Advanced Synthesis & Catalysis,
Год журнала:
2022,
Номер
364(21), С. 3657 - 3663
Опубликована: Сен. 21, 2022
Abstract
A
strategy
for
the
divergent
synthesis
of
polysubstituted
pyrazoles
and
N
‐alkylated
hydrazone
derivatives
through
three‐component
reaction
aromatic
aldehydes,
aryl
sulfonyl
hydrazides,
allenoates
under
mild
conditions
is
described.
Both
products
can
be
obtained
by
changing
base.
magnified
image
The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
89(15), С. 10816 - 10830
Опубликована: Июль 15, 2024
Dearomative
annulation
reaction
of
acyl-tethered
benzothiazole
bisnucleophiles
with
β'-acetoxy
allenoates
by
switching
the
Lewis
base
is
developed.
The
DBU-catalyzed
gives
benzothiazole-fused
1,4-dihydropyridine
carboxylates
(3
+
3)
chemoselectively.
By
contrast,
PR
The Journal of Organic Chemistry,
Год журнала:
2022,
Номер
87(9), С. 6362 - 6370
Опубликована: Апрель 15, 2022
Herein,
we
describe
a
DABCO-catalyzed
[4
+
2]
annulation
between
5-methylenehex-2-ynedioates
and
electron-deficient
olefins
to
afford
functionalized
cyclohexadienes
in
good
yields
under
mild
conditions.
The
use
of
β-
ε-carbons
the
substrates
for
C-C
bond
formation
is
distinct
from
previous
reports
showing
substrate-controlled
divergent
reactivity.
believed
proceed
domino
cyclization
initiated
by
cross
Rauhut-Currier
reaction.
Advanced Synthesis & Catalysis,
Год журнала:
2022,
Номер
364(21), С. 3657 - 3663
Опубликована: Сен. 21, 2022
Abstract
A
strategy
for
the
divergent
synthesis
of
polysubstituted
pyrazoles
and
N
‐alkylated
hydrazone
derivatives
through
three‐component
reaction
aromatic
aldehydes,
aryl
sulfonyl
hydrazides,
allenoates
under
mild
conditions
is
described.
Both
products
can
be
obtained
by
changing
base.
magnified
image