Recent advances in multicomponent synthesis of pyrazoles
Jing Zhou,
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Quan‐Quan Zhou,
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Jie‐Ping Wan
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et al.
Organic & Biomolecular Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
Pyrazole
moiety
is
considered
as
an
important
N-heterocycle
in
pharmaceuticals
and
many
other
functional
molecules.
The
utilization
of
multicomponent
reaction
a
major
tool
the
current
approaches
pyrazole
synthesis.
Considering
power
significance
synthesis,
we
review
herein
latest
developments
this
field.
According
to
typical
features,
contents
are
divided
into
reactions
with
different
NN
fragment
sources,
such
hydrazine,
hydrazone,
amidine,
nitrile,
diazo
compounds,
ring
construction,
covering
works
published
since
2019
date.
Language: Английский
Radical-mediated sulfonylation relay of alkyl alkynes/alkenes and electron-deficient alkenes to access vinyl and alkyl sulfones
Jinhui Liu,
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Fang Long,
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Qing Li
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et al.
Organic Chemistry Frontiers,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
A
radical-mediated
sulfonylation
relay
of
alkyl
alkynes/alkenes
with
electron-deficient
alkenes
using
Na
2
S
O
4
as
a
linker
is
developed
to
synthesize
highly
selective
(
Z
)-vinyl
and
sulfones
under
metal-free
catalyzed
system.
Language: Английский
Regio- and Stereoselective β-Sulfonylamination of Alkynes via Photosensitized Bifunctional N–S Bond Homolysis
Tonglv Pu,
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Si‐Hai Wu,
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Liuyan Cai
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et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 4, 2024
Nitrogen
central
radicals
(NCRs)
are
versatile
synthetic
intermediates
for
creating
functional
nitrogen-containing
molecules.
Herein,
a
photosensitized
β-sulfonylamination
of
terminal
alkynes
as
well
acetylene
has
been
established
by
employing
N-sulfonyl
heteroaromatics
bifunctional
reagents
(BFRs)
to
efficiently
deliver
(E)-β-sulfonylvinylamines
with
excellent
regio-
and
stereoselectivities.
Mechanistic
studies
suggest
base-accelerated
energy
transfer
(EnT)
photocatalysis
involving
aromatic
NCR
formation,
radical
addition
alkynes,
sulfonylation
processes.
Language: Английский
Photoredox/Iron Dual-Catalysis-Enabled [4 + 2] Cyclization of Acyl Nitrene with Alkynes
Shimin Xie,
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Shuwang Tang,
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Ming Hou
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et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 13, 2024
In
this
work,
the
annulation
of
acyl
nitrene
with
alkynes
is
reported
under
photoredox/iron
dual-catalysis
for
synthesis
a
series
isoquninalin-2-ones.
The
reaction
featured
high
regioselectivity
and
good
generality.
particular,
resulting
isoquinalin-2-ones
could
be
structurally
elaborated
into
several
biologically
interesting
scaffolds.
Mechanism
investigation
suggests
that
was
ascribed
to
formal
[4
+
2]
cyclization.
It
believed
represents
an
initial
example
preparing
isoquinolin-1-ones
from
ferric
peroxyl-catalyzed
insertion.
Language: Английский
Sulfonylation/cyclization of alkynes with sulfonyl chlorides by copper catalysis
New Journal of Chemistry,
Journal Year:
2024,
Volume and Issue:
48(47), P. 19746 - 19749
Published: Jan. 1, 2024
A
gentle
and
remarkably
effective
copper-catalyzed
method
for
the
cascade
sulfonylation
of
alkynes
using
sulfonyl
chlordies
as
direct
sulfonylating
reagents,
is
presented.
Language: Английский