The Journal of Organic Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 19, 2024
We
developed
a
method
for
allowing
cascade
cyclization
of
2-nitrochalcones
with
pyrazoles,
imidazole,
and
indazole
in
the
presence
CuI
catalyst,
DBU
base,
THF
solvent.
The
conditions
were
tolerant
an
array
useful
functionalities
including
ester,
nitro,
cyano,
halogen
groups.
A
mechanistic
consideration
was
also
provided,
as
H2O2
presumably
byproduct.
Our
appears
to
be
rare
example
directly
prepare
C3-heterocyclic
unprotected
indoles.
New Journal of Chemistry,
Journal Year:
2023,
Volume and Issue:
47(43), P. 19822 - 19826
Published: Jan. 1, 2023
A
DBU-promoted
three-component
cascade
annulation
of
3-oxo-3-phenylpropanenitriles,
(
E
)-chalcones
and
selenium
powder
has
been
proposed
for
the
synthesis
tetrasubstituted
selenophenes.
ChemistrySelect,
Journal Year:
2024,
Volume and Issue:
9(23)
Published: June 18, 2024
Abstract
An
efficient
method
for
the
construction
of
2,4‐diarylbenzo[4,5]thieno[3,2‐
d
]pyrimidines
through
base‐promoted
one‐pot
three‐component
tandem
reactions
o
‐nitrochalcones,
benzamidine
hydrochlorides,
and
elemental
sulfur
is
described.
The
salient
features
this
protocol
are
use
cheap
abundant
source,
readily
available
starting
materials,
transition‐metal‐free
mild
conditions,
satisfactory
yield,
simple
workup
procedures.
This
transformation
can
also
carry
out
on
gram
scale.
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(21), P. 6144 - 6149
Published: Jan. 1, 2024
We
developed
a
protocol
for
the
synthesis
of
PIITOs
from
maleimides
and
nitroenamines.
This
strategy
featured
[2
+
2
2]
cycloaddition
with
heating
mixture
substrates
1
DMF
without
any
catalyst.
The Journal of Organic Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 19, 2024
We
developed
a
method
for
allowing
cascade
cyclization
of
2-nitrochalcones
with
pyrazoles,
imidazole,
and
indazole
in
the
presence
CuI
catalyst,
DBU
base,
THF
solvent.
The
conditions
were
tolerant
an
array
useful
functionalities
including
ester,
nitro,
cyano,
halogen
groups.
A
mechanistic
consideration
was
also
provided,
as
H2O2
presumably
byproduct.
Our
appears
to
be
rare
example
directly
prepare
C3-heterocyclic
unprotected
indoles.