Organic Chemistry Frontiers,
Год журнала:
2021,
Номер
8(14), С. 3746 - 3751
Опубликована: Янв. 1, 2021
A
photoredox-catalyzed
reaction
of
oximes,
rongalite
and
electrophiles
is
accomplished,
affording
pyrrole-substituted
aliphatic
sulfones
or
sulfonamides
in
moderate
to
good
yields.
Organic Chemistry Frontiers,
Год журнала:
2022,
Номер
9(7), С. 1937 - 1942
Опубликована: Янв. 1, 2022
An
iron-catalyzed
dearomative
spirocyclization
of
biaryl
ynones
with
sodium
metabisulfite
and
cycloketone
oxime
esters
is
developed
for
the
construction
sulfonated
spiro[5,5]trienones.
European Journal of Organic Chemistry,
Год журнала:
2023,
Номер
26(25)
Опубликована: Апрель 25, 2023
Abstract
Compounds
containing
sulfonyl‐derived
functional
groups
have
received
intensive
attention
owing
to
their
widespread
applications
in
life
science,
pharmaceuticals
and
materials
science.
To
access
this
type
of
compounds,
the
multi‐component
sulfonylation
reactions
relying
on
sulfur
dioxide
(SO
2
)
insertion
strategy
emerged
as
novel
attractive
approaches
past
decade.
The
utilization
SO
surrogates
for
multicomponent
(MCRs)
improved
reaction
flexibility
step
economy.
Moreover,
some
advances
been
achieved
challenging
but
practical
asymmetric
MCRs
construction
high
value‐added
chiral
sulfones.
This
review
aims
summarize
progress
made
involving
from
2019
2022,
point
out
potentials
challenges
field.
Organic Chemistry Frontiers,
Год журнала:
2021,
Номер
8(19), С. 5403 - 5409
Опубликована: Янв. 1, 2021
A
visible-light
photoredox-catalyzed
four
component
reaction
of
quinoxalin-2(1
H
)-ones,
alkenes,
aryldiazonium,
and
sodium
metabisulfite
leading
to
sulfone-containing
)-ones
has
been
developed.
Organic Chemistry Frontiers,
Год журнала:
2021,
Номер
8(14), С. 3746 - 3751
Опубликована: Янв. 1, 2021
A
photoredox-catalyzed
reaction
of
oximes,
rongalite
and
electrophiles
is
accomplished,
affording
pyrrole-substituted
aliphatic
sulfones
or
sulfonamides
in
moderate
to
good
yields.