Organic Chemistry Frontiers,
Journal Year:
2021,
Volume and Issue:
8(24), P. 6874 - 6880
Published: Jan. 1, 2021
An
asymmetric
tandem
cycloisomerization/[3
+
2]
cycloaddition
reaction
of
2,2′-diester
aziridine
and
2-ethynyl
benzyl
alcohol
with
Au(
i
)/chiral
N
,
′-dioxide−Dy(
iii
)
as
a
relay
catalyst
system
was
developed.
Organic Letters,
Journal Year:
2021,
Volume and Issue:
23(8), P. 2954 - 2958
Published: March 26, 2021
A
highly
enantioselective
three-component
reaction
of
ynamides
with
carboxylic
acids
and
2,2′-diester
aziridines
has
been
realized
by
using
a
chiral
N,N′-dioxide/Ho(OTf)3
complex
as
Lewis
acid
catalyst.
The
process
includes
the
formation
an
α-acyloxyenamide
intermediate
through
addition
to
following
nucleophilic
in-situ-generated
azomethine
ylides
induced
range
amino
acyloxyenamides
are
delivered
in
moderate
good
yields
ee
values.
In
addition,
possible
catalytic
cycle
transition
model
is
proposed
elucidate
mechanism.
Organic Chemistry Frontiers,
Journal Year:
2022,
Volume and Issue:
9(17), P. 4591 - 4597
Published: Jan. 1, 2022
An
asymmetric
cascade
reaction
catalyzed
by
a
chiral
N
,
′-dioxide–Dy(
iii
)
complex
was
realized
to
construct
the
valuable
[6,5,5,6]
tetracyclic
spiroindolines
with
good
yields
and
enantioselectivities
concise
one-step
protocol.
Organic & Biomolecular Chemistry,
Journal Year:
2022,
Volume and Issue:
20(6), P. 1219 - 1225
Published: Jan. 1, 2022
A
facile
NHC-catalyzed
[2
+
4]
annulation
of
allenoates
with
2,3-dioxypyrrolidine
derivatives
was
discovered,
which
paved
a
new
avenue
for
the
construction
highly
substituted
pyranopyrrole
moderate
to
good
yields,
high
atom
economy
and
mild
reaction
conditions.
Organic Chemistry Frontiers,
Journal Year:
2021,
Volume and Issue:
8(24), P. 6874 - 6880
Published: Jan. 1, 2021
An
asymmetric
tandem
cycloisomerization/[3
+
2]
cycloaddition
reaction
of
2,2′-diester
aziridine
and
2-ethynyl
benzyl
alcohol
with
Au(
i
)/chiral
N
,
′-dioxide−Dy(
iii
)
as
a
relay
catalyst
system
was
developed.