Organic Letters,
Journal Year:
2019,
Volume and Issue:
21(16), P. 6534 - 6538
Published: July 31, 2019
An
efficient
electro-oxidative
C–H/N–H
activation
with
1,3-diynes
has
been
achieved
a
robust
earth-abundant
cobalt
catalyst.
The
electrochemical
C–H
functionalization
was
accomplished
ample
scope
and
remarkable
functional
group
compatibility
in
simple
undivided
cell.
This
protocol
avoids
the
utilization
of
stoichiometric
cost-intensive
chemical
oxidants
activation,
thus
forming
hydrogen
as
only
byproduct.
ACS Catalysis,
Journal Year:
2019,
Volume and Issue:
9(9), P. 7690 - 7696
Published: July 12, 2019
Synthetically
meaningful
isoindolones
were
accessed
by
cupraelectro-catalyzed
C–H
activation
with
electricity
as
terminal
oxidant.
Thus,
a
versatile,
inexpensive,
and
nontoxic
Cu(OAc)2
catalyst
enabled
broadly
applicable
C–H/N–H
functionalizations
on
electron-rich
electron-deficient
benzamides
distinct
functional
group
tolerance
resource-economy.
Detailed
mechanistic
studies
provided
strong
support
for
alkynylation
mechanism
through
fast
metalation,
which
likewise
set
the
stage
C–H/C–C
in
decarboxylative
fashion.
ChemSusChem,
Journal Year:
2019,
Volume and Issue:
12(13), P. 3023 - 3027
Published: March 21, 2019
Abstract
Electrochemical
oxidative
C−H/N−H
activations
with
isocyanides
have
been
realized
a
versatile
cobalt
catalyst.
The
widely
applicable
catalysis
manifold
further
enabled
electrooxidative
carbonylations
carbon
monoxide
under
ambient
conditions.
C−H
functionalizations
were
efficiently
ample
scope
and
outstanding
functional
group
tolerance
in
user‐friendly
undivided
cell
setup.
Organic Letters,
Journal Year:
2019,
Volume and Issue:
21(9), P. 3228 - 3231
Published: April 18, 2019
A
new
anode
strategy
for
accessing
xanthen-9-azoles
via
an
electrochemical
C(sp3)-H/N-H
cross-coupling
of
xanthenes
with
azoles
is
described.
This
reaction
proceeds
efficiently
a
broad
scope
both
and
N-H-free
under
metal-
additional
oxidant-free
conditions
represents
access
to
direct
incorporation
important
N-heterocycle
units
into
the
resulting
xanthenes.
Organic Letters,
Journal Year:
2019,
Volume and Issue:
21(16), P. 6534 - 6538
Published: July 31, 2019
An
efficient
electro-oxidative
C–H/N–H
activation
with
1,3-diynes
has
been
achieved
a
robust
earth-abundant
cobalt
catalyst.
The
electrochemical
C–H
functionalization
was
accomplished
ample
scope
and
remarkable
functional
group
compatibility
in
simple
undivided
cell.
This
protocol
avoids
the
utilization
of
stoichiometric
cost-intensive
chemical
oxidants
activation,
thus
forming
hydrogen
as
only
byproduct.