Three-component dicarbofunctionalization of allylamines via nucleopalladation pathway: unlocking vicinal and geminal selectivity
Chemical Science,
Год журнала:
2024,
Номер
15(13), С. 4890 - 4896
Опубликована: Янв. 1, 2024
A
palladium(
ii
)-catalyzed
vicinal
and
geminal
selective
dicarbofunctionalization
of
allylamine
embedded
in
a
removable
picolinamide
auxiliary
is
developed
by
exploiting
nucleopalladation-triggered
intermolecular
three-component
coupling
reaction.
Язык: Английский
Regioselective intermolecular carboamination of allylamines via nucleopalladation: empowering three-component synthesis of vicinal diamines
Chemical Science,
Год журнала:
2024,
Номер
unknown
Опубликована: Янв. 1, 2024
Intermolecular
carboamination
of
allyl
amines
under
Pd(
ii
)-catalysis
is
reported,
expediting
the
synthesis
vicinal
diamines
embedded
in
a
functionally
enriched
linear
carbon
framework
with
high
yields
and
exclusive
Markovnikov
selectivity.
Язык: Английский
Pd-Catalyzed Three-Component 1,1-Carboamination of 4-Pentenoic Acid
Organic Letters,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 13, 2025
Herein,
we
describe
a
method
to
achieve
the
three-component
1,1-carboamination
of
4-pentenoic
acid
by
palladium
catalysis,
successfully
constructing
δ-lactam
derivatives.
The
protocol
features
excellent
1,1-regioselectivity,
high
step
and
atom
economy,
good
functional
group
tolerance.
Язык: Английский
Pd-catalyzed Markovnikov selective oxidative amination of 4-pentenoic acid
Chemical Communications,
Год журнала:
2024,
Номер
60(71), С. 9626 - 9629
Опубликована: Янв. 1, 2024
A
palladium-catalyzed
and
ligand-controlled
strategy
for
the
Markovnikov
selective
oxidative
amination
of
4-pentenoic
acid
has
been
described.
Язык: Английский
Palladium Catalysis: Dependence of the Efficiency of C–N Bond Formation on Carboxylate Ligand and Metal Carboxylate or Carboxylic Acid Additive
ACS Omega,
Год журнала:
2024,
Номер
unknown
Опубликована: Март 8, 2024
The
Pd-catalyzed
inter-
and
intramolecular
reactions
of
nitrogen
compounds
are
often
carried
out
with
palladium
carboxylates,
sometimes
in
the
presence
carboxylic
acids
or
alkali
metal
carboxylates.
This
Mini-Review
highlights
dependence
reaction
efficiency
on
nature
ligand
carboxylate
additives.
proposed
mechanisms
presented
with,
as
far
possible,
personal
comments.
Язык: Английский
Visible-Light-Induced Difunctionalization of 3-Butenoic Acid with Bromodifluoromethyl Heteroarylsulfones
Organic Letters,
Год журнала:
2024,
Номер
26(30), С. 6449 - 6453
Опубликована: Июль 22, 2024
Herein,
we
report
a
visible-light-induced
iridium-promoted
direct
bifunctionalization
of
3-butenoic
acid
with
bromodifluoromethyl
heteroarylsulfones.
This
methodology
enables
the
concurrent
introduction
difluoromethyl
heteroarylsulfone
and
bromine
groups
into
under
mild
reaction
conditions.
Various
Язык: Английский