First synthesis of (difluoroiodomethyl)thiophenes through double iodation of 2-(difluoromethylene)but-3-yn-1-yl benzyl sulfides
Daiki Komatsu,
No information about this author
Takeshi Hanamoto
No information about this author
Organic & Biomolecular Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Double
iodation
of
enyne
sulfides
in
a
mixed
solvent
(CHCl
3
/EtOH
=
50/1)
provided
promising
4-(difluoroiodomethyl)-3-iodo-2-substituted
thiophenes
good
to
excellent
yields.
Language: Английский
Recent Advances in Transition-Metal Catalyzed C—H Bond Activation for the Synthesis of C(sp3)-Fluoroalkyl Compounds
Chinese Journal of Organic Chemistry,
Journal Year:
2025,
Volume and Issue:
45(2), P. 516 - 516
Published: Jan. 1, 2025
Language: Английский
Cu(II)/Photoredox-Catalyzed Aminoacylation of Vinyl Bromides
Organic Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 24, 2025
A
novel
C–C
coupling
reaction
of
vinyl
bromides
with
carboxamides
has
been
developed
through
Cu(OAc)2/photocatalysis.
This
process
features
regioselective
carboxamido
carbon-vinylation
under
mild
conditions.
Mechanistic
studies
suggest
that
the
formation
an
acyl-Cu(I)
intermediate
plays
a
crucial
role
regard
to
enabling
this
transformation.
Language: Английский
Photoinduced Metal‐Free Decarboxylative Fluoroalkylation of Alkenes for the Synthesis of N‐Arylbutanamides and Oxindoles
Yi‐Gang Ji,
No information about this author
Z. Li,
No information about this author
Yuqing Yang
No information about this author
et al.
Chemistry - A European Journal,
Journal Year:
2024,
Volume and Issue:
30(68)
Published: Aug. 28, 2024
The
visible
light-induced
decarboxylative
cascade
reaction
of
fluoroalkyl
carboxylic
acids
has
been
achieved
for
the
efficient
synthesis
fluorinated
compounds.
However,
most
transformations
rely
on
noble
iridium
metal
complex.
Herein,
a
metal-free
realized.
This
protocol
features
simple
operation,
transition
free,
and
good
functional
group
tolerance.
Language: Английский
Synthesis of Axially Chiral Monofluoroalkenes via Nickel-Catalyzed Reductive Cross-Coupling of gem-Difluoroalkenes
Organic Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 13, 2024
Enantioenriched
monofluoroalkenes
are
important
structural
motifs
in
life
science
and
functional
materials.
To
date,
only
limited
strategies
were
reported
for
the
synthesis
of
with
stereogenic
carbon
centers;
axially
chiral
counterpart
is
still
highly
desirable.
Herein,
we
report
Ni-catalyzed
defluorinative
cross-electrophile
coupling
Language: Английский