Electrosynthesis of Highly Functionalized Quinolines through Radical Annulation–Polar Addition Cascade
Organic Letters,
Год журнала:
2024,
Номер
26(35), С. 7330 - 7335
Опубликована: Авг. 22, 2024
Synthesis
of
diversely
functionalized
quinoline-2-carboxylates
is
illustrated
through
electrochemical
cross-dehydrogenative
coupling
between
N-aryl
glycinates
and
methylenecyclopropanes.
An
extensive
range
distinct
functionalities
well-compatible
under
these
transition-metal-
oxidant-free
mild
conditions,
contributing
to
a
broad
substrate
scope
practical
applicability.
Cyclic
voltammetric
measurements
control
experiments
suggested
formal
[4
+
2]
cycloaddition
involving
radical
intermediates,
followed
by
cyclopropyl
ring
opening
nucleophilic
polar
addition,
consecutively
fabricating
C–C
C–N
bonds.
Язык: Английский
Photocatalyzed [2+1] cyclization of alkenes and silylated trifluorodiazoethanes: facile entry into (difluoromethylene)cyclopropanes
Science China Chemistry,
Год журнала:
2023,
Номер
66(11), С. 3141 - 3147
Опубликована: Июль 28, 2023
Язык: Английский
Photochemical Divergent Ring-Closing Metathesis of 1,7-Enynes: Efficient Synthesis of Spirocyclic Quinolin-2-ones
Organic Letters,
Год журнала:
2024,
Номер
26(31), С. 6664 - 6669
Опубликована: Июль 30, 2024
A
photocatalytic
method
for
the
ring-closing
1,7-enyne
metathesis
using
α-amino
radical
as
an
alkene
deconstruction
auxiliary
is
present.
Preliminary
mechanistic
studies
suggest
that
intramolecular
1,5-hydrogen
atom
transfer
key
to
generation
and
β-scission
of
radical,
while
dearomatization
arenes
ring
opening
cyclopropanes
are
construct
spirocyclic
quinolin-2-ones.
This
approach
highlights
potential
metathesis,
providing
a
green,
efficient,
step-economical
way
synthesis
Язык: Английский
Ni/Photoredox-catalyzed coupling of aryl bromides and methylenecyclopropanes via selective distal bond cleavage
Organic Chemistry Frontiers,
Год журнала:
2024,
Номер
11(18), С. 5033 - 5043
Опубликована: Янв. 1, 2024
A
series
of
1,1-dibenzylethylene
derivatives
were
obtained
in
moderate-to-good
yields
via
double
coupling
aryl
bromides
and
methylenecyclopropanes
Ni/photoredox
catalysis.
The
critical
roles
nickel
this
reaction
disclosed.
Язык: Английский
Visible light-mediated hydrogen atom transfer and proton transfer for the conversion of (2-vinylaryl)methanol derivatives to aryl aldehydes or aryl ketones
Organic Chemistry Frontiers,
Год журнала:
2023,
Номер
10(23), С. 5876 - 5885
Опубликована: Янв. 1, 2023
A
visible-light-mediated
strategy
for
the
efficient
conversion
of
(2-vinylaryl)methanol
derivatives
to
aryl
aldehydes
or
ketones
has
been
developed.
The
plausible
reaction
mechanism
verified
by
a
series
mechanistic
studies.
Язык: Английский
Cyclization reactions of cyclopropane derivatives with conjugated carbo- and heterosystems
Russian Chemical Reviews,
Год журнала:
2024,
Номер
93(3), С. RCR5111 - RCR5111
Опубликована: Март 1, 2024
The
strained
structure
of
cyclopropanes
serves
as
a
kind
trigger
for
variety
chemical
transformations.
Among
others,
processes
involving
conjugated
unsaturated
systems
are
particular
interest.
bonds
characterized
by
the
possibility
flexibly
varying
their
reactivity
up
to
full
involvement
in
This
review
is
first
consider
options
implementing
idea
combining
strain
energy
and
synthetic
capacity
within
single
concept.
A
detailed
analysis
activated
numerous
carbodiene
heterodiene
presented.<br>
bibliography
includes
289
references.
Язык: Английский
Photocatalytic annulative cyanoalkyletherification of 1,6-enynes toward 1-indanones
Tetrahedron,
Год журнала:
2023,
Номер
139, С. 133438 - 133438
Опубликована: Апрель 29, 2023
Язык: Английский
Nickel/ligand loading-controlled divergent and selective coupling between redox-active methylenecyclopropanes and ArBr
Organic Chemistry Frontiers,
Год журнала:
2024,
Номер
11(20), С. 5720 - 5730
Опубликована: Янв. 1, 2024
Diverse
alkyne
and
dibenzylethylene
derivatives
were
obtained
via
selective
coupling
of
redox-active
MCPs
ArBr
under
Ni/photoredox
catalysis.
The
nickel/ligand
loading
tuning
method
played
a
crucial
role
in
this
divergent
synthesis
protocol.
Язык: Английский