Photoredox Nickel-Catalyzed Radical Cyclization of N-Arylacrylamides with Alkyl Bromides
Yanling Liu,
No information about this author
Lei Shi,
No information about this author
Xian‐Chen He
No information about this author
et al.
Organic & Biomolecular Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
We
present
a
photoredox
nickel-catalyzed
intermolecular
cyclization
between
N
-arylacrylamides
and
readily
accessible
alkyl
bromides,
which
affords
diverse
range
of
3,3-disubstituted
oxindoles
in
moderate
to
high
yields.
Language: Английский
Cu(II)/Photoredox-Catalyzed Aminoacylation of Vinyl Bromides
Organic Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 24, 2025
A
novel
C–C
coupling
reaction
of
vinyl
bromides
with
carboxamides
has
been
developed
through
Cu(OAc)2/photocatalysis.
This
process
features
regioselective
carboxamido
carbon-vinylation
under
mild
conditions.
Mechanistic
studies
suggest
that
the
formation
an
acyl-Cu(I)
intermediate
plays
a
crucial
role
regard
to
enabling
this
transformation.
Language: Английский
Photoinduced pinacol coupling of carbon-carbon bonds via triethoxysilane or Hantzsch Ester
Jianhua Liu,
No information about this author
Gelan Wang,
No information about this author
Chen Chen
No information about this author
et al.
Molecular Catalysis,
Journal Year:
2025,
Volume and Issue:
579, P. 115088 - 115088
Published: April 5, 2025
Language: Английский
Nickel/Photoredox Dual-Catalyzed, Regioselective 1,2-Carboacylation of Alkenes via Synergistic Alkyl and Benzoyl Radical Coupling
Xian‐Chen He,
No information about this author
Jie Gao,
No information about this author
Yang Li
No information about this author
et al.
Organic Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 2, 2025
A
regioselective
1,2-carboacylation
protocol
of
alkenes
via
nickel/photoredox
dual
catalysis
has
been
successfully
developed
under
mild
conditions.
wide
range
alkyl
bromides,
α-oxocarboxylic
acids,
and
styrenes
proved
to
be
compatible
the
optimized
conditions,
affording
corresponding
products
in
up
91%
yields.
Mechanistically,
key
success
this
approach
is
temporal
orchestration
radical
generation:
nickel-catalyzed
halogen
atom
transfer
(XAT)
for
bromides
photoredox-driven
decarboxylation
acids.
Language: Английский