Journal of the American Chemical Society,
Год журнала:
2023,
Номер
145(15), С. 8417 - 8429
Опубликована: Март 23, 2023
Mechanistic
understanding
of
asymmetric
induction
plays
a
crucial
role
in
designing
new
catalytic
reactions.
Reported
herein
is
atroposelective
access
to
C-N
axially
chiral
isoquinolones
via
rhodium-catalyzed
C-H
activation
N-alkoxy
benzamides
and
annulation
with
imidoyl
sulfoxonium
ylides.
The
coupling
system
proceeded
excellent
functional
group
tolerance,
different
conditions
were
identified
afford
one
or
the
other
enantiomeric
product
each
enantioselectivity
for
representative
class
ylide
reagent,
thus
making
both
enantiomers
readily
available
using
same
catalyst.
Experimental
computational
studies
revealed
pathway
alkylation
enantio-determining
formal
nucleophilic
substitution-C-N
cyclization
that
mediated
by
rhodium
catalyst
σ-bond
metathesis
as
mechanism.
Computational
indicated
solvent-dependent
enatiodivergence
originated
from
levels
neutral
versus
cationic
species.
Chemical Society Reviews,
Год журнала:
2018,
Номер
47(17), С. 6603 - 6743
Опубликована: Янв. 1, 2018
The
present
review
is
devoted
to
summarizing
the
recent
advances
(2015-2017)
in
field
of
metal-catalysed
group-directed
C-H
functionalisation.
In
order
clearly
showcase
molecular
diversity
that
can
now
be
accessed
by
means
directed
functionalisation,
whole
organized
following
directing
groups
installed
on
a
substrate.
Its
aim
comprehensive
reference
work,
where
specific
group
easily
found,
together
with
transformations
which
have
been
carried
out
it.
Hence,
primary
format
this
schemes
accompanied
concise
explanatory
text,
are
ordered
sections
according
their
chemical
structure.
feature
typical
substrates
used,
products
obtained
as
well
required
reaction
conditions.
Importantly,
each
example
commented
respect
most
important
positive
features
and
drawbacks,
aspects
such
selectivity,
substrate
scope,
conditions,
removal,
greenness.
targeted
readership
both
experts
functionalisation
chemistry
(to
provide
overview
progress
made
last
years)
and,
even
more
so,
all
organic
chemists
who
want
introduce
way
thinking
for
design
straightforward,
efficient
step-economic
synthetic
routes
towards
molecules
interest
them.
Accordingly,
should
particular
also
scientists
from
industrial
R&D
sector.
overall
goal
promote
application
reactions
outside
research
dedicated
method
development
establishing
it
valuable
archetype
contemporary
R&D,
comparable
role
cross-coupling
play
date.
Chemical Reviews,
Год журнала:
2019,
Номер
119(14), С. 8701 - 8780
Опубликована: Июнь 25, 2019
Organosulfur
compounds
have
long
played
a
vital
role
in
organic
chemistry
and
the
development
of
novel
chemical
structures
architectures.
Prominent
among
these
organosulfur
are
those
involving
sulfur(IV)
center,
which
been
subject
countless
investigations
over
more
than
hundred
years.
In
addition
to
list
textbook
sulfur-based
reactions,
there
has
sustained
interest
organosulfur(IV)
recent
Of
particular
within
is
ease
with
synthetic
chemist
can
effect
wide
range
transformations
through
either
bond
formation
or
cleavage
at
sulfur.
This
review
aims
cover
developments
past
decade
molecules
provide
insight
into
both
reactions
critically
rely
on
this
versatile
element
diverse
scaffolds
that
thereby
be
synthesized.
Organic Chemistry Frontiers,
Год журнала:
2017,
Номер
5(6), С. 998 - 1002
Опубликована: Дек. 22, 2017
Sulfoxonium
ylides
acts
as
a
bifunctional
C2-synthon
in
Rh(iii)-catalyzed
redox-neutral
annulative
coupling
with
arenes
for
the
synthesis
of
N-heterocycles
and
carbocycles.
Organic Letters,
Год журнала:
2018,
Номер
20(5), С. 1396 - 1399
Опубликована: Фев. 22, 2018
A
rhodium-catalyzed
annulation
between
ethyl
benzimidates
and
α-
aroyl
sulfur
ylides
was
developed,
affording
a
series
of
pyrano[4,3,2-ij]isoquinoline
derivatives
in
moderate
to
good
yields
with
functional
group
compatibility.
The
procedure
featured
dual
ortho-C–H
functionalization
cyclization
one
pot.
optoelectronic
properties
those
fused
heteroarenes
were
tested
by
UV/vis
fluorescence
spectrometers.
Organic Letters,
Год журнала:
2019,
Номер
21(8), С. 2541 - 2545
Опубликована: Апрель 8, 2019
An
unprecedented
cascade
reaction
of
benzoyl
sulfoxonium
ylides
with
α-diazocarbonyl
compounds
leading
to
the
formation
highly
functionalized
naphthalenones
containing
a
β-ketosulfoxonium
ylide
moiety
is
presented.
Promisingly,
naphthalenone
derivative
thus
obtained
was
found
be
versatile
intermediate
toward
diversely
naphthalene
derivatives
including
substituted
1-naphthol,
2-hydroxynaphthalen-1(2H)-one,
naphthalen-1,2-dione,
and
2-(methylsulfinyl)naphthalen-1-ol.
Topics in Current Chemistry,
Год журнала:
2018,
Номер
376(3)
Опубликована: Апрель 13, 2018
Traditionally
employed
in
the
synthesis
of
small
ring
systems
and
rearrangement
chemistry,
sulfur-based
ylides
occupy
a
unique
position
toolbox
synthetic
organic
chemist.
In
recent
years
number
pioneering
researchers
have
looked
to
expand
application
these
unorthodox
reagents
through
use
transition
metal
catalysis.
The
strength
flexibility
such
combination
been
shown
be
key
importance
developing
powerful
novel
methodologies.
This
chapter
summarises
developments
metal-catalysed
sulfonium/sulfoxonium
ylide
reactions,
as
well
providing
historical
perspective.
overviewing
successes
this
area,
authors
hope
encourage
others
into
growing
field.
Advanced Synthesis & Catalysis,
Год журнала:
2018,
Номер
360(19), С. 3781 - 3787
Опубликована: Июль 12, 2018
Abstract
A
highly
chem‐
and
regioselective
synthesis
of
diversely
substituted
benzo[
a
]carbazoles
indolo[2,1‐
]‐isoquinolines
through
Rh(III)‐catalyzed
cascade
reactions
2‐arylindoles
with
sulfoxonium
ylides
is
presented.
To
be
specific,
treatment
2‐arylindoles,
2‐arylindole‐3‐carbaldehydes,
2‐arylindole‐3‐carbonitriles
or
2‐aryl‐3‐methylindoles
under
the
catalysis
Rh(III)
led
to
selective
formation
6‐aryl/alkyl
]carbazoles,
5‐acylbenzo[
6‐amino‐5‐acylbenzo[
12‐methylindolo[2,1‐
]isoquinolines,
respectively.
Mechanistically,
title
compounds
involves
process
including
metalation
inert
C(
sp
2
)−H
bond,
migratory
insertion
ylide
into
carbon‐metal
bond
via
an
in
situ
carbenoid
formation,
protodemetalation,
condensation.
our
knowledge,
this
first
example
which
β‐carbonyl
were
used
as
stable
carbene
precursors
bifunctional
C2
synthons
afford
]isoquinolines.
magnified
image
Angewandte Chemie International Edition,
Год журнала:
2018,
Номер
58(22), С. 7202 - 7236
Опубликована: Авг. 14, 2018
Abstract
Alkylation
of
arenes
is
one
the
most
fundamental
transformations
in
chemical
synthesis
and
leads
to
privileged
scaffolds
many
areas
science.
Classical
methods
for
introduction
alkyl
groups
are
mostly
based
on
Friedel–Crafts
reaction,
radical
additions,
metalation,
or
prefunctionalization
arene:
these
methods,
however,
suffer
from
limitations
scope,
efficiency,
selectivity.
Moreover,
they
innate
reactivity
starting
arene,
favoring
alkylation
at
a
certain
position
rendering
chains
other
positions
much
more
challenging.
This
can
be
addressed
by
use
directing
group
that
facilitates,
presence
metal
catalyst,
regioselective
C−H
bond.
These
directed
alkylations
bonds
will
comprehensively
summarized
this
Review.
ACS Catalysis,
Год журнала:
2020,
Номер
10(17), С. 9747 - 9757
Опубликована: Авг. 3, 2020
Transition-metal-catalyzed
C–H
activation
followed
by
oxidative
cyclization
with
unsaturated
coupling
partners
has
been
a
valuable
synthetic
tool
for
the
multiring
molecular
scaffolds.
This
Perspective
introduces
recent
progress
on
Cp*M-catalyzed
(M
=
Co,
Rh,
and
Ir)
direct
annulation
of
functionalized
arenes
terminal
alkynes
their
equivalents
through
bond
cleavage.
The
highlighted
examples
are
categorized
according
to
10
different
types
reagents
used
in
transformations.
representative
conditions,
selected
reaction
scope,
key
mechanistic
aspects
briefly
summarized.