Organic & Biomolecular Chemistry,
Год журнала:
2023,
Номер
21(18), С. 3784 - 3788
Опубликована: Янв. 1, 2023
An
NHC-catalyzed
[3
+
2
1]
annulation
of
vinyl
azides,
aldehydes,
and
Togni’s
reagents
was
reported.
The
cascade
involves
SET
redox
transformation,
denitrogenated
radical
migration,
C–N
coupling,
defluorinated
cyclization.
The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
89(18), С. 13128 - 13136
Опубликована: Сен. 11, 2024
Herein,
we
report
the
Ag-catalyzed
substrate-controlled
interrupted
radical
pathways
of
iminyl
radical.
The
benzylic
groups
played
a
crucial
role
in
pathway
selection
involving
series
dimerization
and
hydrolysis,
1,5-H
shift
followed
by
cascade
cyclization,
direct
N-(sp
Green Chemistry,
Год журнала:
2024,
Номер
26(21), С. 10804 - 10810
Опубликована: Янв. 1, 2024
We
present
an
efficient
and
sustainable
protocol
for
the
photoinduced-radical
hydrocyclization
of
isocyanides,
providing
a
united
route
to
assemble
diverse
α-unsubstituted
N-heteroarenes.
Green Synthesis and Catalysis,
Год журнала:
2023,
Номер
5(3), С. 195 - 199
Опубликована: Апрель 3, 2023
A
highly
efficient,
transition-metal-
and
light-free
approach
to
polyheterocycles
via
regioselective
cascade
radical
cyclization
is
developed.
The
redox-neutral
protocol
has
a
broad
substrate
scope
with
good
functional
group
tolerance
probably
undergoes
SET
process,
which
initiated
by
catalytic
amounts
of
quinone
in
combination
2.0
equiv.
Cs2CO3.
Organic & Biomolecular Chemistry,
Год журнала:
2023,
Номер
21(18), С. 3784 - 3788
Опубликована: Янв. 1, 2023
An
NHC-catalyzed
[3
+
2
1]
annulation
of
vinyl
azides,
aldehydes,
and
Togni’s
reagents
was
reported.
The
cascade
involves
SET
redox
transformation,
denitrogenated
radical
migration,
C–N
coupling,
defluorinated
cyclization.