Synthetic Chemistry in Flow: From Photolysis & Homogeneous Photocatalysis to Heterogeneous Photocatalysis
Sitong Feng,
No information about this author
Ren Su
No information about this author
ChemSusChem,
Journal Year:
2024,
Volume and Issue:
17(16)
Published: April 12, 2024
Abstract
Photocatalytic
synthesis
of
value‐added
chemicals
has
gained
increasing
attention
in
recent
years
owing
to
its
versatility
driving
many
important
reactions
under
ambient
conditions.
Selective
hydrogenation,
oxidation,
coupling,
and
halogenation
with
a
high
conversion
the
reactants
have
been
realized
using
designed
photocatalysts
batch
reactors
small
volumes
at
laboratory
scale;
however,
scaling‐up
remains
critical
challenge
due
inefficient
utilization
incident
light
active
sites
photocatalysts,
resulting
poor
catalytic
performance
that
hinders
practical
applications.
Flow
systems
are
considered
one
solutions
for
applications
light‐driven
experienced
great
success
photolytic
homogeneous
photocatalysis,
yet
their
heterogeneous
photocatalysis
still
development.
In
this
perspective,
we
summarized
progress
photocatalytic
synthetic
chemistry
performed
flow
from
view
reactor
design
special
focus
on
photocatalysis.
The
advantages
limitations
different
systems,
as
well
some
considerations
strategies
discussed.
Language: Английский
Photochemical synthesis in inorganic chemistry
Rimsha Kanwal,
No information about this author
Riyadh R. Al-Araji,
No information about this author
Ahmad H. Ibrahim
No information about this author
et al.
Reviews in Inorganic Chemistry,
Journal Year:
2024,
Volume and Issue:
44(3), P. 323 - 337
Published: Feb. 16, 2024
Abstract
In
the
last
few
decades,
photochemistry
has
great
influence
on
all
type
of
synthetic
processes.
While
photochemical
synthesis
is
emerging
field
in
inorganic
chemistry
as
it
impart
various
magnificent
properties
to
materials
that
are
used
for
nano-sized
giant
supramolecular
structures.
There
many
based
approaches
like
electron,
atom,
energy
transfer
depending
upon
need
product
where
one
can
switch
pathway.
A
variety
compounds
have
been
synthesized
dienes,
nitrides,
indoles,
gold
nano-particles
and
structures
using
route.
Photochemical
applications
artificial
photosynthesis
fluorophores.
Language: Английский
Recent advances exploiting reactive intermediates generated via continuous flow chemistry
Current Opinion in Green and Sustainable Chemistry,
Journal Year:
2024,
Volume and Issue:
47, P. 100907 - 100907
Published: March 13, 2024
Reactive
intermediates
are
transient
high-energy
species
playing
a
pivotal
role
in
the
synthesis
of
organic
molecules.
Continuous
flow
processing
is
frequently
exploited
generating
plethora
reactive
situ
followed
by
their
rapid
transformation
to
target
Reactor
miniaturisation
along
with
high
heat
and
mass
transfer
rates
key
features
that
these
processes
provide
for
additional
benefits
such
as
safety
scalability.
This
short
review
highlights
recent
advances
field
chemistry
generation
use
photochemical
reactions,
low-temperature
sequences
well
related
transformations.
Language: Английский
Rapid and Safe Continuous‐Flow Simmons‐Smith Cyclopropanation using a Zn/Cu Couple Column
Advanced Synthesis & Catalysis,
Journal Year:
2023,
Volume and Issue:
366(4), P. 710 - 716
Published: Sept. 14, 2023
Abstract
Flow
chemistry
has
recently
opened
new
windows
thanks
to
the
safer
use
of
hazardous
and
sensitive
reagents.
Furthermore,
flow
procedures
usually
outperform
their
batch
counterparts
due
improved
mass
heat
transfer,
offering
a
good
opportunity
for
industrial
application.
Herein,
rapid
Simmons‐Smith
cyclopropanation
process
is
presented.
Taking
advantage
in
situ
production
zinc
carbenoid
species,
several
olefins
bearing
aromatic
rings
different
electronic
nature,
aliphatic
chains
or
heterocycles
were
smoothly
cyclopropanated
with
residence
time
just
15
minutes.
In
addition,
applicability
protocol
assured
successful
12‐mmol
scale
experiment,
which
represents
3.59
grams
per
hour
selected
example,
satisfactory
synthesis
pharmaceutical
drugs.
Language: Английский
Sulfur Tetrafluoride (SF4) as a Deoxyfluorination Reagent for Organic Synthesis in Continuous Flow Mode
Dominik Polterauer,
No information about this author
Paul Hanselmann,
No information about this author
Ryan Littich
No information about this author
et al.
Organic Process Research & Development,
Journal Year:
2023,
Volume and Issue:
27(12), P. 2385 - 2392
Published: Nov. 24, 2023
We
report
the
development
of
a
deoxyfluorination
protocol
using
sulfur
tetrafluoride
(SF4)
as
reagent
to
prepare
organofluorine
compounds
in
continuous
flow
mode.
The
method
uses
mild
conditions,
without
use
HF,
which
provides
an
improved
safety
profile.
methodology
was
applied
successfully
convert
various
alcohols,
aldehydes,
and
carboxylic
acids
their
corresponding
fluorinated
compounds.
Advantages
include
tolerance
protecting
groups,
high
enantioselective
control,
easy
incorporation
inline
reaction
monitoring.
Language: Английский
Advances in Continuous Flow Fluorination Reactions
Tsz Chun Lee,
No information about this author
Yi Tong,
No information about this author
Wai Chung Fu
No information about this author
et al.
Chemistry - An Asian Journal,
Journal Year:
2023,
Volume and Issue:
18(21)
Published: Sept. 14, 2023
Fluorination
reactions
are
important
in
constructing
organofluorine
motifs,
which
contribute
to
favorable
biological
properties
pharmaceuticals
and
agrochemicals.
However,
fluorination
reagents
associated
with
various
problems,
such
as
their
hazardous
nature,
high
exothermicity,
poor
selectivity
scalability.
Continuous
flow
has
emerged
a
transformative
technology
provide
many
advantages
relative
batch
syntheses.
This
review
article
summarizes
recent
continuous
techniques
that
address
the
limitations
challenges
of
reactions.
Approaches
based
on
different
discussed,
including
gas-liquid
reactions,
packed-bed
reactors,
in-line
purifications,
streamlined
multistep
synthesis,
large-scale
well
photoredox-
electrocatalysis.
Language: Английский
Development of an Optimized Process for 2,4-Dichloro-5-fluoroacetophenone: A Key Intermediate of Ciprofloxacin
Kai Yin,
No information about this author
Youlan He,
No information about this author
Hao Wu
No information about this author
et al.
Organic Process Research & Development,
Journal Year:
2024,
Volume and Issue:
28(8), P. 3284 - 3294
Published: July 24, 2024
Herein,
we
report
an
optimized
process
for
2,4-dichloro-5-fluoroacetophenone,
a
key
intermediate
of
ciprofloxacin.
In
the
nitration
step,
traditional
mixed
acid
was
replaced
by
microchannel
continuous
reaction
technology.
For
fluorination
reactions,
quaternary
ammonium
salt
catalyst
novel
CNC+
catalyst,
which
led
to
improved
catalytic
efficiency,
lowered
temperatures,
and
increased
product
yields.
Furthermore,
cost-effective
method
utilizing
waste
gases
with
high
concentrations
nitrogen
oxides
developed
nitrochlorination
reaction.
acetylation
magnetic
materials
featuring
both
Bronsted
Lewis
sites
were
utilized
immobilize
bisacid
site
[HPhIm][FeCl4]/MPNs,
replacing
AlCl3
approach.
The
overall
yield
this
new
sustainable
across
all
four
steps
reached
86.4%,
marking
significant
improvement
over
10%
compared
method.
Moreover,
has
resulted
in
87%
reduction
emissions
remarkable
96%
exhaust
emissions.
Language: Английский
Recent advances in fluorine chemistry using flow technology
Journal of Fluorine Chemistry,
Journal Year:
2024,
Volume and Issue:
279, P. 110349 - 110349
Published: Sept. 14, 2024
Language: Английский
Fully Continuous Flow Synthesis of 2′-Deoxy-2′-fluoro-arabinoside: A Key Intermediate of Azvudine
Yan Chen,
No information about this author
Yongcheng Sun,
No information about this author
Yufang Xu
No information about this author
et al.
Organic Process Research & Development,
Journal Year:
2024,
Volume and Issue:
28(8), P. 3273 - 3283
Published: July 31, 2024
Azvudine
was
approved
for
the
treatment
of
adult
HIV-1
infection
in
China
2021,
and
it
conditional
marketing
SARS-CoV-2
2022.
In
this
work,
we
describe
a
fully
continuous
flow
synthesis
2′-deoxy-2′-fluoroarabinoside,
key
intermediate
azvudine.
The
process
accomplished
via
six
chemical
transformations,
including
chlorination,
hydrolysis,
fluorination,
bromination,
condensation,
deprotection
sequential
devices.
Under
optimized
conditions,
total
yield
32.3%
with
residence
time
156
min.
Compared
batch
doubled,
reaction
shortened
16
times,
E
factor
reduced
1.63
times.
Language: Английский
Continuous flow synthesis of alkynes from isoxazolones
Aisling Loftus,
No information about this author
Rosa De Gregorio,
No information about this author
Marcus Baumann
No information about this author
et al.
Organic & Biomolecular Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 20, 2024
We
present
an
efficient
flow
method
for
the
preparation
of
disubstituted
alkynes
from
isoxazolones
under
diazotisation
conditions.
This
overcomes
reproducibility
issues
batch
variant
and
safely
affords
alkyne
products
on
gram
scale.
Language: Английский