Organic Letters,
Год журнала:
2022,
Номер
24(24), С. 4459 - 4463
Опубликована: Июнь 13, 2022
Herein
we
report
C(sp2)-S
cross-coupling
reactions
of
aryl
iodides
and
arylsulfonyl
hydrazides
under
ligand-enabled,
Au(I)/Au(III)
redox
catalysis.
This
strategy
operates
mild
reaction
conditions,
requires
no
prefunctionalized
coupling
partner,
works
across
several
iodides.
The
utility
this
protocol
is
highlighted
through
the
synthesis
various
medicinally
relevant
biaryl
sulfones.
mechanism
supported
with
control
experiments,
mass
spectrometry,
NMR
studies.
Chemical Reviews,
Год журнала:
2020,
Номер
120(9), С. 4141 - 4168
Опубликована: Апрель 2, 2020
Cyclic
(alkyl)-
and
(aryl)-(amino)carbenes
(CAACs
CAArCs)
are
stronger
σ-donors
π-acceptors
than
imidazol-2-ylidenes
imidazolidin-2-ylidenes,
the
well-known
N-heterocyclic
carbenes
(NHCs).
Consequently,
they
form
strong
bonds
with
coinage
metals
stabilize
both
low
high
oxidation
states.
This
Review
shows
that
CAACs
CAArCs
have
allowed
for
isolation
of
copper
gold
complexes
were
believed
to
be
only
transient
intermediates.
has
not
a
better
understanding
mechanism
known
processes
but
also
led
development
novel
metal-catalyzed
reactions.
In
addition
their
role
in
homogeneous
catalysis,
CAAC
CAArC
metal
recently
found
applications
medicinal
chemistry,
as
well
materials
science.
When
possible,
performance
ligands
compared
those
classical
NHCs.
Chemical Reviews,
Год журнала:
2021,
Номер
121(14), С. 8478 - 8558
Опубликована: Фев. 8, 2021
The
catalyst-directed
divergent
synthesis,
commonly
termed
as
"divergent
catalysis",
has
emerged
a
promising
technique
it
allows
chartering
of
structurally
distinct
products
from
common
substrates
simply
by
modulating
the
catalyst
system.
In
this
regard,
gold
complexes
powerful
catalysts
they
offer
unique
reactivity
profiles
compared
to
various
other
transition
metal
catalysts,
primarily
due
their
salient
electronic
and
geometrical
features.
Owing
tunable
soft
π-acidic
nature,
not
only
evolved
superior
contenders
for
catalyzing
reactions
alkynes,
alkenes,
allenes
but
also,
more
intriguingly,
have
been
found
provide
reaction
pathways
over
π-acid
such
Ag,
Pt,
Pd,
Rh,
Cu,
In,
Sc,
Hg,
Zn,
etc.
recent
past
witnessed
renaissance
in
examples
wherein,
choosing
or
fine-tuning
ligands,
counteranions
oxidation
states
itself,
complete
switch
was
observed.
However,
reviews
documenting
are
sporadic;
result,
most
reports
kind
remained
scattered
literature,
thereby
hampering
further
development
burgeoning
field.
By
conceptualizing
idea
"Divergent
Gold
Catalysis
(DGC)",
review
aims
consolidate
all
unified
approach
necessary
pave
way
advancement
exciting
area.
Based
on
factors
governing
divergence
product
formation,
an
explicit
classification
DGC
provided.
To
gain
fundamental
understanding
observed
reactivities
selectivities,
is
accompanied
mechanistic
insights
at
appropriate
places.
Chemical Reviews,
Год журнала:
2020,
Номер
121(14), С. 8364 - 8451
Опубликована: Сен. 23, 2020
Over
the
past
decade
organometallic
chemistry
of
gold(III)
has
seen
remarkable
advances.
This
includes
synthesis
first
examples
several
compound
classes
that
have
long
been
hypothesized
as
being
part
catalytic
cycles,
such
alkene,
alkyne,
CO
and
hydride
complexes,
important
catalysis-relevant
reaction
steps
at
last
demonstrated
for
gold,
like
migratory
insertion
β-H
elimination
reactions.
Also,
pathways
were
already
known,
example
generation
intermediates
by
oxidative
addition
their
reductive
elimination,
are
much
better
understood.
A
deeper
understanding
fundamental
reactivity
revealed
unexpected
mechanistic
avenues,
which
can
open
when
barriers
reactions
other
metals
would
be
regarded
"standard"
too
high.
review
summarizes
evaluates
these
developments,
together
with
applications
in
catalysis,
emphasis
on
insight
gained
investigations.
Chemistry - A European Journal,
Год журнала:
2019,
Номер
26(7), С. 1442 - 1487
Опубликована: Окт. 28, 2019
Abstract
Transition‐metal‐catalyzed
cross‐coupling
reactions
are
central
to
many
organic
synthesis
methodologies.
Traditionally,
Pd,
Ni,
Cu,
and
Fe
catalysts
used
promote
these
reactions.
Recently,
studies
have
showed
that
both
homogeneous
heterogeneous
Au
can
be
for
activating
selective
Here,
an
overview
of
the
past
studies,
current
trends,
future
directions
in
field
gold‐catalyzed
coupling
is
presented.
Design
strategies
accomplish
homocoupling
under
conditions,
computational
experimental
mechanistic
their
applications
diverse
fields
critically
reviewed.
Specific
topics
covered
are:
oxidant‐assisted
oxidant‐free
reactions;
strain‐assisted
dual
photoredox
catalysis;
bimetallic
synergistic
mechanisms
reductive
elimination
processes;
enzyme‐mimicking
chemistry;
cluster
surface
plasmonic
catalysis.
In
relevant
sections,
theoretical
I
/Au
III
chemistry
discussed
predictions
from
calculations
compared
with
observations
derive
useful
design
strategies.
Chemical Society Reviews,
Год журнала:
2021,
Номер
50(18), С. 10422 - 10450
Опубликована: Янв. 1, 2021
This
review
highlights
a
decade-long
journey
of
Au-catalyzed
1,2-difunctionalization
reactions
C–C
multiple
bonds
that
have
been
realized
due
to
the
productive
integration
Au(
i
)/Au(
iii
)catalysis
with
unique
π-activation
mode
gold
complexes.
Chemical Reviews,
Год журнала:
2021,
Номер
121(14), С. 8311 - 8363
Опубликована: Фев. 9, 2021
In
this
contribution,
we
provide
an
overview
of
the
main
avenues
that
have
emerged
in
gold
coordination
chemistry
during
last
years.
The
unique
properties
motivated
research
chemistry,
and
especially
regarding
applications
compounds
catalysis,
medicine,
materials
chemistry.
advances
synthesis
knowledge
been
possible
with
design
novel
ligands
becoming
relevant
motifs
allowed
preparation
elusive
complexes
area
research.
Strong
donor
easily
modulable
electronic
steric
properties,
such
as
stable
singlet
carbenes
or
cyclometalated
ligands,
decisive
stabilization
gold(0)
species,
fluoride
complexes,
hydrides,
unprecedented
π
cluster
derivatives.
These
new
important
not
only
from
fundamental
structure
bonding
studies
but
also
for
sophisticated
catalysts
to
improve
activity
selectivity
organic
transformations.
Moreover,
they
enabled
facile
oxidative
addition
gold(I)
gold(III)
a
plethora
specific
properties.
Advanced Synthesis & Catalysis,
Год журнала:
2021,
Номер
363(11), С. 2723 - 2739
Опубликована: Апрель 7, 2021
Abstract
Indole
is
one
of
the
most
important
heterocycles
in
organic
synthesis,
natural
products,
and
drug
discovery.
Recently,
tremendous
advances
selective
functionalization
indoles
have
been
reported.
Although
powered
by
transition
metal
catalysis,
exceedingly
useful
methods
absence
metals
also
In
this
review,
we
provide
an
overview
reactions
that
published
last
years
with
a
focus
on
recent
advances,
aims,
future
trends.
The
review
organized
positional
selectivity
type
used
for
functionalization.
particular,
discuss
major
transition‐metal‐catalyzed
C−H
at
classical
C2/C3
positions,
remote
C4/C7
cross‐coupling,
transition‐metal‐free
magnified
image
Journal of the American Chemical Society,
Год журнала:
2022,
Номер
144(16), С. 7089 - 7095
Опубликована: Апрель 18, 2022
Presented
herein
is
the
first
report
of
enantioselective
Au(I)/Au(III)
redox
catalysis,
enabled
by
a
newly
designed
hemilabile
chiral
(P,N)-ligand
(ChetPhos).
The
potential
this
concept
has
been
demonstrated
development
1,2-oxyarylation
and
1,2-aminoarylation
alkenes
which
provided
direct
access
to
medicinally
relevant
3-oxy-
3-aminochromans
(up
88%
yield
99%
ee).
DFT
studies
were
carried
out
unravel
enantiodetermining
step,
revealed
that
stronger
trans
influence
phosphorus
allows
selective
positioning
substrate
in
C2-symmetric
environment
present
around
nitrogen,
imparting
high
level
enantioselectivity.
Angewandte Chemie International Edition,
Год журнала:
2022,
Номер
61(12)
Опубликована: Янв. 21, 2022
Abstract
The
first
C−SCF
3
/SeCF
cross‐coupling
reactions
using
gold
redox
catalysis
[(MeDalphos)AuCl],
AgSCF
or
Me
4
NSeCF
,
and
organohalides
as
substrates
are
reported.
new
methodology
enables
a
one‐stop
shop
synthesis
of
aryl/alkenyl/alkynyl
trifluoromethylthio‐
selenoethers
with
broad
substrate
scope
(>60
examples
up
to
97
%
isolated
yield).
method
is
scalable,
its
robustness
evidenced
by
the
late‐stage
functionalization
various
bioactive
molecules,
which
makes
this
reaction
an
attractive
alternative
in
for
pharmaceutical
agrochemical
research
development.