Chromenes
and
their
derivatives
are
abundant
in
natural
products
biologically
active
molecules.
Here
we
summarize
the
decades-long
development
of
transition
metal-catalyzed
site-selective
C–H
functionalization
chromene
derivatives.
This
chapter
describes
2
H
-chromenes,
-chromen-2-ones
(coumarins),
4
-chromenes
-chromen-4-ones
(chromones).
New Journal of Chemistry,
Год журнала:
2024,
Номер
48(47), С. 19742 - 19745
Опубликована: Янв. 1, 2024
Regio-selective
C–H
alkenylation
reaction
with
acrylates
by
a
rhodium-catalyzed
of
PMS
(phenylmethyl
sulfoximine)
directed
2-oxo-2
H
-chromene-3-carboxylic
acid
derivatives.
Advanced Synthesis & Catalysis,
Год журнала:
2020,
Номер
363(4), С. 1088 - 1095
Опубликована: Ноя. 26, 2020
Abstract
Dihydro‐1,4‐thiazine
skeletons
bearing
olefin
fragment
at
their
α‐position
were
prepared
through
a
Pd(OAc)
2
‐catalysed
Fujiwara‐Moritani
type
reaction
via
C−H
alkenylation
with
olefins.
This
approach
is
selective,
generalizable
to
wide
range
of
olefins
and
requires
only
1
eq.
Ag
CO
3
without
the
need
co‐oxidant.
The
bond
activation
proved
be
strongly
dependent
on
olefin's
substitution
while
unfused
dihydro‐1,4‐thiazines
seemed
affected
by
oxidation
state
sulfur
atom.
utility
obtained
was
demonstrated
implication
in
dipolar
cycloaddition
non‐stabilized
azomethine
ylide.
magnified
image
Organic & Biomolecular Chemistry,
Год журнала:
2021,
Номер
19(34), С. 7470 - 7474
Опубликована: Янв. 1, 2021
A
simple
method
for
the
synthesis
of
trisubstituted
furans
has
been
disclosed
using
an
Rh(
iii
)-catalyst
by
C
vinyl
–H
bond
activation,
with
silver
salt
Ag(
i
)
is
playing
a
dual
role
–
halide
scavenger
and
Lewis
acid
catalyst
promoting
Paal–Knorr
type
cyclization.
Chromenes
and
their
derivatives
are
abundant
in
natural
products
biologically
active
molecules.
Here
we
summarize
the
decades-long
development
of
transition
metal-catalyzed
site-selective
C–H
functionalization
chromene
derivatives.
This
chapter
describes
2
H
-chromenes,
-chromen-2-ones
(coumarins),
4
-chromenes
-chromen-4-ones
(chromones).