Radical Reactions with N-Heterocyclic Carbene (NHC)-Derived Acyl Azoliums for Access to Multifunctionalized Ketones
ACS Catalysis,
Год журнала:
2024,
Номер
14(11), С. 8270 - 8293
Опубликована: Май 13, 2024
As
one
of
the
most
important
key
intermediates,
NHC-bound
acylazolium-based
ionic
transformations
have
been
intensively
explored
in
past
two
decades.
With
expeditious
development
NHC-catalyzed
radical
recent
years,
acylazolium
chemistry
has
reached
another
level,
with
number
relevant
publications
increasing
significantly.
However,
a
summary
focused
on
acylations
NHC-derived
acyl
azoliums
classified
according
to
mechanistic
difference
not
reported.
Such
detailed
classification
and
deep
analysis
provide
opportunities
for
better
understanding
history
trend
this
field.
In
review,
reactions
N-heterocyclic
carbene
(NHC)-derived
are
systematically
introduced.
The
achievements
challenges
within
area
also
summarized
discussed
at
end.
Язык: Английский
Photoredox/NHC cooperative catalysis for alkylacylation of styrenes: An alternative method for the synthesis of γ-aminoketones
Ke-Yang Yu,
Fu Cheng,
Dong-Sen Duan
и другие.
Tetrahedron Letters,
Год журнала:
2025,
Номер
156, С. 155450 - 155450
Опубликована: Янв. 8, 2025
Язык: Английский
Visible Light-Mediated Monofluoromethylation/Acylation of Olefins by Dual Organo-Catalysis
Molecules,
Год журнала:
2024,
Номер
29(4), С. 790 - 790
Опубликована: Фев. 8, 2024
Monofluoromethyl
(CH2F)
motifs
exhibit
unique
bioactivities
and
are
considered
privileged
units
in
drug
discovery.
The
radical
monofluoromethylative
difunctionalization
of
alkenes
stands
out
as
an
appealing
approach
to
access
CH2F-containing
compounds.
However,
this
strategy
remains
largely
underdeveloped,
particularly
under
metal-free
conditions.
In
study,
we
report
on
visible
light-mediated
three-component
monofluoromethylation/acylation
styrene
derivatives
employing
NHC
organic
photocatalyst
dual
catalysis.
A
diverse
array
α-aryl-β-monofluoromethyl
ketones
was
successfully
synthesized
with
excellent
functional
group
tolerance
selectivity.
mild
CH2F
generation
from
NaSO2CFH2
holds
potential
for
further
applications
fluoroalkyl
chemistry.
Язык: Английский
Phosphonylacylation of Alkenes Enabled by Visible-Light-Induced N-Heterocyclic Carbene Catalysis
Organic Letters,
Год журнала:
2024,
Номер
26(8), С. 1711 - 1717
Опубликована: Фев. 20, 2024
Herein,
we
report
the
phosphonylacylation
of
alkenes
via
visible-light-induced
N-heterocyclic
carbene
(NHC)
catalysis
to
afford
a
series
γ-ketophosphonates
in
moderate
good
yields.
This
protocol
features
mild
conditions,
free
photocatalyst,
and
compatibility
functional
groups.
The
excited
Breslow
enolate
intermediate
was
proposed
undergo
single-electron
transfer
with
oxime
phosphonate
generate
corresponding
ketyl
radical
phosphonyl
radical.
Язык: Английский
1,2-Amidoarylcarbonylation of Styrenes to Access β-Acylamino Ketones by NHC-Catalyzed Radical Relay
The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
89(18), С. 13085 - 13092
Опубликована: Авг. 28, 2024
An
amidoarylcarbonylation
reaction
of
aromatic
aldehydes
and
olefins
with
Katritzky
pyridinium
salts
by
N-heterocyclic
carbene
(NHC)-catalyzed
radical
relay
to
construct
C-C
C-N
bonds
good
functional
group
tolerance
is
developed
for
the
synthesis
β-acylamino
ketones.
This
gentle
efficient
approach
offers
a
valuable
style
Mechanistic
studies
revealed
that
addition/coupling/elimination
cascade
process
was
involved
in
this
reaction.
Язык: Английский
Organocatalytic radical aminoacylation of alkenes for β-aminoketone synthesis
Ayisenbati Jialingbieke,
Xinying Hu,
Z. Liu
и другие.
Science China Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 14, 2024
Язык: Английский
Cooperative NHC and Photoredox Catalyzed Radical Aminoacylation of Alkenes to Tetrahydropyridazines
Wen‐Deng Liu,
Jiyuan Gao,
Jia‐Nan Mo
и другие.
Chemistry - A European Journal,
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 27, 2024
Tetrahydropyridazines
constitute
an
important
structural
motif
found
in
numerous
natural
products
and
pharmaceutical
compounds.
Herein,
we
report
aminoacylation
reaction
of
alkenes
that
enables
the
synthesis
1,4,5,6-tetrahydropyridazines
through
cooperative
N-heterocyclic
carbene
(NHC)
photoredox
catalysis.
This
approach
involves
6-endo-trig
cyclization
N-centered
hydrazonyl
radicals,
generated
via
single-electron
oxidation
hydrazones,
followed
by
a
radical-radical
coupling
step.
The
mild
process
tolerates
wide
range
common
functional
groups
affords
variety
tetrahydropyridazines
moderate
to
high
yields.
Preliminary
investigations
using
chiral
NHC
catalysts
demonstrate
potential
this
protocol
for
asymmetric
radical
reactions.
Язык: Английский
Dual N-Heterocyclic Carbene/Photoredox-Catalyzed Coupling of Acyl Fluorides and Alkyl Silanes
ACS Catalysis,
Год журнала:
2024,
Номер
unknown, С. 17642 - 17653
Опубликована: Ноя. 15, 2024
The
combination
of
N-heterocyclic
carbene
(NHC)
organocatalysis
with
photochemical
activation
is
becoming
increasingly
established
as
an
approach
for
conducting
radical
organic
reactions
under
mild
and
practical
conditions.
As
comparatively
easy
to
prepare
handle
compounds,
alkyl
silanes
are
attractive
substrates
chemistry
desilylative
mesolysis
the
corresponding
cations
known
be
rapid.
Here,
we
report
successful
application
benzyl
silane
derivatives
source
radicals
in
dual
NHC/photoredox-catalyzed
radical–radical
coupling
acyl
fluorides.
Relatively
electron-rich
reacted
smoothly
afford
ketones
generally
good
yields,
while
optimization
NHC
photocatalyst
allowed
a
wider
scope
including
primary
substrates.
Furthermore,
initial
experiments
revealed
that
organosilanes
bearing
N-,
O-
S-heteroatoms
can
also
serve
sources
these
Язык: Английский