C–H activation-initiated spiroannulation reactions and their applications in the synthesis of spirocyclic compounds
Qianting Zhou,
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Bin Li,
No information about this author
Xinying Zhang
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et al.
Organic & Biomolecular Chemistry,
Journal Year:
2024,
Volume and Issue:
22(12), P. 2324 - 2338
Published: Jan. 1, 2024
This
review
summarizes
the
most
recent
progress
made
in
C–H
bond
activation-initiated
spiroannulation
reactions
and
their
applications
construction
of
structurally
diverse
biologically
valuable
spirocyclic
scaffolds.
Language: Английский
Catalytic System-Controlled [4 + 1] and [4 + 2] Annulation for the Construction of Pyrazolo[1,2-a]indazoles and Pyrazolo[1,2-a]cinnolines from Pyrazolidinones and Diazo Indandiones
Qiang Xiao,
No information about this author
Shulei Hu,
No information about this author
Feifei Fang
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et al.
The Journal of Organic Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 13, 2025
Pyrazolo[1,2-a]indazoles
and
pyrazolo[1,2-a]cinnolines
can
be
constructed
selectively
via
catalytic
system-controlled
C(sp2)-H
activation/[4
+
1]
cyclization
2]
reaction,
utilizing
pyrazolidinones
diazo
indandiones.
Employing
two
different
Rh(III)
catalysts,
we
successfully
synthesized
distinct
types
of
nitrogen-containing
heterocyclic
compounds,
pyrazolo[1,2-a]indazoles
pyrazolo[1,2-a]cinnolines,
respectively.
Moreover,
an
inexpensive
Ru(II)
catalyst
could
also
effectively
generate
with
moderate
to
good
yields.
Overall,
these
methodologies
offer
advantages
such
as
regioselectivity,
broad
substrate
scope,
operational
simplicity,
product
availability.
Language: Английский