Nickel-catalyzed hydroarylation reaction: a useful tool in organic synthesis
Sayantika Bhakta,
No information about this author
Tapas Ghosh
No information about this author
Organic Chemistry Frontiers,
Journal Year:
2022,
Volume and Issue:
9(18), P. 5074 - 5103
Published: Jan. 1, 2022
The
nickel-catalyzed
hydroarylation
reaction
opens
up
new
routes
to
access
complex
organic
compounds
in
a
highly
regio
and
stereoselective
fashion
from
easily
available
precursors,
such
as
olefin,
alkyne,
arene,
aryl
halide,
boronic
acid.
Language: Английский
Base‐catalyzed Effective C2‐Amidation of Azolium Salts Using Isocyanates under Mild Conditions
Somnath Bauri,
No information about this author
Arya Ramachandran,
No information about this author
Arnab Rit
No information about this author
et al.
Chemistry - An Asian Journal,
Journal Year:
2023,
Volume and Issue:
18(7)
Published: Feb. 27, 2023
An
unprecedented
base-catalyzed
hydroarylation
of
isocyanates
with
azolium
salts
was
developed,
which
follows
a
simple
reaction
pathway
and
provided
facile
access
to
diverse
C2-amidated
under
mild
conditions.
Importantly,
this
methodology
can
also
be
applied
for
the
successive
C2-amidation
bisimidazolium
salt
two
different
provide
corresponding
unsymmetrically
substituted
bisamide
derivatives.
Notably,
obtained
amidated
serve
as
prominent
carbene
surrogate
synthesis
metal-NHC
complexes.
Language: Английский
CpXCo(III)‐catalyzed selective C–H alkenylation of indoles with ethynylethylene carbonates
Applied Organometallic Chemistry,
Journal Year:
2022,
Volume and Issue:
36(11)
Published: Aug. 16, 2022
An
efficient
and
selective
insertion
of
indoles
into
ethynylethylene
carbonates
has
been
achieved
via
Cp
X
Co(III)‐catalyzed
C–H
functionalization.
Compared
with
a
Cp*Co(III)
catalyst,
the
more
sterically
hindered
Co(III)
improved
selectivity
rare
1,2‐insertion.
This
protocol
provides
an
approach
for
synthesizing
various
vinylindoles
in
good
yields
high
regioselectivity.
Language: Английский