Chemical Science,
Journal Year:
2023,
Volume and Issue:
14(30), P. 8109 - 8118
Published: Jan. 1, 2023
The
chemical
up-cycling
of
polymers
into
value-added
materials
offers
a
unique
opportunity
to
place
plastic
waste
in
new
value
chain
towards
circular
economy.
Herein,
we
report
the
selective
polystyrenes
and
polyolefins
C(sp3)-H
azidated
under
electrocatalytic
conditions.
functionalized
were
obtained
with
high
retention
mass
average
molecular
functionalization
through
chemo-selective
mangana-electrocatalysis.
Our
strategy
proved
be
broadly
applicable
variety
homo-
copolymers.
Polyethylene,
polypropylene
as
well
post-consumer
polystyrene
by
this
approach,
thereby
avoiding
use
hypervalent-iodine
reagents
stoichiometric
quantities
means
electrocatalysis.
This
study,
hence,
represents
oxidant-free
polymer
electro-oxidation.
electrocatalysis
scalable,
which
highlights
its
feature
for
green
hydrogen
economy
evolution
reaction
(HER).
Chemical Society Reviews,
Journal Year:
2021,
Volume and Issue:
50(14), P. 7941 - 8002
Published: Jan. 1, 2021
Electrochemistry
has
recently
gained
increased
attention
as
a
versatile
strategy
for
achieving
challenging
transformations
at
the
forefront
of
synthetic
organic
chemistry.
Electrochemistry's
unique
ability
to
generate
highly
reactive
radical
and
ion
intermediates
in
controlled
fashion
under
mild
conditions
inspired
development
number
new
electrochemical
methodologies
preparation
valuable
chemical
motifs.
Particularly,
recent
developments
electrosynthesis
have
featured
an
use
redox-active
electrocatalysts
further
enhance
control
over
selective
formation
downstream
reactivity
these
intermediates.
Furthermore,
electrocatalytic
mediators
enable
proceed
manner
that
is
mechanistically
distinct
from
purely
methods,
allowing
subversion
kinetic
thermodynamic
obstacles
encountered
conventional
synthesis.
This
review
highlights
key
innovations
within
past
decade
area
electrocatalysis,
with
emphasis
on
mechanisms
catalyst
design
principles
underpinning
advancements.
A
host
oxidative
reductive
are
discussed
grouped
according
classification
transformation
nature
electrocatalyst.
ACS Central Science,
Journal Year:
2021,
Volume and Issue:
7(2), P. 245 - 261
Published: Feb. 2, 2021
Since
the
definition
of
"12
Principles
Green
Chemistry"
more
than
20
years
ago,
chemists
have
become
increasingly
mindful
need
to
conserve
natural
resources
and
protect
environment
through
judicious
choice
synthetic
routes
materials.
The
direct
activation
functionalization
C–H
bonds,
bypassing
intermediate
functional
group
installation
is,
in
abstracto,
step
atom
economic,
but
numerous
factors
still
hinder
sustainability
large-scale
applications.
In
this
Outlook,
we
highlight
research
areas
seeking
overcome
challenges
activation:
pursuit
abundant
metal
catalysts,
avoidance
static
directing
groups,
replacement
oxidants,
introduction
bioderived
solvents.
We
close
by
examining
progress
made
subfield
aryl
borylation
from
its
origins,
highly
efficient
precious
Ir-based
systems,
emerging
3d
catalysts.
future
growth
field
will
depend
on
industrial
uptake,
thus
urge
researchers
strive
toward
sustainable
activation.
Green Synthesis and Catalysis,
Journal Year:
2021,
Volume and Issue:
2(2), P. 165 - 178
Published: March 29, 2021
There
is
a
resurgence
of
interests
in
organic
electrochemistry,
which
generally
accepted
as
green
synthetic
tool.
In
this
context,
many
electrochemical
methods
have
been
developed
the
past
decade
to
access
various
nitrogen-centered
radicals
(NCRs)
from
readily
available
precursors
controlled
fashion,
enabling
rapid
development
NCR-mediated
new
reactions
for
construction
nitrogen-containing
compounds.
review,
recent
advances
chemistry
electrochemically
generated
NCRs
are
critically
highlighted,
based
on
strategies
their
formation
and
types
NCRs.
Focus
put
mechanism
generation
different
applications.
Chemical Reviews,
Journal Year:
2023,
Volume and Issue:
123(19), P. 11269 - 11335
Published: Sept. 26, 2023
Late-stage
functionalization
(LSF)
constitutes
a
powerful
strategy
for
the
assembly
or
diversification
of
novel
molecular
entities
with
improved
physicochemical
biological
activities.
LSF
can
thus
greatly
accelerate
development
medicinally
relevant
compounds,
crop
protecting
agents,
and
functional
materials.
Electrochemical
synthesis
has
emerged
as
an
environmentally
friendly
platform
transformation
organic
compounds.
Over
past
decade,
electrochemical
late-stage
(eLSF)
gained
major
momentum,
which
is
summarized
herein
up
to
February
2023.
Chemical Reviews,
Journal Year:
2021,
Volume and Issue:
121(7), P. 4253 - 4307
Published: Feb. 26, 2021
Aliphatic
azides
are
a
versatile
class
of
compounds
found
in
variety
biologically
active
pharmaceuticals.
These
also
recognized
as
useful
precursors
for
the
synthesis
range
nitrogen-based
scaffolds
therapeutic
drugs,
compounds,
and
functional
materials.
In
light
growing
importance
aliphatic
both
chemical
biological
sciences,
vast
array
synthetic
strategies
preparation
structurally
diverse
have
been
developed
over
past
decades.
However,
to
date,
this
topic
has
not
subject
dedicated
review.
This
review
aims
provide
concise
overview
modern
access
that
emerged
since
2010.
The
discussed
azidation
reactions
include
(a)
C–C
multiple
bonds,
(b)
C–H
(c)
direct
transformation
vinyl
into
other
azides,
(d)
miscellaneous
azides.
We
critically
discuss
outcomes
generality
uniqueness
different
mechanistic
rationale
each
selected
reactions.
challenges
potential
opportunities
outlined.
Journal of the American Chemical Society,
Journal Year:
2022,
Volume and Issue:
144(3), P. 1187 - 1197
Published: Jan. 11, 2022
The
"magic
methyl"
effect,
a
dramatic
boost
in
the
potency
of
biologically
active
compounds
from
incorporation
single
methyl
group,
provides
simple
yet
powerful
strategy
employed
by
medicinal
chemists
drug
discovery
process.
Despite
significant
advances,
methodologies
that
enable
selective
C(sp3)–H
methylation
structurally
complex
agents
remain
very
limited.
In
this
work,
we
disclose
modular,
efficient,
and
for
α-methylation
protected
amines
(i.e.,
amides,
carbamates,
sulfonamides)
means
electrochemical
oxidation.
Mechanistic
analysis
guided
our
development
an
improved
protocol
on
basis
classic
Shono
oxidation
reaction,
which
features
broad
reaction
scope,
high
functional
group
compatibility,
operational
simplicity.
Importantly,
system
is
amenable
to
late-stage
functionalization
targets
containing
basic
nitrogen
groups
are
prevalent
medicinally
agents.
When
combined
with
organozinc-mediated
C–C
bond
formation,
enabled
direct
myriad
amine
derivatives
including
those
have
previously
been
explored
effect.
This
synthesis
thus
circumvents
multistep
de
novo
currently
necessary
access
such
has
potential
accelerate
efforts.