Syntheses of Unsymmetric (Sulfoxylidene)ureas from NH-Sulfoximines and Dioxazolones Assisted by 2,2,2-Trifluoroethanol
Organic Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 27, 2025
Ureas
and
sulfoximines
are
relevant
as
natural
products
pharmaceuticals.
The
fusion
of
these
two
frameworks
results
in
(sulfoxylidene)ureas.
Herein,
we
present
a
convenient
method
to
access
such
compounds
from
NH-sulfoximines
dioxazolones.
reactions
assisted
by
2,2,2-trifluoroethanol
(TFE),
yielding
the
desired
moderate
good
yields
under
mild
reaction
conditions.
process,
which
involves
Curtius
rearrangement,
is
characterized
its
simplicity
absence
any
additional
activator
rendering
it
appealing
for
applications
medicinal
chemistry.
Language: Английский
Intermolecular amination of Ethyl Benzo ylacetate via photocatalytic nitrene transfer reactions
Yujing Guo,
No information about this author
Yifan Guo,
No information about this author
Luyao Ding
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et al.
Organic Chemistry Frontiers,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
This
study
reports
a
photocatalytic
nitrene
transfer
reaction
of
1,3-dicarbonyl.
A
broad
range
substrates
and
iodinanes
are
shown,
enabling
direct
C–H
functionalization
without
the
need
for
pre-formed
nucleophilic
enolate
equivalents.
Language: Английский
Tertiary Amine‐Catalyzed Stereoretentive Multi‐Component Cascade Reaction of Carboxylic Acids: Facile Synthesis of Cyclic Ureas/Urethanes
Yi Hu,
No information about this author
Yifei Cai,
No information about this author
Yanfei Liu
No information about this author
et al.
Chinese Journal of Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 29, 2025
Comprehensive
Summary
Herein,
we
developed
a
tertiary
amine‐catalyzed
stereoretentive
multi‐component
cascade
reaction
featuring
an
amidation/[4
+
1]
annulation/decarboxylation/Curtius
rearrangement/[2
n
]
annulation
sequence.
This
metal‐free
and
step‐economic
method
provided
broad
range
of
cyclic
ureas/urethanes
in
green
solvent
under
mild
conditions
without
employing
explosive
toxic
reagents.
Importantly,
this
generated
isocyanates
situ
catalytic
via
decarboxylation/Curtius
rearrangement
process
dioxazolones.
Language: Английский
Visible-light-induced Fe(iii)-promoted reduction amidation of 1,4,2-dioxazol-5-one
New Journal of Chemistry,
Journal Year:
2024,
Volume and Issue:
48(30), P. 13654 - 13658
Published: Jan. 1, 2024
This
method
describes
the
iron-promoted
amidation
of
dioxazolone
under
visible
light
to
obtain
aromatic/alkyl
substituted
amides.
Language: Английский