Abstract
γ‐Nitro‐substituted
carbonyl
compounds
undergo
a
selenium
catalyzed
reductive
cyclization
with
CO
as
reducing
agent
to
yield
multi‐
fully‐substituted
pyrroles
(II)
and
(IV).
Organic Letters,
Год журнала:
2015,
Номер
17(3), С. 488 - 491
Опубликована: Янв. 16, 2015
Microwave-promoted
iminyl
radical
cyclizations
can
be
terminated
by
trapping
with
TEMPO,
affording
functionalized
adducts.
The
use
of
alkynes
as
acceptors
delivers
a
range
2-acylpyrroles
in
good
yields.
Toxic
and
hazardous
reagents,
which
are
frequently
employed
reactions,
not
required.
O-phenyl
oxime
ether
substrates
constructed
single
step
from
readily
available
ketones.
Organic Letters,
Год журнала:
2014,
Номер
17(2), С. 173 - 175
Опубликована: Дек. 31, 2014
A
ruthenium-catalyzed
reductive
amination
without
an
external
hydrogen
source
has
been
developed
using
carbon
monoxide
as
the
reductant
and
ruthenium(III)
chloride
(0.008–2
mol
%)
catalyst.
The
method
was
applied
to
synthesis
of
antianxiety
agent
ladasten.
Current Organic Synthesis,
Год журнала:
2022,
Номер
19(3), С. 393 - 413
Опубликована: Фев. 11, 2022
Abstract:
:
Organoselenium
chemistry
has
developed
as
an
important
tool
in
the
field
of
synthetic
and
medicinal
chemistry.
Various
organoselenium
reagents
have
been
used
successfully
to
achieve
different
organic
transformations
such
selenocyclizations,
oxyselenenylations
selenoxide
eliminations
etc.
Additionally,
potential
is
not
limited
their
use
stoichiometric
but
they
organocatalyst
number
transformations.
inorganic
oxidants
identified
terminal
regenerate
active
catalytic
specie.
In
this
review
article,
recent
progress
catalysis
being
highlighted
along
with
asymmetric
variants.
Current Organic Chemistry,
Год журнала:
2020,
Номер
24(11), С. 1196 - 1229
Опубликована: Май 28, 2020
Pyrroles
are
the
most
prevalent
heterocyclic
compounds,
which
present
as
basic
cores
in
many
natural
products,
such
vitamin
B12,
bile
pigments
like
bilirubin
and
biliverdin,
porphyrins
of
heme,
chlorophyll,
chlorins,
bacteriochlorins,
porphyrinogens.
The
biological
activities
compounds
having
pyrrole
analogs
include
antimicrobial
(antibacterial,
antifungal),
anti-cancer
(anti-cytotoxic,
antimitotic),
anti-tumor,
anti-hyperlipidemic,
anti-depressant,
anti-inflammatory,
antihyperglycemic,
antiproliferative,
anti-HIV
anti-viral
activities.
Accordingly,
significant
attention
has
been
paid
to
develop
competent
methods
for
synthesis
pyrroles
with
improved
yields
short
times.
This
review
gives
an
overview
different
using
easily
available
precursors
following
routes.
Synthesis
monosubstituted
2,5-dimethoxyfuran
dialkylacetylene
dicarboxylate
β-ketoester
1,2-dicarbonyl
1,3-dicarbonyl
1,3-dicarbonyl,
amine,
nitro
aldehyde
group
1,4-dicarbonyl
compound
amines
enones
moieties
acetylene
The Chemical Record,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 22, 2024
Abstract
The
conversion
of
a
functional
group
into
another
represents
the
core
organic
synthesis.
Within
arena
interconversions,
oxidative
and
reductive
transformations
occupy
privileged
position
development
new
sustainable,
selective,
general
methodologies
continue
to
attract
significant
interest.
Owing
versatility
their
chemistry,
selenium
compounds
offer
opportunities
achieve
both
oxidation
reduction
wide
range
groups.
Additionally,
possibility
generate
in
situ
active
oxidant
or
reducing
species
from
suitable
inert
precursors
enables
catalytic
processes.
In
this
review,
recent
advances
selenium‐mediated
with
particular
emphasis
on
cutting‐edge
researches
bringing
about
insights
comprehension
mechanistic
aspects,
will
be
discussed.
Organic & Biomolecular Chemistry,
Год журнала:
2016,
Номер
14(14), С. 3603 - 3607
Опубликована: Янв. 1, 2016
This
paper
presents
efficient
access
to
chiral
hydroxyimino
tetrahydrobenzofuranones
featuring
a
trifluoromethyl
group
at
an
all-carbon
quaternary
stereocenter.
Industrial & Engineering Chemistry Research,
Год журнала:
2017,
Номер
56(8), С. 1895 - 1902
Опубликована: Фев. 3, 2017
Regenerable
flue
gas
desulfurization
(FGD)
is
highly
attractive
because
of
the
transformation
sulfur
dioxide
(SO2)
to
high-value
products.
In
this
study,
selenium-assisted
SO2
reduction
by
carbon
monoxide
(CO)
in
liquid
phase
[dimethylformamide
(DMF)
+
water
(H2O)
mixture]
proposed
and
applied
FGD
process.
This
process
realizes
recycle
elemental
product
under
room
temperature.
Moreover,
results
show
that
both
selenium
catalyst
DMF
solvent
have
good
stability
can
be
well
recycled,
implying
economically
feasible.
Furthermore,
mechanism
CO
DMF/H2O
investigated.
Results
dissolves
solution
forms
Sen2–
species,
which
are
active
intermediates
promote
formation
product.