Organic Letters,
Год журнала:
2023,
Номер
25(51), С. 9142 - 9146
Опубликована: Дек. 19, 2023
This
paper
describes
a
B(C6F5)3-catalyzed
hydrogenation
of
β-substituted
α,β-unsaturated
imines
by
using
as
low
0.2
mol
%
catalyst.
A
variety
tetrasubstituted
enamines
were
afforded
in
95-99%
yields.
It
provides
an
efficient
and
facile
way
without
the
need
for
column
chromatography
purification.
Chemical Reviews,
Год журнала:
2022,
Номер
122(18), С. 14346 - 14404
Опубликована: Авг. 16, 2022
Asymmetric
catalysis
has
emerged
as
a
general
and
powerful
approach
for
constructing
chiral
compounds
in
an
enantioselective
manner.
Hence,
developing
novel
ligands
catalysts
that
can
effectively
induce
asymmetry
reactions
is
crucial
modern
chemical
synthesis.
Among
such
catalysts,
dienes
their
metal
complexes
have
received
increased
attention,
great
progress
been
made
over
the
past
two
decades.
This
review
provides
comprehensive
critical
information
on
essential
aspects
of
diene
importance
asymmetric
catalysis.
The
literature
covered
ranges
from
August
2003
(when
first
effective
ligand
was
reported)
to
October
2021.
divided
into
parts.
In
part,
are
categorized
according
structures,
preparation
methods
summarized.
second
applications
transformations
presented
reaction
types.
Chemical Society Reviews,
Год журнала:
2023,
Номер
52(24), С. 8580 - 8598
Опубликована: Янв. 1, 2023
This
review
provides
an
overview
of
the
important
progress
in
FLP-catalyzed
asymmetric
reactions
made
over
past
15
years,
and
both
merits
limitations
FLP-catalysis
have
been
highlighted.
The Journal of Organic Chemistry,
Год журнала:
2023,
Номер
88(5), С. 3335 - 3339
Опубликована: Фев. 17, 2023
A
chiral
phosphoric
acid
catalyzed
asymmetric
transfer
hydrogenation
of
quinolines
with
regenerable
dihydrophenanthridine
derived
by
a
borane-catalyzed
phenanthridine
under
H2
has
been
successfully
realized.
Despite
the
competition
racemic
pathway,
variety
tetrahydroquinolines
were
furnished
in
high
yields
up
to
91%
ee.
This
paper
describes
an
asymmetric
hydrogenation
of
1,3-disubstituted
isoquinolines
catalyzed
by
chiral
borane
derived
from
alkene,
giving
the
desired
cis-products
in
high
yields
with
up
to
96%
ee.
In
particular,
challenging
1,3,4-trisubstituted
could
proceed
smoothly
afford
corresponding
products
moderate
ee's
for
first
time.
The Journal of Organic Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 8, 2025
An
enantioselective
synthesis
of
2-aryl
3,3-disubstituted
3H-indoles
has
been
successfully
developed
via
a
deracemization
process
involving
borane-catalyzed
hydrogenation
and
chiral
phosphoric-acid-catalyzed
asymmetric
transfer
hydrogenation.
A
variety
were
effective
substrates
to
afford
the
desired
indolines
in
86-95%
yields
with
45-92%
ee's.
The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
89(5), С. 3666 - 3671
Опубликована: Фев. 15, 2024
The
asymmetric
hydrogenation
of
quinoxalines
represents
one
the
most
efficient
approaches
for
synthesis
optically
active
tetrahyroquinoxalines.
In
this
paper,
we
demonstrate
a
metal-free
transfer
2-substituted
with
regenerable
dihydrophenanthridine
under
H2
using
combination
chiral
phosphoric
acid
and
achiral
borane
as
catalysts.
A
wide
range
tetrahydroquinoxalines
were
produced
in
high
yields
≤98%
ee.
Angewandte Chemie International Edition,
Год журнала:
2023,
Номер
63(5)
Опубликована: Дек. 9, 2023
The
asymmetric
reduction
of
1,2-diketones
for
the
synthesis
optically
active
1,2-diols,
especially
1,2-anti-diols,
remains
a
formidable
challenge.
In
this
paper,
we
describe
first
highly
stereoselective
hydrosilylation
unsymmetrical
vicinal
diketones
with
PhSiH
Chinese Journal of Chemistry,
Год журнала:
2023,
Номер
42(6), С. 631 - 635
Опубликована: Ноя. 21, 2023
Comprehensive
Summary
The
asymmetric
hydrogenation
of
N
‐heteroarenes
provides
an
efficient
method
for
the
synthesis
optically
active
cyclic
secondary
amines.
In
this
paper,
we
described
phenanthridines
using
a
chiral
mono‐alkene‐derived
borane.
A
variety
dihydrophenanthridines
were
furnished
in
high
yields
with
up
to
93%
ee.
current
catalytic
system
was
very
sensitive
steric
hindrance
phenanthridines.
Bulky
substituents
at
one
phenyl
group
required
obtain
enantioselectivity.
But
large
on
carbon
C=N
bonds
would
diminish
reactivity
sharply.
Chinese Journal of Organic Chemistry,
Год журнала:
2023,
Номер
43(10), С. 3558 - 3558
Опубликована: Янв. 1, 2023
Organosilicon
products
have
become
an
indispensable
part
of
our
lives
today.Catalytic
hydrosilylation
reaction
is
one
the
important
methods
for
preparing
organosilicon
chemicals
and
materials.The
research
development
inexpensive
excellent
catalysts
received
extensive
attention.At
present,
on
catalytic
mainly
focuses
exploring
properties
new
noble
metal
non-precious
complexes.However,
due
to
high
cost
metals
low
activity
non-noble
complexes,
photocatalysis
environmentally
friendly
safe
method.Catalytic
photocatalytic
reactions
much
attention.In
this
paper,
progress
in
recent
years
introduced.