N,N-Dimethylformamide’s Participation in Domino Reactions for the Synthesis of Se-Phenyl Dimethylcarbamoselenoate Derivatives
Ruren Xu,
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Shanshan Hu,
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L. Eduardo Wu
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et al.
Molecules,
Journal Year:
2025,
Volume and Issue:
30(3), P. 747 - 747
Published: Feb. 6, 2025
N,N-dimethylformamide’s
(DMF)
participation
in
domino
reactions
has
been
developed.
Starting
from
substituted
halogenobenzenes
and
selenium
powder,
versatile
biologically
active
Se-phenyl
dimethylcarbamoselenoate
derivatives
were
efficiently
synthesized
under
mild
reaction
conditions.
The
mechanism
was
studied
using
control
experiments.
These
protocols
involve
a
wider
substrate
scope
provide
an
economical
approach
toward
C–selenium
bond
formation.
Language: Английский
Heteroarylation of Organophosphonium Salts with Indoles in Water: Synthesis of Symmetrical and Unsymmetrical 3,3'‐Bisindolylmethane Derivatives
Xin-Long Luo,
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Wen-Jun Ji,
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Zi-Lun Yu
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et al.
European Journal of Organic Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 16, 2024
Abstract
A
method
for
the
synthesis
of
symmetrical
and
unsymmetrical
3,3′‐bis(indolyl)methanes
(3,3′‐BIMs)
has
been
developed
through
direct
heteroarylation
indolyl‐containing
di(hetero)aryl
phosphonium
salts
with
indole
derivatives
in
aqueous
media.
This
metal‐free
reaction
proceeds
smoothly
under
mild
conditions,
eliminating
need
hazardous
solvents
expensive
additives/catalysts
typically
used
conventional
routes,
thereby
highlighting
synthetic
practicality
efficiency
process.
The
success
this
approach
is
largely
attributed
to
role
water
as
a
promoter,
facilitating
C−P
bond
functionalization
salts.
Furthermore,
demonstrates
broad
substrate
scope,
good
functional
group
tolerance,
excellent
scalability.
Moreover,
protocol
can
also
be
extended
triindolylmethane
compound
diarylmethylated
indole.
Language: Английский