Enantioselective functionalization of unactivated C(sp3)–H bonds through copper-catalyzed diyne cyclization by kinetic resolution
Yang‐Bo Chen,
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Li‐Gao Liu,
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Zhe-Qi Wang
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et al.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: March 12, 2024
Site-
and
stereoselective
C-H
functionalization
is
highly
challenging
in
the
synthetic
chemistry
community.
Although
of
vinyl
cations
has
been
vigorously
studied
C(sp
Language: Английский
Dynamic kinetic resolution and dynamic kinetic asymmetric transformation of atropisomeric biaryls
Jie Zhang,
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Xuan-Zhu Huo,
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Yidan Liu
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et al.
Chem Catalysis,
Journal Year:
2025,
Volume and Issue:
unknown, P. 101329 - 101329
Published: March 1, 2025
Language: Английский
Chiral Phosphoric Acid-Catalyzed Kinetic Resolution of Tertiary Alcohol-Tethered Ynamides via Controllable Hydroalkoxylation
Da-Qiu Cui,
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Gan-Lu Qian,
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Hongxing Zheng
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et al.
ACS Catalysis,
Journal Year:
2025,
Volume and Issue:
unknown, P. 2424 - 2433
Published: Jan. 27, 2025
Language: Английский
Modeling and experimental evaluation of biphasic enantioselective liquid-liquid extraction of racemic equol
Zhihong Yan,
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Chenggong Zhou,
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Kexin Zhou
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et al.
Journal of Chromatography A,
Journal Year:
2025,
Volume and Issue:
1748, P. 465844 - 465844
Published: March 5, 2025
Language: Английский
Kinetic Resolution of Sulfoximines via Asymmetric Organocatalyzed Formation of Benzothiadiazine-1-oxides
Mengyao Tang,
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Mengyao Yuan,
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Shibin Hong
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et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(9), P. 1914 - 1919
Published: Feb. 29, 2024
A
catalytic
kinetic
resolution
of
sulfoximines
has
been
developed
through
chiral
phosphoric
acid-catalyzed
intramolecular
dehydrative
cyclizations.
variety
racemic
bearing
an
ortho-amidophenyl
moiety
underwent
asymmetric
cyclizations
using
this
method,
yielding
both
the
recovered
and
benzothiadiazine-1-oxide
products
with
good
to
high
enantioselectivities
(with
s-factor
up
61).
The
diverse
derivatizations
into
a
wide
range
S-stereogenic
center-containing
S,N-heterocycles
have
demonstrated
value
method.
Language: Английский
Kinetic Resolutions Enabled by N-Heterocyclic Carbene Catalysis: An Update
Chinese Journal of Organic Chemistry,
Journal Year:
2024,
Volume and Issue:
44(2), P. 448 - 448
Published: Jan. 1, 2024
Kinetic
resolution
is
one
of
the
most
commonly
used
methods
allowing
access
to
enantioenriched
compounds.The
last
two
decades
have
seen
rapid
development
kinetic
resolutions
enabled
by
N-heterocyclic
carbene
catalysis,
and
part
achievements
been
summarized
in
our
previous
review
paper
published
2017.Since
then,
a
series
new
advances
realized,
this
will
provide
an
update
field
covering
reports
from
mid-2017
2023.
Language: Английский
Kinetic Resolution of P-Chiral Phosphindole Oxides through Rhodium-Catalyzed Asymmetric Arylation
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(18), P. 3987 - 3990
Published: May 1, 2024
Highly
efficient
kinetic
resolution
of
P-chiral
phosphindole
oxides
via
rhodium-catalyzed
asymmetric
arylation
under
mild
conditions
is
described.
Selectivity
factors
up
to
569
were
achieved
by
employing
chiral
diene*
as
a
ligand.
The
transformation
the
enantiopure
benzophosphole
derivative
into
useful
bisphosphine
ligand
also
demonstrated.
Language: Английский
Kinetic resolution of 1,1′-binaphthyl-2,2′-diamine derivatives by chiral calcium phosphate-catalyzed acylation
Tatsuhiro Uchikura,
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Yuki Kanno,
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Yukino Fukuda
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et al.
Organic & Biomolecular Chemistry,
Journal Year:
2024,
Volume and Issue:
22(17), P. 3444 - 3447
Published: Jan. 1, 2024
Chiral
calcium
phosphate-catalyzed
kinetic
resolution
of
BINAM
derivatives.
Language: Английский
Kinetic resolution of 1-(1-alkynyl)cyclopropyl ketones via gold-catalyzed divergent (4 + 4) cycloadditions: stereoselective access to furan fused eight-membered heterocycles
Xunhua Wang,
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Ruifeng Lv,
No information about this author
Xiaoxun Li
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et al.
Chemical Science,
Journal Year:
2024,
Volume and Issue:
15(24), P. 9361 - 9368
Published: Jan. 1, 2024
The
stereoselective
construction
of
furan/pyrrole-fused
eight-membered
heterocycles
via
chiral
gold-catalyzed
(4
+
4)
cycloadditions
was
realized.
Language: Английский