Highly dispersed ruthenium capsulated in UiO-66-NH2 for hydrogen-borrowing-mediated N-alkylation reactions
Jiahao Li,
No information about this author
Shiguo Ou,
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Xinxin Sang
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et al.
Catalysis Science & Technology,
Journal Year:
2024,
Volume and Issue:
14(7), P. 1958 - 1966
Published: Jan. 1, 2024
Herein,
atomically
dispersed
Ru
sites
are
encapsulated
within
UiO-66–NH
2
frameworks
to
serve
as
a
highly
active,
selective,
and
stable
catalyst
for
amine
synthesis
via
N
-alkylation
reactions
of
o
-phenylenediamine
with
monohydric
alcohols.
Language: Английский
Temperature-dependent switchable synthesis of imines and amines via coupling of alcohols and amines using pyrrolyl-imine ruthenium catalysts
Qing Li,
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Yu Hou,
No information about this author
Mengxuan Bai
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et al.
Journal of Catalysis,
Journal Year:
2024,
Volume and Issue:
unknown, P. 115895 - 115895
Published: Dec. 1, 2024
Language: Английский
N-Heterocyclic carbene supported zinc catalysed N-formylation of diverse N–H functionalities with carbon dioxide under ambient conditions
Sangita Sahoo,
No information about this author
Subarna Manna,
No information about this author
Arnab Rit
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et al.
Catalysis Science & Technology,
Journal Year:
2023,
Volume and Issue:
13(11), P. 3344 - 3350
Published: Jan. 1, 2023
A
heteroditopic
NHC
ligand
supported
Zn-catalysed
RT
N
-formylation
of
diverse
N–H
moieties
with
CO
2
(1
bar)
using
PhSiH
3
was
developed,
which
offers
excellent
functional
group
tolerance,
chemoselectivity,
and
synthons
for
biologically
relevant
compounds.
Language: Английский
Control over borrowing hydrogen and acceptorless dehydrogenative coupling process for the Co(iii)–NHC catalysed chemoselective alkylation and cyclisation of 1,2-phenylenediamine with alcohols
Misba Siddique,
No information about this author
Biswaranjan Boity,
No information about this author
Arnab Rit
No information about this author
et al.
Catalysis Science & Technology,
Journal Year:
2023,
Volume and Issue:
13(24), P. 7172 - 7180
Published: Jan. 1, 2023
Chemoselective
alkylation
and
cyclisation
of
1,2-phenylenediamine
with
alcohols
via
control
cobalt–NHC
catalysed
borrowing
hydrogen
acceptorless
dehydrogenative
coupling
is
achieved
by
tuning
the
triazole
substituent
NHC
ligand
system.
Language: Английский
Heteroditopic NHC Ligand Supported Manganese(I) Complexes: Synthesis, Characterization, and Activity as Non‐bifunctional Phosphine‐Free Catalyst for the α‐Alkylation of Nitriles
Chemistry - A European Journal,
Journal Year:
2023,
Volume and Issue:
30(1)
Published: Oct. 9, 2023
Abstract
In
the
present
work,
several
manganese(I)
complexes
of
chelating
heteroditopic
ligands
Mn1–3
,
featuring
ImNHC
(imidazol‐2‐ylidene)
connected
to
a
1,2,3‐triazole‐N
or
tzNHC
(1,2,3‐triazol‐5‐ylidene)
donors
via
methylene
spacer,
with
possible
modifications
at
triazole
backbone
have
been
synthesized
and
completely
characterized.
Notably,
CO
stretching
frequencies,
electrochemical
analysis,
frontier
orbital
analysis
certainly
suggest
that
ImNHC‐tzNHC
stronger
donation
capabilities
than
related
ImNHC‐Ntz
ligand
in
complexes.
Moreover,
these
well‐defined
phosphine‐free
Mn(I)−NHC
found
be
effective
non‐bifunctional
catalysts
for
α‐alkylation
nitriles
using
alcohols
importantly,
catalyst
Mn1
containing
weaker
triazole‐N
donor
displayed
higher
activity
compared
Mn2
/
Mn3
an
unsymmetrical
bis‐carbene
(ImNHC
tzNHC).
A
wide
range
aryl
were
coupled
diverse
(hetero)aromatic
as
well
aliphatic
get
corresponding
products
good
excellent
yields
(32
examples,
up
95
%
yield).
The
detailed
mechanistic
studies
including
deuterium
labelling
experiments
reveal
reaction
follows
Borrowing
Hydrogen
pathway.
Language: Английский
Development of a Mild and Efficient Process for Ir-Catalyzed N-Alkylation of 4-Bromopyridin-2-amine with a Primary Alcohol via Borrowing Hydrogen
Organic Process Research & Development,
Journal Year:
2024,
Volume and Issue:
28(8), P. 3414 - 3422
Published: July 25, 2024
We
report
herein
the
development
and
scale
up
of
an
Ir-catalyzed
N-alkylation
reaction
between
a
4-bromopyridin-2-amine
(1)
(4-(5-(1,1-difluoroethyl)-1,2,4-oxadiazol-3-yl)bicyclo[2.2.2]octan-1-yl)methanol
(2)
proceeding
via
borrowing
hydrogen
process.
The
traditional
approach
alcohol
oxidation
followed
by
reductive
amination
posed
challenges
that
are
attributed
to
poor
nucleophilicity
2-aminopyridine
derivative
resulting
in
lower
isolated
yields.
Several
catalysts
bases
were
evaluated
for
successful
1
with
2,
Ir
(III)
catalyst
combination
LiOt-Bu
as
base
was
found
provide
optimal
conversion.
process
successfully
demonstrated
on
1.5
kg
afforded
>70%
yield
3
without
need
sealed
reactor
or
any
other
specialized
equipment.
Language: Английский
Construction of C–X (X = N, O) bonds from benzyl alcohols via Cu-BTC-catalyzed oxidative coupling
Yujuan Wu,
No information about this author
Lianji Zhang,
No information about this author
Huimin Liu
No information about this author
et al.
Catalysis Science & Technology,
Journal Year:
2024,
Volume and Issue:
14(15), P. 4366 - 4375
Published: Jan. 1, 2024
Herein,
an
efficient
and
environmentally
friendly
Cu-BTC
catalytic
system
is
reported,
which
can
be
successfully
applied
to
the
oxidative
coupling
of
benzyl
alcohols
for
construction
C–X
(X
=
N,
O)
bonds.
Language: Английский
An efficient heterogeneous copper oxide nanocatalyst for N-alkylation of amines with carbonyl compounds under H2 atmosphere
M. Sharath Babu,
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N. Padmaja,
No information about this author
G. Bhagavanth Reddy
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et al.
Results in Chemistry,
Journal Year:
2023,
Volume and Issue:
5, P. 100947 - 100947
Published: Jan. 1, 2023
The
aim
of
this
research
is
to
investigate
the
potential
copper
oxide
nanoparticles
(CuO
NPs)
as
a
catalyst
for
reductive
N-alkylation
amines
with
carbonyl
compounds
in
order
synthesize
secondary
an
H2
environment.
synthesized
CuO
NPs
were
characterized
using
UV–vis
DRS,
XRD,
FT-IR,
and
TEM
techniques,
which
confirmed
their
spherical
shape,
monoclinic
phase,
average
diameter
9
±
2
nm.
results
catalytic
study
indicate
that
was
able
produce
various
excellent
yield.
also
explored
effects
reaction
time,
temperature,
weight
under
optimum
conditions.
Additionally,
shown
be
highly
stable
could
reused
three
cycles
without
any
loss
activity
formation
amines.
Language: Английский