Green Chemistry,
Год журнала:
2022,
Номер
24(3), С. 1342 - 1349
Опубликована: Янв. 1, 2022
Electrocatalysis
for
the
controllable
coupling
of
thiols
with
DCE
was
achieved
to
generate
value-added
β-chloro-tethered
sulfur
compounds
in
batch
and
flow.
Green Chemistry,
Год журнала:
2021,
Номер
23(11), С. 3950 - 3954
Опубликована: Янв. 1, 2021
An
electrochemical
multicomponent
reaction
was
established
under
catalyst-,
chemical-oxidant-free
and
mild
conditions,
which
provides
an
eco-friendly
simple
protocol
for
constructing
4-selanylpyrazoles
from
easily
available
raw
materials
with
high
yields.
Green Synthesis and Catalysis,
Год журнала:
2021,
Номер
2(1), С. 19 - 26
Опубликована: Фев. 1, 2021
As
one
of
the
most
important
biogeochemical
cycles,
carbon
dioxide
(CO2)
cycle
between
atmosphere
and
biosphere
has
a
profound
impact
on
life
earth.
Therefore,
search
for
sustainable
solutions
to
normalize
currently
unbalanced
is
central
research
topic
many
scientific
disciplines.
The
green
electrocatalysis
offers
very
promising
answer
cycle.
In
this
review,
recent
advances
in
enabled
CO2
including
electrochemical
carboxylation
decarboxylative
functionalization
carboxylic
acids
are
highlighted.
Chemical Communications,
Год журнала:
2023,
Номер
59(36), С. 5343 - 5364
Опубликована: Янв. 1, 2023
The
activation
and
transformation
of
organic
chemical
bonds
is
a
fundamental
scientific
problem.
In
the
past
several
decades,
C-S
bond
cleavage
for
construction
C-C
C-heteroatom
has
received
tremendous
attention
in
chemistry.
Although
significant
progress
been
made
field
transition
metal
strategies,
variety
novel
transition-metal-free
strategies
have
also
developed
using
halogenated
reagents,
oxidants,
acids,
bases.
Moreover,
photochemical
electrochemical
methods
to
achieve
organosulfur
compounds.
To
date,
however,
no
comprehensive
review
reported.
Therefore,
we
herein
provide
major
advances
compounds,
including
thioethers,
sulfoxides,
sulfones,
thioacetals,
sulfonium
salts,
sulfur
ylides.
Angewandte Chemie International Edition,
Год журнала:
2021,
Номер
60(17), С. 9362 - 9367
Опубликована: Фев. 4, 2021
Abstract
A
catalytic
atroposelective
cycloaddition
reaction
between
thioureas
and
ynals
is
developed.
This
features
the
first
NHC‐catalyzed
addition
of
to
acetylenic
acylazolium
intermediates
eventually
set
up
C−N
axial
chirality
with
excellent
optical
purities.
The
obtained
axially
chiral
thiazine
derivative
products
bear
multiple
functional
groups
are
feasible
for
further
transformations.
Green Synthesis and Catalysis,
Год журнала:
2021,
Номер
2(1), С. 45 - 53
Опубликована: Янв. 27, 2021
Regioselective
syntheses
of
glycosides
using
modern
chemical
methods
suffer
from
the
need
to
invoke
multiple
steps
protection
and
deprotection,
even
then
product
mixtures
may
occur.
Discovering
tuning
by
mutagenesis
glycosyltransferases
(GTs)
with
considerable
substrate
promiscuity
is
an
alternative
challenge.
We
tuned
rational
design
based
on
extended
Focused
Rational
Iterative
Site-specific
Mutagenesis
(FRISM)
a
newly
identified
GT
Siraitia
grosvenorii
(UGT74AC2)
as
catalyst
in
targeted
regioselective
glucosylation
polyhydroxy
silybin
derivatives.
A
handful
mutants
was
constructed
restricted
set
rationally
chosen
amino
acids,
providing
variants
showing
94%,
>
99%
selectivity
3-OH,
7-OH
3,7-O-diglycoside,
respectively,
compared
wildtype
resulting
22%:39%:39%
mixture.
Remarkably,
N-
S-glucosylation
achieved.
Docking
molecular
dynamics
(MD)
simulations
studies
shed
light
origin
regioselectivity.
These
findings
can
be
invoked
guide
future
enzymatic
tailoring
UGTs
production
flavonoids
potent
pharmaceuticals
other
useful
compounds.
Green Synthesis and Catalysis,
Год журнала:
2021,
Номер
2(3), С. 247 - 266
Опубликована: Май 7, 2021
Hydroformylation
of
olefins
can
generate
linear
and
branched
aldehydes,
the
aldehydes
are
attractive
precursors
for
synthesis
fine
chemicals
pharmaceuticals.
is
considered
an
important
strategy
green
chemistry
because
its
intrinsic
atom
economic
nature
recent
development
highly
selective
protocols.
We
herein
summarize
advances
hydroformylation
showing
selectivity
in
organic
synthesis.
A
mechanistic
discussion
provided
prior
to
examples
synthetically
useful
branch-selective
reactions.
Branch-selective
further
contribute
construction
chiral
molecules
design
one-pot
This
review
aims
provide
information
about
catalyst
selection,
reaction
conditions,
substrate
scope
hydroformylation,
inspire
this
chemistry.