Ru(II)‐Catalyzed Selective C—H Alkynylation of Isoquinolones, Quinazolones and Phthalazinones with Bromoalkynes
Chinese Journal of Chemistry,
Год журнала:
2024,
Номер
42(15), С. 1686 - 1690
Опубликована: Март 15, 2024
Comprehensive
Summary
A
new,
selective
Ru(II)‐catalyzed
alkynylation
reaction
of
isoquinolones,
quinazolones
and
phthalazinones
with
readily
available
bromoalkynes
has
been
developed.
This
enables
the
construction
a
new
C(sp
2
)‐C(sp)
bond
through
C—H
activation
C—Br
functionalization,
offers
an
effective
route
to
synthesizing
highly
valuable
alkynylated
isoquinolone,
quinazolone
phthalazinone
derivatives
wide
substrate
scope
high
selectivity.
Язык: Английский
Rh-Catalyzed C–H Alkynylation of Indole Derivatives with Silver(I)-Controlled Regiodivergence
Yaokun Zhao,
Xingchi Li,
Pengfei Zhou
и другие.
Organic Letters,
Год журнала:
2024,
Номер
26(35), С. 7285 - 7290
Опубликована: Авг. 23, 2024
We
have
disclosed
silver(I)-induced
switching
of
regioselectivity
in
rhodium-catalyzed
C–H
alkynylation
indole
derivatives
with
the
help
a
pivaloyl
directing
group
by
tuning
metalation
modes.
The
judicious
choice
AgOAc,
Ag2O,
and
Ag2CO3
affords
an
array
C2-alkynylated
indoles,
C4-alkynylated
C2,C4-dialkynylated
respectively.
synthetic
utility
alkyne
fragment
is
demonstrated
derivatization
into
valuable
indole-based
compounds.
Язык: Английский
Isoxazole group directed Rh(III)-catalyzed alkynylation using TIPS-EBX
Organic & Biomolecular Chemistry,
Год журнала:
2024,
Номер
22(34), С. 6922 - 6927
Опубликована: Янв. 1, 2024
A
highly
effective
isoxazole
directed
Язык: Английский
Ruthenium(II)‐Catalyzed Selective C(sp2)−H Acyloxylation of 2‐Aroyl‐Pyridine Derivatives with Sodium Carboxylate
Advanced Synthesis & Catalysis,
Год журнала:
2023,
Номер
366(3), С. 518 - 525
Опубликована: Дек. 29, 2023
Abstract
A
ruthenium‐catalyzed
C(
sp
2
)−H
acyloxylation
of
2‐aroyl
pyridine
derivatives
with
simple
sodium
carboxylate
utilizing
transformable
directing
groups
is
described.
This
protocol
features
broad
functional
group
tolerance
and
chemo‐
regio‐selectivity,
providing
the
products
in
45%‐84%yield.
Furthermore,
synthetic
utility
this
was
demonstrated
by
late‐stage
functionalization
pharmaceutical
compounds.
Notably,
could
be
further
transformed
into
a
variety
useful
heterocycles
under
mild
conditions.
Язык: Английский