Journal of the American Chemical Society,
Год журнала:
2022,
Номер
144(42), С. 19456 - 19465
Опубликована: Окт. 5, 2022
Highly
chemo-
and
regioselective
semihydrogenation
of
alkynes
is
significant
challenging
for
the
synthesis
functionalized
alkenes.
Here,
a
sequential
self-template
method
used
to
synthesize
amorphous
palladium
sulfide
nanocapsules
(PdSx
ANCs),
which
enables
electrocatalytic
terminal
in
H2O
with
excellent
tolerance
easily
reducible
groups
(e.g.,
C–I/Br/Cl,
C═O)
metal
center
deactivating
skeletons
quinolyl,
carboxyl,
nitrile).
Mechanistic
studies
demonstrate
that
specific
σ-alkynyl
adsorption
via
carbon
negligible
alkene
on
isolated
Pd2+
sites
ensure
successful
various
alkenes
outstanding
time-irrelevant
selectivity
wide
potential
range.
The
key
hydrogen
radical
intermediates
are
validated
by
electron
paramagnetic
resonance
high-resolution
mass
spectrometry.
Gram-scale
4-bromostyrene
expedient
preparation
deuterated
precursors
drugs
D2O
show
promising
applications.
Impressively,
PdSx
ANCs
can
be
applied
prevailing
thermocatalytic
alkyne
using
H2.
Chemical Science,
Год журнала:
2020,
Номер
11(34), С. 9109 - 9114
Опубликована: Янв. 1, 2020
To
date
the
majority
of
diene
carboxylation
processes
afford
α,δ-dicarboxylated
product,
selective
mono-carboxylation
dienes
is
a
significant
challenge
and
major
product
reported
under
transition
metal
catalysis
arises
from
at
α-carbon.
Herein
we
report
new
electrosynthetic
approach,
that
does
not
rely
on
sacrificial
electrode,
method
allows
unprecedented
direct
access
to
carboxylic
acids
derived
δ-position.
In
addition,
α,δ-dicarboxylic
acid
or
α,δ-reduced
alkene
can
be
easily
accessed
by
simple
modification
reaction
conditions.
Journal of the American Chemical Society,
Год журнала:
2022,
Номер
144(42), С. 19456 - 19465
Опубликована: Окт. 5, 2022
Highly
chemo-
and
regioselective
semihydrogenation
of
alkynes
is
significant
challenging
for
the
synthesis
functionalized
alkenes.
Here,
a
sequential
self-template
method
used
to
synthesize
amorphous
palladium
sulfide
nanocapsules
(PdSx
ANCs),
which
enables
electrocatalytic
terminal
in
H2O
with
excellent
tolerance
easily
reducible
groups
(e.g.,
C–I/Br/Cl,
C═O)
metal
center
deactivating
skeletons
quinolyl,
carboxyl,
nitrile).
Mechanistic
studies
demonstrate
that
specific
σ-alkynyl
adsorption
via
carbon
negligible
alkene
on
isolated
Pd2+
sites
ensure
successful
various
alkenes
outstanding
time-irrelevant
selectivity
wide
potential
range.
The
key
hydrogen
radical
intermediates
are
validated
by
electron
paramagnetic
resonance
high-resolution
mass
spectrometry.
Gram-scale
4-bromostyrene
expedient
preparation
deuterated
precursors
drugs
D2O
show
promising
applications.
Impressively,
PdSx
ANCs
can
be
applied
prevailing
thermocatalytic
alkyne
using
H2.