Photocatalytic Enantioselective Radical Cascade Multicomponent Minisci Reaction of β‐Carbolines Using Diazo Compounds as Radical Precursors
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(25)
Published: April 19, 2024
Abstract
Here,
a
photocatalytic
asymmetric
multicomponent
cascade
Minisci
reaction
of
β‐carbolines
with
enamides
and
diazo
compounds
is
reported,
enabling
an
effective
enantioselective
radical
C─H
functionalization
high
yields
enantioselectivity
(up
to
83%
yield
95%
ee).
This
protocol
exhibits
step
economy,
chemo‐/enantio‐selective
control,
good
functional
group
tolerance,
allowing
access
variety
valuable
chiral
β‐carbolines.
Notably,
are
suitable
precursors
in
reactions.
Moreover,
the
efficiency
practicality
this
approach
demonstrated
by
synthesis
bioactive
natural
products.
Language: Английский
Photocatalytic Synthesis of Isoquinolinediones via the Cascade Reaction of N-Alkyl-N-methylacrylamides with Diazo Compounds
Chenyue Zhao,
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Heran Yang,
No information about this author
Kai Xu
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et al.
Organic Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 25, 2025
Carbon
radicals
generated
from
acceptor
diazo
compounds
prefer
to
add
electron-rich
olefins
and
heteroarenes
due
their
containing
electron-withdrawing
groups.
Herein,
a
cascade
reaction
of
with
electron-deficient
is
developed.
In
the
presence
visible
light
Ru
catalyst,
generate
carbon
via
proton-coupled
electron
transfer
process,
followed
by
addition
various
N-alkyl-N-methylacrylamides
subsequent
cyclization
give
series
acyl-substituted
isoquinolinediones.
Language: Английский
Iron-Catalyzed C–H Arylphosphorylation of Quinoxalines
Maoyi Dai,
No information about this author
Meilan Xu,
No information about this author
Xiaoting Gu
No information about this author
et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(36), P. 7672 - 7677
Published: Sept. 4, 2024
A
one-pot
strategy
for
iron-catalyzed
C2,3-H
arylphosphorylation
of
electron-deficient
quinoxalines
with
phosphines
and
aryl
compounds
is
reported.
The
proposed
method
features
the
use
non-noble
metal
catalysts,
capacity
utilizing
multiple
as
substrates,
simultaneous
formation
C-P
C-C
bonds
in
one
pot,
simplicity
its
operation,
mildness
reaction
conditions,
compatibility
a
wide
range
substrates.
Moreover,
it
offers
practical
route
direct
access
to
2-aryl-3-phosphino
Language: Английский