Concomitant (3 + 3) Annulation/Fragmentation of Triazinanes with Enamines: Electrosynthesis of Multisubstituted Dihydropyrimidines
Organic Letters,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 6, 2025
An
electro-oxidative
formal
(3
+
3)
annulation
of
1,3,5-triazinanes
with
enamines
toward
multisubstituted
1,2-dihydropyrimidines
is
reported.
This
metal-free
mild
protocol
offers
wide
functional
group
tolerance,
and
heterocycles
an
unexplored
molecular
scaffold
were
constructed
in
excellent
yields.
Mechanistically,
the
electro-oxidation
triazinane
nucleophilic
reactivity
enamine
result
a
concomitant
annulation-fragmentation
process,
leading
to
six-membered
heterocyclic
product.
Язык: Английский
Divergent Sc(OTf)3‐Catalyzed Tandem Cyclization of o‐Hydroxyphenyl Enaminones with 1,3,5‐Triazinanes: Access to C3‐Aminomethyl Chromones and Tetrahydropyrimidines
Asian Journal of Organic Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 9, 2024
Abstract
A
Sc(OTf)
3
‐catalyzed
tandem
cyclization
reaction
of
o
‐hydroxyphenyl
enaminones
with
1,3,5‐triazinanes
has
been
developed
to
generate
two
distinct
annulated
products
in
moderate
good
yields,
which
is
dominated
by
the
electronic
characteristics
1,3,5‐triazinanes.
The
1,3,5‐triaryl‐1,3,5‐triazinane
reacted
as
C−N
synthon
produce
C3‐aminomethyl
chromone,
while
1,3,5‐trialkyl‐1,3,5‐triazinane
acted
C−N−C−N
synthons
deliver
N
,
‐dialkyl
tetrahydropyrimidine
a
free
hydroxyl
group.
Язык: Английский