Water-Controlled Geminal Hydroxyphosphinoylation and Diphosphinoylation of Enaminones with H-Phosphine Oxides
The Journal of Organic Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 6, 2025
A
water-controlled
geminal
phosphinoylation
of
enaminones
with
H-phosphine
oxides
has
been
established
through
AlCl3-mediated
C-N
bond
cleavage
in
this
work,
which
provides
a
novel
strategy
for
accessing
various
hydroxy
and
diphosphinoyl
products
3a
4a
high
yields.
The
transformation
features
excellent
functional
group
tolerance,
operational
simplicity,
atom
economy,
is
amenable
complex
molecule
skeletons.
Preliminary
mechanism
studies
suggest
the
conversion
from
to
involve
elimination
hydroxyl
group,
water
temperature
plays
critical
role
influencing
reaction
pathway
product
selectivity.
This
research
significant
value
functionalization
enaminones.
Язык: Английский
Synthesis of 2‐(β‐Trifluoromethyl‐β‐arylethylthio)pyridine through DBU‐Mediated Regioselective Addition of Pyridine‐2(1H)‐thione Onto α‐(Trifluoromethyl)styrenes
Asian Journal of Organic Chemistry,
Год журнала:
2024,
Номер
13(3)
Опубликована: Янв. 8, 2024
Abstract
An
efficient
and
practical
method
for
the
synthesis
of
(β‐trifluoromethyl‐β‐aryl)ethyl
2‐pyridyl
thioethers
via
hydrothiolation
α‐(trifluoromethyl)styrenes
with
pyridine‐2(1
H
)‐thione
was
reported.
The
reaction
proceeded
smoothly
regioselectively
in
an
anti‐Markovnikov
manner
assistance
DBU
afforded
a
variety
trifluoromethyl‐containing
moderate
to
good
yields.
Язык: Английский
Two-step synthesis of vicinal trifluoromethyl primary amines from α-(trifluoromethyl)styrenes and phthalimide
Organic & Biomolecular Chemistry,
Год журнала:
2024,
Номер
22(23), С. 4641 - 4646
Опубликована: Янв. 1, 2024
A
novel
two-step
synthesis
of
β-trifluoromethyl
primary
amines
from
readily
available
α-(trifluoromethyl)styrenes
and
phthalimide
is
developed.
The
first
step
involves
a
hydroamination
between
(PhthNH)
with
the
assistance
base.
Next,
hydrazinolysis
resulting
Язык: Английский
Visible-light-induced hydroxycarboxylation of α-trifluoromethylstyrenes to construct densely functionalized α-CF3 tertiary alcohols
Green Chemistry,
Год журнала:
2024,
Номер
26(15), С. 8694 - 8700
Опубликована: Янв. 1, 2024
Visible-light-induced
hydroxycarboxylation
of
α-trifluoromethylstyrenes
under
an
air
atmosphere
was
developed
to
construct
densely
functionalized
α-CF
3
tertiary
alcohols.
Язык: Английский
Photoinduced Transition‐Metal‐Free Chemodivergent Phosphorylation‐Peroxidation and Oxyphosphorylation of Alkenes
Advanced Synthesis & Catalysis,
Год журнала:
2024,
Номер
unknown
Опубликована: Авг. 22, 2024
Abstract
A
visible‐light‐promoted
chemodivergent
phosphorylation‐peroxidation
and
oxyphosphorylation
of
alkenes
with
phosphine
oxides
HOO
t
Bu
was
realized
under
transition‐metal‐free
conditions.
Using
the
commercially
available
Eosin
Y
as
a
SET‐photocatalyst,
β
‐peroxy‐phosphine
were
selectively
obtained
catalytic
amount
base,
while
addition
acid
led
to
exclusive
formation
‐keto‐phosphine
control
experiments
showed
that
could
also
act
HAT‐catalyst
induce
O−O
bond
cleavage
peroxides
acidic
Язык: Английский
Crystal structure of 1-(4-bromophenyl)-3-(diphenylphosphoryl)-3-hydroxypropan-1-one, C21H18BrO3P
Zeitschrift für Kristallographie - New Crystal Structures,
Год журнала:
2024,
Номер
239(4), С. 731 - 733
Опубликована: Май 31, 2024
Abstract
C
21
H
18
BrO
3
P,
monoclinic,
P
2
1
/
c
(no.
14),
a
=
20.2890(9)
Å,
b
5.9736(2)
16.1577(8)
β
105.371(2)°,
V
1888.24(14)
Å
,
Z
4,
R
gt
(
F
)
0.1359,
w
ref
0.1414,
T
298.00
K.
Язык: Английский
Tunable base-controlled chemoselective synthesis of trifluoromethyl-containing N-substituted benzimidazole-2-thiones and monofluorinated 4H-benzo[4,5]imidazo[2,1-b][1,3]thiazine
Organic & Biomolecular Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 26, 2024
A
base-controlled
synthesis
of
N
-β-CF
3
-substituted
2
H
-benzo[
d
]imidazole-2-thiones
and
2-fluoro-4
-benzo[4,5]imidazo[2,1-
b
][1,3]thiazines
via
hydroamination
or
defluorinative
cyclizations
α-CF
-styrenes
with
2-mercaptobenzimidazole
was
developed.
Язык: Английский