Visible-Light-Mediated Deaminative Alkylation of Primary Amines with Silacarboxylic Acids via Isonitrile Formation
Carla Pérez-Sánchez,
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Thomas Rigotti,
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Mariola Tortosa
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et al.
Organic Letters,
Journal Year:
2025,
Volume and Issue:
27(2), P. 583 - 587
Published: Jan. 7, 2025
The
functionalization
of
the
C–N
bond
amines
is
a
straightforward
strategy
for
construction
complex
scaffolds
or
late-stage
pharmaceuticals.
Herein,
we
describe
photoredox-catalyzed
deaminative
alkylation
primary
amine-derived
isonitriles
that
provides
unnatural
amino
acid
derivatives
under
mild
conditions.
use
silacarboxylic
acids
as
silyl
radical
precursors
enables
generation
carbon-centered
radicals
allow
Csp3–Csp3
bonds
via
Giese-type
addition,
avoiding
undesired
hydrodeamination
product.
Language: Английский
Photocatalytic Denitrative Alkenylation of Nitroalkanes
Ayumi Osawa,
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K Uemura,
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Shuji Murakami
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et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 25, 2024
Reductive
radical
generation
has
become
a
cornerstone
of
modern
photoredox
chemistry.
However,
the
synthesis
functionalized
precursors
remains
tedious
multistep
process.
In
this
study,
we
focus
on
potential
nitro
group
as
redox-active
functional
and
present
denitrative
alkenylation
nitroalkanes,
facilitated
by
photoreductive
alkyl
radicals
from
nitroalkanes.
By
taking
advantage
facile
α-functionalization
successfully
generate
various
radicals,
which
are
subsequently
used
in
reactions.
Language: Английский