнала:
2018,
Номер
119(4), С. 2192 - 2452
Опубликована: Ноя. 27, 2018
C–H
activation
has
surfaced
as
an
increasingly
powerful
tool
for
molecular
sciences,
with
notable
applications
to
material
crop
protection,
drug
discovery,
and
pharmaceutical
industries,
among
others.
Despite
major
advances,
the
vast
majority
of
these
functionalizations
required
precious
4d
or
5d
transition
metal
catalysts.
Given
cost-effective
sustainable
nature
earth-abundant
first
row
metals,
development
less
toxic,
inexpensive
3d
catalysts
gained
considerable
recent
momentum
a
significantly
more
environmentally-benign
economically-attractive
alternative.
Herein,
we
provide
comprehensive
overview
on
until
summer
2018.
Chemical Reviews,
Год журнала:
2016,
Номер
117(13), С. 8754 - 8786
Опубликована: Дек. 2, 2016
This
Review
summarizes
the
advancements
in
Pd-catalyzed
C(sp3)-H
activation
via
various
redox
manifolds,
including
Pd(0)/Pd(II),
Pd(II)/Pd(IV),
and
Pd(II)/Pd(0).
While
few
examples
have
been
reported
of
alkane
C-H
bonds,
many
activation/C-C
C-heteroatom
bond
forming
reactions
developed
by
use
directing
group
strategies
to
control
regioselectivity
build
structural
patterns
for
synthetic
chemistry.
A
number
mono-
bidentate
ligands
also
proven
be
effective
accelerating
directed
weakly
coordinating
auxiliaries,
which
provides
great
opportunities
reactivity
selectivity
(including
enantioselectivity)
functionalization
reactions.
Angewandte Chemie International Edition,
Год журнала:
2013,
Номер
53(1), С. 74 - 100
Опубликована: Ноя. 8, 2013
Abstract
Over
the
last
decade,
substantial
research
has
led
to
introduction
of
an
impressive
number
efficient
procedures
which
allow
selective
construction
CC
bonds
by
directly
connecting
two
different
CH
under
oxidative
conditions.
Common
these
methodologies
is
generation
reactive
intermediates
in
situ
activation
both
bonds.
This
strategy
was
introduced
group
Li
as
cross‐dehydrogenative
coupling
(CDC)
and
discloses
waste‐minimized
synthetic
alternatives
classic
rely
on
use
prefunctionalized
starting
materials.
Review
highlights
recent
progress
field
C
C
formations
provides
a
comprehensive
overview
existing
employed
methodologies.
Chemical Society Reviews,
Год журнала:
2016,
Номер
45(10), С. 2900 - 2936
Опубликована: Янв. 1, 2016
C–H
Activation
reactions
that
proceed
under
mild
conditions
are
more
attractive
for
applications
in
complex
molecule
synthesis.
Mild
transformations
reported
since
2011
reviewed
and
the
different
concepts
strategies
have
enabled
their
mildness
discussed.
Angewandte Chemie International Edition,
Год журнала:
2012,
Номер
51(41), С. 10236 - 10254
Опубликована: Сен. 20, 2012
The
use
of
coordinating
moieties
as
directing
groups
for
the
functionalization
aromatic
C-H
bonds
has
become
an
established
tool
to
enhance
reactivity
and
induce
regioselectivity.
Nevertheless,
with
regard
synthetic
applicability
activation,
there
is
a
growing
interest
in
transformations
which
group
can
be
fully
abandoned,
thus
allowing
direct
simple
benzene
derivatives.
However,
this
approach
requires
disclosure
new
strategies
achieve
control
selectivity.
In
review,
recent
advances
emerging
field
non-chelate-assisted
activation
are
discussed,
highlighting
some
most
intriguing
inspiring
examples
induction