Green Chemistry,
Journal Year:
2024,
Volume and Issue:
27(3), P. 560 - 565
Published: Dec. 17, 2024
Utilizing
a
robotic
visible-light
photocatalytic
system,
we
realized
metal-free
and
100%
atom-economical
method
for
the
difunctionalization
of
alkynes
with
high
stereoselectivity
regioselectivity.
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(12), P. 3442 - 3450
Published: Jan. 1, 2024
Here,
we
report
a
visible-light-mediated
[2
+
2
1]
cascade
cyclization
of
1,6-enynes
with
thiols,
providing
sulfur-containing
polycyclic
molecules
in
moderate
to
good
yields.
Molecules,
Journal Year:
2024,
Volume and Issue:
29(15), P. 3620 - 3620
Published: July 31, 2024
Synthetic
radicals
have
intrinsic
power
for
cascading
and
multifunctional
reactions
to
construct
diverse
molecular
scaffolds.
In
the
previous
review
series,
we
covered
1,2-difunctionalizations,
remote
1,3-,
1,4-,
1,5-,
1,6-,
1,7-difunctionalizations,
addition
followed
by
cyclization
reactions,
cycloaddition-initiated
difunctionalizations.
Presented
in
this
paper
are
radical
addition-initiated
trifunctionalization
of
alkenes,
alkynes,
their
derivatives.
After
initial
addition,
there
different
pathways,
such
as
group
or
hydrogen
atom
transfer,
cyclization,
coupling,
complete
second
third
functionalizations.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(44), P. 9498 - 9502
Published: Oct. 31, 2024
Here,
we
report
an
intermolecular
carboacylation
of
terminal
alkynes
with
tertiary
and
secondary
alkyltrifluoroborates
as
well
acyl
chlorides
via
photoredox/nickel
dual
catalysis,
affording
a
varity
stereodefined
trisubstituted
enones
in
good
to
excellent
yields
E
stereoselectivity,
through
radical
relay
process.
This
redox-neutral
protocol
exhibits
functional
group
tolerance,
exclusive
regio-
broad
compatibility
various
alkyltrifluoroborates.
Abstract
Herein,
we
introduce
a
novel
method
for
the
synthesis
of
S
‐substituted
isothiourea
compounds
via
selective
1,2‐carboimination
between
oxime
esters
as
bifunctional
reagents
and
C=S
bond
isothiocyanates
under
visible‐light
catalysis.
This
approach
deviates
from
conventional
methods
by
precisely
modulating
substrate
electronics
to
selectively
functionalize
over
C=N
bond,
eliminating
need
strong
bases
high
temperatures
bypassing
formation
thiourea
intermediates.
Consequently,
this
protocol
enables
efficient
one‐step
‐alkyl
isothioureas,
with
featuring
mild
reaction
conditions,
operational
simplicity
broad
scope.
Green Chemistry,
Journal Year:
2024,
Volume and Issue:
27(3), P. 560 - 565
Published: Dec. 17, 2024
Utilizing
a
robotic
visible-light
photocatalytic
system,
we
realized
metal-free
and
100%
atom-economical
method
for
the
difunctionalization
of
alkynes
with
high
stereoselectivity
regioselectivity.