Rh(III)-Catalyzed Successive C–H Activations of 2-Phenyl-3H-indoles and Cyclization Cascades to Construct Highly Fused Indole Heteropolycycles
Ju Gao,
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Keyu Luo,
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Xiaohui Wei
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et al.
Organic Letters,
Journal Year:
2023,
Volume and Issue:
25(19), P. 3341 - 3346
Published: May 5, 2023
Rh(III)-catalyzed
successive
C-H
activations
of
2-phenyl-3H-indoles
and
cyclization
cascades
with
diazo
compounds
were
developed
to
construct
highly
fused
indole
heteropolycycles
a
broad
range
substrates
good
yields.
In
particular,
this
transformation
included
two
unusual
[3+3]
[4+2]
sequential
cascades,
in
which
the
compound
played
different
role
processes,
while
simultaneously
forming
polycyclic
scaffold
new
quaternary
carbon
center.
Language: Английский
Modular Assembly of Pyrrolo[3,4-c]isoquinolines through Rh-Catalyzed Cascade C–H Activation/Annulation of O-Methyl Aryloximes with Maleimides
Yinsong Wu,
No information about this author
Yanan Liu,
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Yangzilin Kong
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et al.
The Journal of Organic Chemistry,
Journal Year:
2024,
Volume and Issue:
89(12), P. 8447 - 8457
Published: June 4, 2024
An
efficient
and
practical
strategy
for
the
construction
of
pyrrolo[3,4-
Language: Английский
Mechanistic insights to define the directional role of hydrogen-bonding network between aryl oximes and propargyl alcohols in Rh(III) catalysis
Yi Wang,
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Ping Qi,
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Hui Gao
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et al.
Molecular Catalysis,
Journal Year:
2023,
Volume and Issue:
550, P. 113448 - 113448
Published: Sept. 15, 2023
Language: Английский
Rh(II)-Catalyzed Selective C(sp3)–H/C(sp2)–H Bonds Cascade Insertion to Construct [6–8–6] Benzo-Fused Scaffold
T.X. Yu,
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Feifei Fang,
No information about this author
Haowen Shou
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et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 10, 2024
The
fused
eight-membered
carbocycles
(EMCs)
play
vital
roles
in
the
medicinal
and
biological
investigations
of
many
natural
products
marketed
drugs.
traditional
synthesis
[6-8-6]
benzo-fused
derivatives
involves
multistep
reactions
low
yields,
making
development
a
one-step
method
more
challenging
work.
Here,
we
present
novel
strategy
for
construction
scaffold
from
propargyl
diazoacetates
substituted
with
benzyl-nitrogen
heterocyclic
ring
via
Rh(ll)-catalyzed
carbene/alkyne
metathesis
(CAM)
selective
C-H
bond
insertion.
This
exhibits
specific
substrate
scope,
simple
operation,
mild
reaction
conditions,
high
atom
efficiency.
Mechanistically,
process
sequential
CAM,
1,3-H-shift,
intramolecular
nucleophilic
attack,
C(sp
Language: Английский