Radical hydroboration for the synthesis of organoboron compounds
Chemical Communications,
Journal Year:
2024,
Volume and Issue:
60(32), P. 4275 - 4289
Published: Jan. 1, 2024
This
review
describes
the
recent
research
on
radical
hydroboration,
which
covers
different
boron
sources
including
N-heterocyclic
carbene
borane,
bis(pinacolato)diboron
and
pinacolborane,
as
well
strategies
in
boryl
generation.
Language: Английский
Visible‐Light‐Driven Germyl Radical Generation via EDA‐Catalyzed ET–HAT Process
Kaito Yoshizawa,
No information about this author
Bi‐Xiao Li,
No information about this author
Taro Matsuyama
No information about this author
et al.
Chemistry - A European Journal,
Journal Year:
2024,
Volume and Issue:
30(41)
Published: May 8, 2024
Abstract
We
have
established
a
facile
and
efficient
protocol
for
the
generation
of
germyl
radicals
by
employing
photo‐excited
electron
transfer
(ET)
in
an
donor‐acceptor
(EDA)
complex
to
drive
hydrogen‐atom
(HAT)
from
hydride
(R
3
GeH).
Using
catalytic
amount
EDA
commercially
available
thiol
benzophenone
derivatives,
ET‐HAT
cycle
smoothly
proceeds
simply
upon
blue‐light
irradiation
without
any
transition
metal
or
photocatalyst.
This
also
affords
silyl
radical
hydride.
Language: Английский
Photoinduced Dearomative Multiple Functionalization of Quinolines to Construct Highly Substituted 3D Frameworks
Yuki Nagashima,
No information about this author
Asuha Shimose
No information about this author
Synlett,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 18, 2025
Abstract
Dearomative
functionalization
of
quinolines
expands
the
chemical
diversity
highly
functionalized
3D
frameworks,
such
as
1,2,3,4-
and
5,6,7,8-tetrahydroquinoline
derivatives,
which
are
important
pharmacophores,
with
minimal
synthetic
costs.
In
this
short
review,
we
cover
recent
reports
on
visible-light-induced
dearomative
an
emphasis
reaction
design/strategies
mechanistic
studies
provide
a
theoretical
basis
for
developing
further
syntheses
in
future.
1
Introduction
2
Functionalizations
through
Formation
Photoexcited
Quinolines
3
Reagents/Intermediates
4
Conclusion
Language: Английский