Nickel‐Catalyzed Asymmetric Reductive 1,4‐ and 1,5‐Dicarbofunctionalization†
Yutong Xiang,
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Chang Zhang,
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Chuan Wang
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et al.
Chinese Journal of Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 8, 2025
Comprehensive
Summary
Herein,
we
present
the
first
examples
of
asymmetric
reductive
1,4‐dicarbofunctionalization
1,3‐dienes
and
1,5‐dicarbofunctionalization
vinylcyclopropanes,
which
proceed
under
catalysis
a
chiral
nickel/bis‐imidazoline
complex
using
alkyl
halides
aryl
iodides
or
alkenyl
bromides
as
electrophilic
coupling
partners.
In
these
highly
enantioselective
transformations
operating
in
radical
relay
mechanism,
C(sp
3
)‐
2
)‐type
carbo‐moieties
are
respectively
installed
on
terminal
internal
position
with
newly
formed
olefinic
unit
high
E
‐selectivity.
Language: Английский
Electrochemical 1,5-chlorosulfonylation and 1,5-hydrosulfonylation of vinylcyclopropanes
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(19), P. 5564 - 5572
Published: Jan. 1, 2024
This
study
reports
the
electrochemical
reaction
of
vinylcyclopropanes
with
sulfonyl
chlorides,
resulting
in
1,5-hydrosulfonylation
and
1,5-chlorosulfonylation.
Language: Английский
Access to Vinyl gem‐Difluorinated Cyclopropanes via Photopromoted Palladium‐Catalyzed Heck Reaction
Bin Li,
No information about this author
Quanxiang Feng,
No information about this author
Jingjing Yuan
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et al.
Chemistry - An Asian Journal,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 18, 2024
Abstract
A
photopromoted
Pd‐catalyzed
Heck
reaction
of
gem
‐difluorocyclopropyl
bromides
(DFCBs)
with
styrenes
to
deliver
vinyl
‐difluorinated
cyclopropanes
(VDFCs)
under
mild
conditions
has
been
developed.
The
demonstrates
good
functional
group
compatibility
while
providing
high
E/Z
ratio
the
products.
Furthermore,
desired
VDFCs
can
be
easily
transformed
into
fluorinated
cyclic/acyclic
architectures,
which
may
broaden
its
applications
in
organic
synthesis.
Language: Английский
Photocatalytic 1,3-Oxyheteroarylation of Aryl Cyclopropanes with Azine N-oxides
Chemical Science,
Journal Year:
2024,
Volume and Issue:
15(48), P. 20433 - 20439
Published: Jan. 1, 2024
Developed
a
difunctionalization
method
for
aryl
cyclopropanes
using
azine
N
-oxides
as
bifunctional
reagents,
generating
β-heteroaryl
ketones.
This
enables
the
use
of
previously
challenging
electron-deficient
cyclopropanes.
Language: Английский