The Journal of Organic Chemistry,
Год журнала:
2023,
Номер
88(20), С. 14697 - 14707
Опубликована: Сен. 29, 2023
A
facile
and
practical
approach
for
the
preparation
of
substituted
pyrimidines
from
ketones,
NH4OAc,
N,N-dimethylformamide
dimethyl
acetal
has
been
described.
This
NH4I-promoted
three-component
tandem
reaction
affords
a
broad
range
in
acceptable
yields
under
metal-
solvent-free
conditions.
The
present
methodology
features
advantages
simple
easily
available
starting
materials,
conditions,
substrate
scope
with
good
functional
group
tolerance,
gram-scale
synthesis.
Green Chemistry,
Год журнала:
2020,
Номер
22(5), С. 1720 - 1725
Опубликована: Янв. 1, 2020
An
eco-friendly
visible-light-induced
decarboxylative
acylation
of
quinoxalin-2(1H)-ones
and
α-oxo
carboxylic
acids
with
air
as
the
oxidant
under
external-photocatalyst-free
conditions
was
established.
Green Chemistry,
Год журнала:
2019,
Номер
22(2), С. 433 - 438
Опубликована: Ноя. 26, 2019
The
first
example
of
selective
oxidation
sulfides
to
sulfones
and
sulfoxides
using
molecular
oxygen
under
clean
conditions
was
established.
desired
products
could
be
easily
collected
through
recrystallization
in
large-scale
preparation.
ACS Sustainable Chemistry & Engineering,
Год журнала:
2019,
Номер
7(24), С. 19993 - 19999
Опубликована: Ноя. 8, 2019
By
using
ambient
air
as
an
oxidant,
various
N-acylated
3-aminoquinoxalin-2(1H)-ones
were
efficiently
synthesized
through
visible-light-promoted
rhodamine
B-catalyzed
amidation
reaction
of
quinoxalin-2(1H)-ones
and
amides
under
metal-free
strong
oxidant-free
conditions.
Green Synthesis and Catalysis,
Год журнала:
2021,
Номер
2(2), С. 233 - 236
Опубликована: Апрель 8, 2021
An
electrochemical
transient
iodination
and
coupling
reaction
has
been
designed
for
constructing
selenylated
4-anilinocoumarins
via
the
domino
reactions
of
diorganyl
diselenides
under
base-,
chemical
oxidant-
external
electrolyte-free
conditions.
Organic Chemistry Frontiers,
Год журнала:
2024,
Номер
11(18), С. 5122 - 5129
Опубликована: Янв. 1, 2024
This
study
demonstrates
a
strategy
involving
photoinduced
energy
transfer
for
decarboxylative
Minisci
C–H
(amino)alkylation
of
heteroarenes
employing
diverse
oxime
esters
(from
carboxylic
acids)
as
(amino)alkylating
reagents.
