RSC Advances,
Journal Year:
2023,
Volume and Issue:
13(39), P. 27456 - 27460
Published: Jan. 1, 2023
AB
2
C
type
four
component
quadruple
cascade
reaction
between
MBH
acetate,
1,3-indanedione
and
aldehydes
via
[1
+
1
3]
annulation
progressed
through
Knoevenagel/Michael/Michael/Michael
sequence
for
the
synthesis
of
b
is-spirocyclohexane.
The Journal of Organic Chemistry,
Journal Year:
2021,
Volume and Issue:
86(23), P. 16425 - 16433
Published: Nov. 18, 2021
The
aza-Prins
reaction
of
6,7-dimethoxy-3-vinyl-1,2,3,4-tetrahydroquinoline
(1)
with
1,2-dicarbonyl
compounds
proceeded
smoothly
in
the
presence
HCl,
and
corresponding
tricyclic
benzazocines
were
isolated
yields
20–86%.
a
stereoselective
manner,
formation
2,4-trans
isomer
was
observed.
1
an
enantiopure
ketoester
gave
benzazocine
as
mixture
diastereomers.
diastereomers
easily
separated
converted
to
benzazocines.
synthesis
spirooxindole
derivatives
achieved
by
isatin
derivatives.
RSC Advances,
Journal Year:
2023,
Volume and Issue:
13(39), P. 27456 - 27460
Published: Jan. 1, 2023
AB
2
C
type
four
component
quadruple
cascade
reaction
between
MBH
acetate,
1,3-indanedione
and
aldehydes
via
[1
+
1
3]
annulation
progressed
through
Knoevenagel/Michael/Michael/Michael
sequence
for
the
synthesis
of
b
is-spirocyclohexane.