Efficient and Regioselective Synthesis of Ortho-Diiodinated Homobenzylic Alcohol Derivatives: In-Silico Evaluation as Potential Anticancer IDO/TDO Inhibitors
Organic & Biomolecular Chemistry,
Journal Year:
2024,
Volume and Issue:
22(36), P. 7395 - 7410
Published: Jan. 1, 2024
A
direct
and
highly
regioselective
method
for
synthesizing
2,6-diiodophenylethanol
is
presented.
In
silico
analysis
shows
compounds
7a,
7p,
7t,
7z
interact
favourably
with
IDO/TDO
receptors,
highlighting
their
unmatched
anticancer
potential.
Language: Английский
Manganese-Catalyzed Cycloalkene Ring Expansion Synthesis of Azaheterocycles
Zhixin Wang,
No information about this author
Hanxiao Xu,
No information about this author
Xuanzhen Han
No information about this author
et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 2, 2024
Herein,
a
Mn
catalytic
protocol
has
been
developed
for
the
cycloalkene
ring
expansion
synthesis
of
azaheterocycles,
allowing
broad-substrate-scope
access
to
pyridine
and
isoquinoline
derivatives.
The
initial
monoaddition
an
azidyl
radical
alkene
further
as-generated
C-radical
addition
O
Language: Английский
Silver-Catalyzed Markovnikov Addition Hydrofunctionalization of Terminal Alkynes: Synthesis of N-Enoxyimides and Oximes
Hafiz Noor,
No information about this author
Shuwei Zhang,
No information about this author
Xiaodong Jia
No information about this author
et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 16, 2024
N-Enoxyimides
are
versatile
and
valuable
synthetic
synthons
in
modern
organic
synthesis
catalysis.
Herein,
a
silver-catalyzed
hydrooxyimidation
of
terminal
alkynes
that
enables
the
N-enoxyimides,
has
been
demonstrated.
The
protocol
features
simple,
step-
atom-efficient,
scalable,
exhibit
broad
scope
functional
group
tolerance
under
mild
conditions.
A
novel
hydrolysis
N-enoxyimides
unexpectedly
provides
corresponding
aromatic
oximes
96%
yield,
showing
potential
application
this
strategy.
Language: Английский