Angewandte Chemie International Edition,
Journal Year:
2015,
Volume and Issue:
54(15), P. 4508 - 4511
Published: Feb. 20, 2015
The
first
highly
efficient
and
scalable
cobalt-catalyzed
directed
C-H
functionalization
with
carbene
precursors
is
presented.
This
methodology
provides
a
modular
route
towards
new
class
of
conjugated
polycyclic
hydrocarbons
tunable
emission
wavelengths
both
in
solution
the
solid
state.
Chemical Reviews,
Journal Year:
2018,
Volume and Issue:
119(4), P. 2192 - 2452
Published: Nov. 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 Society Reviews,
Journal Year:
2016,
Volume and Issue:
45(10), P. 2900 - 2936
Published: Jan. 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.
Chemical Society Reviews,
Journal Year:
2015,
Volume and Issue:
45(3), P. 546 - 576
Published: Oct. 28, 2015
The
advent
of
modern
C-H
functionalization
chemistries
has
enabled
medicinal
chemists
to
consider
a
synthetic
strategy,
late
stage
(LSF),
which
utilizes
the
bonds
drug
leads
as
points
diversification
for
generating
new
analogs.
LSF
approaches
offer
promise
rapid
exploration
structure
activity
relationships
(SAR),
generation
oxidized
metabolites,
blocking
metabolic
hot
spots
and
preparation
biological
probes.
This
review
details
toolbox
intermolecular
with
proven
applicability
drug-like
molecules,
classified
by
regioselectivity
patterns,
gives
guidance
on
how
systematically
develop
strategies
using
these
patterns
other
considerations.
In
addition,
number
examples
illustrate
have
been
used
impact
actual
discovery
chemical
biology
efforts.
ACS Catalysis,
Journal Year:
2015,
Volume and Issue:
6(2), P. 498 - 525
Published: Nov. 24, 2015
Catalytic
C–H
activation
has
emerged
as
a
powerful
tool
for
sustainable
syntheses.
In
the
recent
years,
notable
success
was
achieved
with
development
of
cobalt-catalyzed
functionalizations
either
in
situ
generated
or
single-component
cobalt-complexes
under
mild
reaction
conditions.
Herein,
progress
field
organometallic
is
reviewed
until
November
2015.
Chemical Reviews,
Journal Year:
2017,
Volume and Issue:
117(13), P. 9016 - 9085
Published: June 22, 2017
Research
and
industrial
interest
in
radical
C-H
activation/radical
cross-coupling
chemistry
has
continuously
grown
over
the
past
few
decades.
These
reactions
offer
fascinating
unconventional
approaches
toward
connecting
molecular
fragments
with
high
atom-
step-economy
that
are
often
complementary
to
traditional
methods.
Success
this
area
of
research
was
made
possible
through
development
photocatalysis
first-row
transition
metal
catalysis
along
use
peroxides
as
initiators.
This
Review
provides
a
brief
concise
overview
current
status
latest
methodologies
using
radicals
or
cations
key
intermediates
produced
via
activation.
includes
addition,
cascade
cyclization,
radical/radical
cross-coupling,
coupling
M-R
groups,
nucleophiles
(Nu).
Chemical Society Reviews,
Journal Year:
2018,
Volume and Issue:
47(15), P. 5786 - 5865
Published: Jan. 1, 2018
This
review
provides
an
overview
of
the
use
electrochemistry
as
appealing
platform
for
expediting
carbon–hydrogen
functionalization
and
carbon–nitrogen
bond
formation.
Chemical Reviews,
Journal Year:
2017,
Volume and Issue:
117(13), P. 9433 - 9520
Published: Feb. 13, 2017
As
two
coexisting
and
fast-growing
research
fields
in
modern
synthetic
chemistry,
the
merging
of
organocatalysis
C–H
bond
functionalization
is
well
foreseeable,
joint
force
along
this
line
has
been
demonstrated
to
be
a
powerful
approach
making
inert
more
viable,
predictable,
selective.
In
review,
we
provide
comprehensive
summary
over
past
decades.
The
review
arranged
by
types
bonds
including
alkane
C–H,
arene
vinyl
as
those
activated
benzylic
allylic
alpha
heteroatom
such
nitrogen
oxygen.
each
section,
discussion
classified
explicit
organocatalytic
mode
involved.
Chemical Reviews,
Journal Year:
2019,
Volume and Issue:
119(12), P. 6769 - 6787
Published: May 10, 2019
Photo-/electrochemical
catalyzed
oxidative
R1-H/R2-H
cross-coupling
with
hydrogen
evolution
has
become
an
increasingly
important
issue
for
molecular
synthesis.
The
dream
of
construction
C-C/C-X
bonds
from
readily
available
C-H/X-H
release
H2
can
be
facilely
achieved
without
external
chemical
oxidants,
providing
a
greener
model
bond
formation.
Given
the
great
influence
these
reactions
in
organic
chemistry,
we
give
summary
state
art
via
photo/electrochemistry,
and
hope
this
review
will
stimulate
development
synthetic
strategy
near
future.