Green Chemistry,
Journal Year:
2021,
Volume and Issue:
23(23), P. 9422 - 9427
Published: Jan. 1, 2021
Electrochemical
N
-cyanation
of
secondary
amines
and
α
C
tertiary
have
been
established
under
transition
metal-free
conditions,
which
provide
cyanamides
nitriles
with
good
functional
group
tolerance
from
simple
systems.
Chinese Journal of Organic Chemistry,
Journal Year:
2021,
Volume and Issue:
41(11), P. 4138 - 4138
Published: Jan. 1, 2021
Organophosphorus
compounds
bearing
C(sp
3
)-P
bonds
have
been
widely
used
in
organic
synthesis,
bioorganic
and
medical
chemistry,
agrochemicals,
flame
retardants
extractants.In
recent
years,
the
direct
phosphorylation
of
C-H
has
received
much
attention
because
this
strategy
represents
more
straightforward,
efficient
atom-economic
construction
C-P
bonds.The
advances
)-H
using
secondary
phosphine
oxides
phosphite
esters
as
phosphorus
sources
since
2009
are
reviewed,
corresponding
reactions
categorized
five
types
according
to
structure
bonds.
RSC Advances,
Journal Year:
2022,
Volume and Issue:
12(47), P. 30466 - 30479
Published: Jan. 1, 2022
The
electrochemical
reaction
of
amines,
nitriles,
amides,
nitroaromatics,
and
imines
has
been
proven
to
be
a
valuable
method
for
the
synthesis
various
nitrogen-containing
organic
compounds.
Synlett,
Journal Year:
2020,
Volume and Issue:
31(12), P. 1191 - 1196
Published: April 17, 2020
Mild
experimental
conditions
for
a
direct
phosphonylation
of
an
easily
cleavable
N-carbamate-tetrahydroisoquinoline
have
been
described
under
constant
current
electrolysis.
The
developed
electrochemical
process
allowed
to
prepare
α-aminophosphonates
in
moderate
good
yields.
On
the
basis
results,
mechanism
proceeding
through
convergent
paired
was
enabled
be
postulated.
Chinese Journal of Organic Chemistry,
Journal Year:
2021,
Volume and Issue:
41(8), P. 3223 - 3223
Published: Jan. 1, 2021
Metal-free
electrochemical
oxidation
cyanation
and
phosphonylation
reactions
had
been
developed,
in
which
2,2,6,6-tetramethylpiperidinyl-N-oxyl
(TEMPO)
reduced
the
electrode
potential
of
substrate
avoided
over
some
electron
rich
aromatic
amines
under
conditions.This
protocol
good
functional
group
compatibility,
made
it
to
be
a
practical
efficient
method
synthesize
α-aminonitriles
α-amino
phosphonates
mild
conditions.Preliminary
study
indicated
that
formation
product
was
through
Shono
imine
species.
Green Chemistry,
Journal Year:
2021,
Volume and Issue:
23(23), P. 9422 - 9427
Published: Jan. 1, 2021
Electrochemical
N
-cyanation
of
secondary
amines
and
α
C
tertiary
have
been
established
under
transition
metal-free
conditions,
which
provide
cyanamides
nitriles
with
good
functional
group
tolerance
from
simple
systems.