Electrosynthesis of 1,4-diene derivatives bearing cyclopentene skeleton
Yaqi Qiao,
No information about this author
Xiaoqing Fan,
No information about this author
Chengcheng Yuan
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et al.
iScience,
Journal Year:
2025,
Volume and Issue:
28(3), P. 111976 - 111976
Published: Feb. 10, 2025
1,n-Dual
Π
systems
including
1,4-diene
derivatives
have
been
widely
used
as
the
elegant
radical
receptors
to
promote
cascade
additions
give
highly
functionalized
polycyclic
scaffolds.
However,
tedious
and
complicated
preparation
of
former
deters
broad
utilization
compromises
practical
value.
Herein,
a
straightforward
was
developed
from
easily
accessible
alkynes
γ,δ-unsaturated
carboxylic
acids
via
electrochemical
oxidation
cyclization
Hofmann
elimination.
This
transformation
features
with
good
excellent
yields,
functional
group
compatibility,
selectivity
without
any
Zaitsev
elimination
product
detected.
Language: Английский
Photoredox-Cobaloxime Catalysis for Selective Oxidative Dehydrogenative [4+2] Annulation of Imidazo-Fused Heterocycles with Alkenes
Ailong Shao,
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Yuanyuan Li,
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Yuxue Ding
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et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(13), P. 2529 - 2534
Published: March 21, 2024
A
selective
oxidative
[4+2]
annulation
of
alkenes
with
imidazo-fused
heterocycles
has
been
developed
by
using
the
synergistic
combination
photoredox
and
cobaloxime
catalysts.
It
allows
facile
access
to
various
imidazole-fused
polyaromatic
scaffolds
accompanied
H2
evolution.
This
protocol
features
high
regioselectivity
as
well
a
broad
substrate
scope.
Detailed
mechanistic
studies
indicate
that
twice
electron/H
transfer
processes
facilitated
this
catalytic
system
achieve
π-extension
alkenes.
Language: Английский
Electrosynthesis of Highly Functionalized Polycyclic N-Heteroaromatics through Cascade Radical Cyclization and Alkoxylation in Batch and Continuous-Flow
Jiawei Chen,
No information about this author
Yaqi Qiao,
No information about this author
Wenjing Guan
No information about this author
et al.
ACS Sustainable Chemistry & Engineering,
Journal Year:
2023,
Volume and Issue:
11(50), P. 17728 - 17738
Published: Dec. 6, 2023
Electrochemical
radical
cascade
cyclization
has
been
recognized
as
a
powerful,
straightforward,
and
environmentally-friendly
synthetic
tool
to
give
highly
functionalized
polycyclic
aromatic
compounds
but
remains
challenging
difficult
because
of
the
instability
intermediates
under
electrolysis
conditions,
especially
using
user-friendly
undivided
cell.
Herein,
we
report
novel
electrosynthesis
pyridine-fused
N-heteroaromatics
through
dehydrogenative
alkoxylation
oxidant-free
conditions.
This
electrochemical
synthesis
methodology
features
green
mild
reaction
good
functional
group
tolerance,
use
readily
available
substrates.
Moreover,
attributed
flow
cells,
steady
production
large-scale
preparation
can
be
conveniently
achieved
only
small
amounts
electrolytes.
Language: Английский
De novo synthesis of 6-6-5 fused-systems through electrochemical decarboxylation and radical domino additions
Chengcheng Yuan,
No information about this author
Guanru Liu,
No information about this author
Wenjing Guan
No information about this author
et al.
Green Chemistry,
Journal Year:
2024,
Volume and Issue:
26(19), P. 10308 - 10313
Published: Jan. 1, 2024
An
oxidant
and
quaternary
ammonium
salt-free
electrosynthesis
of
6-6-5
fused
systems
was
developed
with
excellent
atom
step
economy.
Language: Английский
Recent Advances in the Electrochemical Functionalization of Imidazoheterocycles
Advanced Synthesis & Catalysis,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 18, 2024
Abstract
Imidazoheterocycles
have
extensive
applications
in
the
pharmaceutical
industry
and
agrochemicals.
A
comprehensive
overview
has
been
provided
on
current
advancements
electrochemical
functionalization
of
imidazo‐fused
heterocycles,
which
classified
into
ten
different
types
reactions.
Electrochemical
synthesis
emerged
as
a
highly
effective
method
for
producing
organic
molecules,
especially
context
sustainable
development.
Employing
electrons
traceless
oxidant,
several
C−H
reactions
heterocycles
achieved
at
either
C3
or
C5
positions.
Electrons
may
serve
reducing
agent
to
synthesize
pyridine
rings
that
are
partially
fully
saturated
imidazo[1,2‐
]pyridines.
The
purpose
review
is
attract
interest
scientific
community
promote
additional
research
imidazoheterocycles
using
methods.
Language: Английский