Chemical Science,
Год журнала:
2022,
Номер
13(19), С. 5616 - 5621
Опубликована: Янв. 1, 2022
An
unprecedented
report
on
Rh-catalyzed
meta
-C–H
alkynylation
of
arenes,
aided
by
a
weakly
coordinating
cyano-based
directing
template,
was
developed
using
bromoalkynes
as
the
coupling
partner.
Green Synthesis and Catalysis,
Год журнала:
2022,
Номер
3(3), С. 203 - 211
Опубликована: Фев. 28, 2022
Thioether
skeletons
are
widely
present
in
drugs,
natural
products,
functional
materials,
and
life
science.
In
the
past
decade,
selective
C–H
functionalization
of
thioethers
has
been
extensively
studied
to
construct
novel
thioether
derivatives.
This
mini-review
systematically
introduces
recent
advances
field
direct
α-C(sp3)-H
thioethers.
Organic Letters,
Год журнала:
2020,
Номер
22(5), С. 1807 - 1812
Опубликована: Фев. 17, 2020
A
hindered
β-amino
amide
transient
directing
group
effects
di-trans-arylation
of
cyclohexanecarbaldehydes.
The
N-substituents
are
shown
to
affect
yield
and
can
enhance
the
rate
arylation
compared
with
α-amino
acid.
Addition
a
pyridone
ligand
further
enhanced
reactivity.
reaction
is
successful
for
range
aryl
iodides,
various
substituted
cyclohexane
carboxaldehydes,
providing
functionalized
products
from
simple
feedstocks.
mechanism
proposed
evoking
enamine.
Chemical Science,
Год журнала:
2022,
Номер
13(19), С. 5616 - 5621
Опубликована: Янв. 1, 2022
An
unprecedented
report
on
Rh-catalyzed
meta
-C–H
alkynylation
of
arenes,
aided
by
a
weakly
coordinating
cyano-based
directing
template,
was
developed
using
bromoalkynes
as
the
coupling
partner.