Synthesis of meta-Sulfonylpyridines via Copper(II)-Catalyzed Cascade Sulfonylation/Cyclization/Aromatization of Tertiary Enamides with Sulfonylhydrazides
The Journal of Organic Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 5, 2025
A
copper(II)-catalyzed
radical
cascade
reaction
of
N-propargyl
enamides
with
sulfonyl
hydrazides
was
developed,
which
provided
an
unprecedented
method
for
the
direct
synthesis
meta-sulfonylpyridines
in
high
efficiency
good
functional
group
compatibility
and
simple
operation.
Mechanistic
studies
indicated
that
this
tandem
process
might
be
composed
addition,
intramolecular
cyclization
oxidative
aromatization.
Language: Английский
Alkene 1,3‐Difluorination via Transient Oxonium Intermediates
Alice C. Dean,
No information about this author
E. Harvey Randle,
No information about this author
Andrew J. D. Lacey
No information about this author
et al.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(30)
Published: May 2, 2024
Abstract
The
1,3‐difunctionalization
of
unactivated
alkenes
is
an
under‐explored
transformation
that
leads
to
moieties
are
otherwise
challenging
prepare.
Herein,
we
report
a
hypervalent
iodine‐mediated
1,3‐difluorination
homoallylic
(aryl)
ethers
give
unreported
1,3‐difluoro‐4‐oxy
groups
with
moderate
excellent
diastereoselectivity.
proceeds
through
different
mode
reactivity
for
1,3‐difunctionalization,
in
which
regioselective
addition
fluoride
opens
transiently
formed
oxonium
intermediate
rearrange
alkyl
chain.
optimized
protocol
scalable
and
shown
proceed
well
variety
functional
substitution
on
the
alkenyl
chain,
hence
providing
ready
access
this
fluorinated,
conformationally
controlled
moiety.
Language: Английский
Magnetic studies and Hirshfeld surface analysis of acetato bridged 2D Mn(II) coordination polymer with 4-aminobenzohydrazide ligand
Polyhedron,
Journal Year:
2024,
Volume and Issue:
264, P. 117207 - 117207
Published: Aug. 30, 2024
Language: Английский
Alkene 1,3‐Difluorination via Transient Oxonium Intermediates
Alice C. Dean,
No information about this author
E. Harvey Randle,
No information about this author
Andrew J. D. Lacey
No information about this author
et al.
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(30)
Published: May 2, 2024
Abstract
The
1,3‐difunctionalization
of
unactivated
alkenes
is
an
under‐explored
transformation
that
leads
to
moieties
are
otherwise
challenging
prepare.
Herein,
we
report
a
hypervalent
iodine‐mediated
1,3‐difluorination
homoallylic
(aryl)
ethers
give
unreported
1,3‐difluoro‐4‐oxy
groups
with
moderate
excellent
diastereoselectivity.
proceeds
through
different
mode
reactivity
for
1,3‐difunctionalization,
in
which
regioselective
addition
fluoride
opens
transiently
formed
oxonium
intermediate
rearrange
alkyl
chain.
optimized
protocol
scalable
and
shown
proceed
well
variety
functional
substitution
on
the
alkenyl
chain,
hence
providing
ready
access
this
fluorinated,
conformationally
controlled
moiety.
Language: Английский
Synthesis of Γ-Keto Sulfones Through Sulfonylation/Acylation of Alkenes Merging Nhc- and Photo-Catalysis
Jie Liu,
No information about this author
Xu Sun,
No information about this author
Gan Zhang
No information about this author
et al.
Published: Jan. 1, 2024
Language: Английский
Synthesis of γ-keto sulfones through sulfonylation/acylation of alkenes merging NHC- and photo-catalysis
Xu Sun,
No information about this author
Gan Zhang,
No information about this author
Bo Ye
No information about this author
et al.
Molecular Catalysis,
Journal Year:
2024,
Volume and Issue:
569, P. 114563 - 114563
Published: Sept. 25, 2024
Language: Английский
Paired Electrocatalysis-Enabled Cross Coupling of Sulfinamides with Olefins toward the Synthesis of Vinyl Sulfoximines
Tao Liu,
No information about this author
Yan Tang,
No information about this author
Jiyuan Guo
No information about this author
et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(40), P. 8463 - 8467
Published: Oct. 2, 2024
We
present
here
a
novel
paired
electrocatalysis-enabled
convenient
synthesis
of
the
(
Language: Английский
Synthesis of Alkyl Sulfones via a Photocatalytic Multicomponent Reaction of Aryldiazo Tetrafluoroborate Salts, Styrene Derivatives, and Sodium Metabisulfite
Organic & Biomolecular Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 25, 2024
Practical
visible-light-induced
synthesis
of
alkyl
sulfones
has
been
achieved
via
a
multicomponent
reaction
aryldiazo
tetrafluoroborate
salts,
styrene
derivatives,
thiophenol
and
sodium
metabisulfite
in
the
presence
rhodamine
B.
Language: Английский