Asian Journal of Organic Chemistry,
Год журнала:
2022,
Номер
12(1)
Опубликована: Дек. 15, 2022
Abstract
An
efficient
synthesis
of
densely
1,2,4‐triazoles
has
been
achieved
by
[3+2]
cycloaddition
nitrileimides
with
amidine
hydrochlorides
under
transition
metal‐free
conditions.
This
method
features
mild
reaction
conditions,
wide
substrate
scope
and
good
functional
group
tolerance.
A
series
aryl,
heterocyclic
alkyl
substituted
3‐CF
3
‐1,2,4‐triazoles
were
synthesized
smoothly
the
promotion
NaHCO
yield
up
to
96%.
In
addition,
both
gram‐scale
synthetic
transformations
are
elaborated
indicate
utility
this
reaction.
Chemistry - An Asian Journal,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 7, 2024
Solvent
plays
an
important
role
in
many
chemical
reactions.
The
C-H
activation
has
been
one
of
the
most
powerful
tools
organic
synthesis.
These
reactions
are
often
assisted
by
solvents
which
not
only
provide
a
medium
for
but
also
facilitate
reaching
to
product
stage.
solvent
helps
reaction
profile
both
chemically
and
energetically
reach
targeted
product.
Organic
transformations
via
from
assistance
perspective
discussed
this
review.
Various
such
as
tetrahydrofuran
(THF),
MeCN,
dichloromethane
(DCM),
dimethoxyethane
(DME),
1,2-dichloroethane
(1,2-DCE),
dimethylformamide
(DMF),
dimethylsulfoxide
(DMSO),
isopropyl
nitrile
(
RSC Mechanochemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Янв. 1, 2024
A
series
of
trifluoromethylated
pyrrolo[3,4-
c
]pyrazoles
were
obtained
via
mechanochemical
(3
+
2)-cycloaddition
in
situ
generated
trifluoroacetonitrile
imines
with
maleimide
and
its
N
-aliphatic/aromatic
analogues.
Asian Journal of Organic Chemistry,
Год журнала:
2022,
Номер
12(1)
Опубликована: Дек. 15, 2022
Abstract
An
efficient
synthesis
of
densely
1,2,4‐triazoles
has
been
achieved
by
[3+2]
cycloaddition
nitrileimides
with
amidine
hydrochlorides
under
transition
metal‐free
conditions.
This
method
features
mild
reaction
conditions,
wide
substrate
scope
and
good
functional
group
tolerance.
A
series
aryl,
heterocyclic
alkyl
substituted
3‐CF
3
‐1,2,4‐triazoles
were
synthesized
smoothly
the
promotion
NaHCO
yield
up
to
96%.
In
addition,
both
gram‐scale
synthetic
transformations
are
elaborated
indicate
utility
this
reaction.