Chemical Science,
Год журнала:
2022,
Номер
13(14), С. 4103 - 4108
Опубликована: Янв. 1, 2022
An
asymmetric
[1,2]
Stevens
rearrangement
was
realized
via
chiral
guanidine
and
copper(
i
)
complexes.
A
series
of
novel
dithioketal
derivatives
were
obtained
with
good
yields
(up
to
90%
yield)
enantioselectivities
96
:
4
er).
Natural Product Reports,
Год журнала:
2020,
Номер
38(3), С. 586 - 667
Опубликована: Окт. 6, 2020
Covering:
2017-2019Guanidine
natural
products
isolated
from
microorganisms,
marine
invertebrates
and
terrestrial
plants,
amphibians
spiders,
represented
by
non-ribosomal
peptides,
guanidine-bearing
polyketides,
alkaloids,
terpenoids
shikimic
acid
derived,
are
the
subject
of
this
review.
The
topics
include
discovery
new
metabolites,
total
synthesis
guanidine
compounds,
biological
activity
mechanism-of-action,
biosynthesis
ecological
functions.
ACS Catalysis,
Год журнала:
2021,
Номер
11(10), С. 6316 - 6324
Опубликована: Май 11, 2021
Chiral
N-heterocyclic
carbenes
(NHCs)
have
been
recently
established
as
powerful
catalysts
for
enantioselective
bond-forming
processes
via
noncovalent
interactions.
The
underlying
HOMO-raising
activation
of
nucleophiles
takes
advantage
the
strong
Brønsted
basicity
NHCs.
However,
scope
compatible
electrophiles
has
quite
limited.
In
this
article,
we
report
a
bifunctional
NHC
with
an
embedded
hydrogen-bonding
motif
that
shows
remarkable
tolerance
various
Michael
acceptors
in
asymmetric
aza-conjugate
addition
reaction.
catalytic
efficiency
far
exceeds
benchmark
tertiary
amine-thiourea
scaffold.
Dalton Transactions,
Год журнала:
2022,
Номер
51(6), С. 2567 - 2576
Опубликована: Янв. 1, 2022
The
development
of
heterogeneous
catalysts
for
promoting
epoxide
cycloaddition
with
carbon
dioxide
is
highly
desirable
recycling
CO2
and
achieving
the
goal
neutrality.
Herein,
we
designed
synthesized
Zr-based
metal
organic
frameworks
(MOFs)
by
implanting
functional
guanidyl
into
framework
via
mixing
different
molar
ratios
4-guanidinobenzoic
acid
(Gua)
1,4-benzenedicarboxylic
(BDC).
Consequently,
a
small
sized
Zr-MOF
(∼350
nm)
can
be
prepared
Gua
20%
ligands,
denoted
as
UiO-66-Gua0.2(s).
Compared
to
large
Zr-MOFs,
UiO-66-Gua0.2(s)
exhibited
an
optimal
activity
on
catalyzing
in
presence
Bu4NBr
cocatalyst.
A
yield
97%
product
chloropropene
carbonate
was
achieved
at
90
°C
under
1
atm
CO2.
great
performance
might
attributed
synergistic
effect
groups
hydrogen-bond
donors
Zr
centers
acting
Lewis-acidic
sites.
In
addition,
catalyst
versatility
towards
converting
other
epoxides
satisfactory
recyclability
five
consecutive
runs.
Moreover,
plausible
reaction
mechanism
has
been
proposed
reactions.
European Journal of Organic Chemistry,
Год журнала:
2022,
Номер
26(7)
Опубликована: Дек. 15, 2022
Abstract
Thiourea‐
and
squaramide‐based
bifunctional
base
catalysts
represent
nowadays
a
powerful
tool
in
the
field
of
asymmetric
catalysis
have
demonstrated
very
efficient
for
promoting
wide
variety
transformations
enantioselectively.
New
versions
that
incorporate
one
or
various
additional
H‐bond
donor
site(s)
catalyst
structure
been
developed
recently
which
led
to
more
active
(reduced
loadings)
selective
catalysts.
This
review
highlights
pioneering
ideas
most
recent
contributions
area
with
material
organized
according
nature
functionality.
The
advantages,
current
limitations
perspectives
these
new
multifunctional
are
discussed.
Chemical Science,
Год журнала:
2022,
Номер
13(14), С. 4103 - 4108
Опубликована: Янв. 1, 2022
An
asymmetric
[1,2]
Stevens
rearrangement
was
realized
via
chiral
guanidine
and
copper(
i
)
complexes.
A
series
of
novel
dithioketal
derivatives
were
obtained
with
good
yields
(up
to
90%
yield)
enantioselectivities
96
:
4
er).