Organic Letters,
Год журнала:
2020,
Номер
22(13), С. 5140 - 5144
Опубликована: Июнь 17, 2020
An
efficient
and
regioselective
synthesis
of
fused
polycyclic
furo[3,4-c]indolo[2,1-a]isoquinolines
through
Rh(III)-catalyzed
cascade
C–H
activation/annulation/lactonization
2-arylindoles
4-hydroxy-2-alkynoates
has
been
developed.
This
reaction
displays
high
step
economy
efficiency
tolerates
various
functional
groups.
The
titled
exhibit
fluorescence
emission.
Chemistry - An Asian Journal,
Год журнала:
2020,
Номер
15(14), С. 2092 - 2109
Опубликована: Июнь 5, 2020
2-Pyridone
is
a
ubiquitous
motif
in
natural
products,
drug
molecules,
ligands
catalysis
and
organic
materials.
There
necessity
of
direct
step-economic
methods
for
the
construction
2-pyridone
based
molecules.
Strategically,
primary
developments
have
led
to
C3-functionalizations
due
inherent
reactivity
this
center.
Despite
this,
many
elegant
transition
metal-catalysed
been
established
introduce
versatile
functional
groups
at
C4,
C5
C6-position
via
C-H
bond
functionalizations.
This
minireview
focuses
on
categorized
introduction
different
scaffolds
beyond
C3-selectivity
discusses
substrate
scope,
limitations
plausible
mechanistic
details.
Organic Letters,
Год журнала:
2018,
Номер
20(8), С. 2204 - 2207
Опубликована: Апрель 4, 2018
In
this
paper,
a
Cu(II)/Ag(I)-catalyzed
cascade
reaction
of
anthranils
with
sulfonylhydrazone
to
construct
2-phenyl-3-sulfonyl
disubstituted
quinoline
derivatives
under
mild
conditions
was
studied.
The
mechanism
study
indicated
that
involves
radical
addition,
and
new
C-C,
C-N,
C-S
bonds
were
constructed
in
one
step.
The Journal of Organic Chemistry,
Год журнала:
2017,
Номер
82(17), С. 8933 - 8942
Опубликована: Авг. 7, 2017
An
efficient
copper(I)-catalyzed
direct
regioselective
arylamination
of
various
heterocyclic
N-oxides
was
achieved
successfully
under
redox-neutral
conditions
using
anthranils
as
arylaminating
reagents.
The
developed
protocol
is
simple,
straightforward,
and
economic
with
a
broad
range
substrate
scope.
dual
functional
groups
in
the
final
molecules
were
utilized
to
construct
structurally
functionally
diverse
nitrogen-containing
organic
π-conjugated
systems.
Organic Letters,
Год журнала:
2020,
Номер
22(13), С. 5140 - 5144
Опубликована: Июнь 17, 2020
An
efficient
and
regioselective
synthesis
of
fused
polycyclic
furo[3,4-c]indolo[2,1-a]isoquinolines
through
Rh(III)-catalyzed
cascade
C–H
activation/annulation/lactonization
2-arylindoles
4-hydroxy-2-alkynoates
has
been
developed.
This
reaction
displays
high
step
economy
efficiency
tolerates
various
functional
groups.
The
titled
exhibit
fluorescence
emission.