The Royal Society of Chemistry eBooks,
Год журнала:
2023,
Номер
unknown, С. 147 - 167
Опубликована: Фев. 15, 2023
Heterocycles
containing
chalcogens
as
heteroatoms
or
embedded
in
several
different
functional
groups
founded
interesting
applications
medicinal
chemistry,
coordination
and
materials.
Recent
development
on
their
preparation
is
reported
here.
The Journal of Organic Chemistry,
Год журнала:
2022,
Номер
87(6), С. 4273 - 4283
Опубликована: Март 4, 2022
We
report
herein
an
alternative
method
for
the
synthesis
of
seleno-dibenzocycloheptenones
and
seleno-spiro[5.5]trienones
through
radical
cyclization
biaryl
ynones
in
presence
diorganyl
diselenides,
using
Oxone
as
a
green
oxidizing
agent.
The
reactions
were
conducted
acetonitrile
solvent
sealed
tube
at
100
°C.
protocol
is
operationally
simple
scalable,
exhibits
high
regioselectivity,
allows
24
dibenzocycloheptenones/spiro[5.5]trienones
yields
up
to
99%,
17
which
are
unpublished
compounds.
Additionally,
synthetic
transformations
prepared
compounds,
such
oxidation
reduction
reactions,
demonstrated.
Abstract
Presently,
the
major
cornerstone
of
research
community
is
to
develop
green
as
well
sustainable
protocols
involving
inexpensive
catalysts
and/or
reagents
without
usage
hazardous
solvents
under
globally
friendlier
conditions
in
order
shelter
both
mankind
and
environment.
Therefore,
needless
say,
there
always
a
supreme
need
surrogate
older,
costlier
unsafe
strategies
with
novel
economically
environmental
benign
ones.
To
this
context,
recent
past,
oxone®
(triple
salt),
very
cheap
oxidizing
agent
having
chemical
formula
2KHSO
5
⋅
KHSO
4
K
2
SO
enwrapped
unique
characteristics
like
easy
handling,
non‐toxic,
safe,
eco‐friendly,
non‐polluting,
stable,
nicely
soluble
water,
addition
its
utility
for
large‐scale
synthesis
etc.
Bearing
importance
versatile
reagent
mind,
we
envisioned
update
advances
made
direction.
Consequently,
particular
review
article,
developments
arena
oxone
chemistry
covering
from
2013
2020
have
been
revealed
no
report
appeared
literature
after
wonderful
Chem.
Rev.
published
by
group
Hussain
2013.
Herein,
comprehensive
detail
variety
oxidative
transformations
along
complete
plausible
mechanistic
steps
exposed.
For
sure,
present
would
be
helpful
tool
scientific
not
only
working
area
organic
but
also
researchers
other
branches
science
technologies
well.
Chemistry - An Asian Journal,
Год журнала:
2023,
Номер
18(5)
Опубликована: Янв. 17, 2023
The
versatility
of
isocoumarin
frameworks
offers
the
privilege
to
access
many
pharmacological
targets.
This
unique
heterocycle
core
present
in
natural
products
and
complex
organic
molecules
contribute
medicinal
chemistry
as
anti-cancer,
anti-inflammatory
immunomodulatory
agents.
attractive
properties
exhibited
by
its
analogues
urged
scientists
explore
their
synthetic
analogues.
In
regard
myriads
methodologies,
we
have
compiled
a
review
update
covering
all
articles
that
been
published
towards
synthesis
3-substituted
3,4-disubstituted
isocoumarins.
Additionally,
also
highlighted
systematic
survey
catalytic
methods
for
along
with
scope
diverse
functionalizations
plausible
mechanistic
aspects.
The Journal of Organic Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 8, 2025
A
novel
green
methodology
for
the
Oxone-mediated
oxidative
addition
of
alkenes
via
intramolecular
acyl
migration
has
been
developed.
This
transformation
utilizes
N-acyl-N-sulfonyl
allylamines
and
diselenides
as
starting
materials,
with
Oxone
serving
oxidant
water
a
partial
oxygen
source.
The
protocol
enables
synthesis
series
β-acyloxy-γ-selenyl
sulfonamides
high
to
excellent
yields
demonstrates
broad
substrate
scope.
Notably,
yield
was
maintained
in
gram-scale
experiments,
highlighting
scalability
this
method.
Through
comprehensive
control
we
have
elucidated
reaction
mechanism,
which
involves
rapid
radical
generation,
predominant
cationic
pathway,
migration.
study
presents
an
efficient
environmentally
benign
approach
valuable
sulfonamides.
The Journal of Organic Chemistry,
Год журнала:
2022,
Номер
87(22), С. 15050 - 15060
Опубликована: Окт. 27, 2022
We
describe
here
for
the
first
time
synthesis
of
2-(chalcogenyl)-3H-benzo[f]chromenes
and
new
3-(phenylselanyl)-2H-chromenes
by
radical
or
electrophilic
cyclization
propargylic
aryl
ethers
in
presence
diorganyl
diselenides
ditellurides
using
Oxone
as
a
green
oxidant
acetonitrile
solvent
sealed
tube
at
100
°C.
In
this
study,
thirty-one
chalcogenylchromenes
with
broad
substrate
scope
were
prepared
moderate
to
excellent
yields
(50-98%),
including
compounds
derived
from
natural
products.
Catalysts,
Год журнала:
2023,
Номер
13(10), С. 1369 - 1369
Опубликована: Окт. 15, 2023
The
last
decade
has
witnessed
significant
progress
in
the
development
of
novel
synthetic
methods
for
preparation
a
variety
new
functionalized
and
condensed
compounds
via
reactions
organic
dichalcogenides
with
acetylenic
derivatives.
present
review
highlights
recent
developments
synthesis
organoselenium
based
on
diselenides
acetylenes
over
past
few
years.
discussion
mainly
focuses
literature
data
5
It
is
worth
noting
that
lion’s
share
this
material
devoted
to
catalytic
electrophile-mediated
aromatic
compounds,
containing
triple
bond
nucleophilic
functional
groups.
Ultrasonics Sonochemistry,
Год журнала:
2021,
Номер
80, С. 105834 - 105834
Опубликована: Ноя. 16, 2021
In
organic
and
inorganic
synthesis
in
analytical
methods,
an
external
conventional
heat
source
is
usually
applied
to
carry
out
a
chemical
reaction
at
high
temperature,
or
extraction
procedure.
the
last
decades,
use
of
ultrasound
as
alternative
energy
has
become
interesting
field
research
these
topics
South
Cone
region
(Argentina,
Chile,
Uruguay,
Southern
Brazil
Paraguay).
For
this
reason,
present
review,
covering
period
2009
mid-2021,
compilation
ultrasound-assisted
synthetic
methodologies.