Chemical Communications,
Год журнала:
2023,
Номер
59(19), С. 2726 - 2738
Опубликована: Янв. 1, 2023
We
describe
recent
achievements
in
the
visible-light-induced
chemical
transformations
of
methylenecyclopropanes
(MCPs),
including
ring-opening
reactions,
cyclopropane-producing
and
reactions
via
a
non-classical
radical
clock.
ACS Catalysis,
Год журнала:
2023,
Номер
13(23), С. 15331 - 15339
Опубликована: Ноя. 13, 2023
Two
C(sp3)
radicals
cross-coupling
as
a
straightforward
method
for
constructing
C(sp3)–C(sp3)
bonds
has
attracted
extensive
attention
from
chemists.
Unfortunately,
the
strategy
is
challenging
due
to
unexpected
reactions
of
transient
radicals,
such
homocoupling
and
hydrogen
atom
transfer.
In
this
regard,
capturing
open-shell
by
metal
catalysts
can
effectively
enhance
selectivity
radical
via
formation
more
stable
organometallic
intermediates.
Herein,
we
disclose
selective
two
through
dual
combination
iridium-catalyst-mediated
decarboxylation
nickel-catalyst-mediated
continuous
capture
radicals.
This
mild
atom-efficient
Ni-catalyzed
N-cyclization–alkylation
protocol
was
employed
prepare
various
alkyl–alkyl
cross-coupled
products.
The
synthetic
applications
methodology
are
demonstrated
late-stage
functionalization
drugs,
natural
products,
biomolecules.
Organic Chemistry Frontiers,
Год журнала:
2024,
Номер
11(15), С. 4207 - 4213
Опубликована: Янв. 1, 2024
A
general
photochemical
approach
for
the
oximation
of
activated
alkenes
to
synthesize
diverse
oximes
without
catalysts
is
described.
The
simple
and
modular
method
offers
a
new
perspective
chemists
rapidly
obtain
various
radical
intermediates.
Advanced Synthesis & Catalysis,
Год журнала:
2023,
Номер
365(21), С. 3690 - 3703
Опубликована: Сен. 16, 2023
Abstract
A
multifaceted
study
on
the
effect
of
various
factors
efficiency
photocyclization
naphthofuran
O‐acyl
oximes
was
performed.
It
showed
that
without
any
additives
or
in
presence
electron
acceptors,
reaction
occurs
by
a
radical
pathway
and
with
low
chemoselectivity,
while
DABCO
promotes
intramolecular
cyclization
to
give
naphthofuroquinolines
(NFQs)
34–87%
yields.
The
iminyl
formed
under
UV
irradiation
due
single
transfer
(SET)
N−O
bond
cleavage
undergoes
selective
homolytic
aromatic
substitution
(HAS)
formation
new
C−N
bond.
This
route
quinoline‐annulated
scaffolds
is
based
use
both
as
an
agent
proton
acceptor.
Chemical Communications,
Год журнала:
2023,
Номер
59(19), С. 2726 - 2738
Опубликована: Янв. 1, 2023
We
describe
recent
achievements
in
the
visible-light-induced
chemical
transformations
of
methylenecyclopropanes
(MCPs),
including
ring-opening
reactions,
cyclopropane-producing
and
reactions
via
a
non-classical
radical
clock.