Heterocycles,
Год журнала:
2020,
Номер
100(5), С. 719 - 719
Опубликована: Янв. 1, 2020
An
efficient
method
for
the
synthesis
of
multi-substituted
pyrroles
was
developed
using
basic
cyclization
readily
accessible
N-Boc-N-propargylenamines.
Despite
conditions,
cleavage
N-Boc
group
occurred
easily.The
process
rapid
and
afforded
N-H-pyrroles
with
wide
functional
tolerance
in
high
yields.
The Journal of Organic Chemistry,
Год журнала:
2020,
Номер
86(1), С. 110 - 127
Опубликована: Дек. 2, 2020
A
three-component
reaction
has
been
developed
for
the
construction
of
multiaryl-substituted
pyrrole
derivatives
from
arylketones,
amines,
and
nitrovinylarenes
under
metal-free
conditions.
Hence,
homologous
1,2,4-triaryl-substituted
products
were
obtained
in
good
to
high
yields.
Furthermore,
2,3,5-triaryl-substituted
pyrroles
selectively
formed
absence
nitrovinylarenes.
The
photophysical
properties
some
have
investigated
show
aggregation-induced
emission
(AIE)
activity.
Organic & Biomolecular Chemistry,
Год журнала:
2023,
Номер
21(25), С. 5265 - 5273
Опубликована: Янв. 1, 2023
Diastereoselective
formation
of
pyrrolidene-2-ylidenes
by
the
Huisgen
reaction
hydrogen-bond-assisted
azomethine
ylides
with
β-bromo-β-nitrostyrenes
is
reported.
Chemistry & Biodiversity,
Год журнала:
2023,
Номер
21(1)
Опубликована: Ноя. 28, 2023
Abstract
Multi‐Drug
Resistance
(MDR)
is
one
of
the
most
frequent
problems
observed
in
course
cancer
chemotherapy.
Cells
under
treatment,
tend
to
develop
survival
mechanisms
drug‐action
thus
generating
drug‐resistance.
One
important
mechanism
get
it
over
expression
P‐gp
glycoprotein,
which
acts
as
an
efflux‐pump
releasing
drug
outside
cell.
A
strategy
for
a
succesfull
treatment
consists
co‐administration
compound
that
against
and
another
cell
during
Ningalins
are
pyrrole‐containing
naturally
occurring
compounds
isolated
mainly
from
marine
tunicate
Didemnum
spp
also
they
some
top
reversing
agents
MDR
acting
on
P‐gp.
Considering
relevance
displayed
these
alkaloids
or
their
core
therapy,
all
total
synthesis
described
date
members
ningalins
family
reviewed
herein.
RSC Advances,
Год журнала:
2024,
Номер
14(21), С. 14835 - 14846
Опубликована: Янв. 1, 2024
In
this
work,
we
have
described
the
use
of
α-bromonitrostyrenes
in
synthesis
a
wide
variety
carbocyclic
and
heterocyclic
compounds
under
organocatalysis,
metal
catalysis,
base-catalysis
systems
as
well
catalyst-free
reactions.
Chinese Journal of Organic Chemistry,
Год журнала:
2023,
Номер
43(12), С. 4168 - 4168
Опубликована: Янв. 1, 2023
β-Nitrostyrene
has
a
variety
of
biological
activities
and
is
also
an
important
intermediate
in
organic
synthesis,
which
can
participate
chemical
reactions
due
to
its
active
properties,
attracted
extensive
attention
from
researchers.The
involving
nitrostyrene
compounds
recent
years
are
summarized,
the
reaction
divided
into
denitrification
carbon-carbon
double
bonds
according
sites,
expecting
provide
reference
for
new
with
β-nitrostyrene
as
substrates.Keywords
β-nitrostyrene;
denitrogenation
reaction;
carbon
bond
β-硝基苯乙烯是重要的有机化合物,
广泛存在于具
有多种生物活性的化合物结构和药物分子中,
其本身也
具有抑制人端粒酶
[1]
、杀菌
[2][3]
及抗肿瘤
[4][5]
等活性.近年
来,
其在有机合成方向的应用也越来越被重视.β-硝基苯乙烯类化合物因兼具硝基和碳碳双键而
拥有较为活泼的性质,
可参与多种类型的反应.根据文
献调研,
目前尚无相关专题综述对
β-硝基苯乙烯类化合
物参与的反应进行归纳总结.最近几年该类化合物的应
用策略越来越多,
因此,
很有必要对其进行梳理,
以期
为从事有机合成及相关领域的研究者提供有益的借鉴
和参考.以
β-硝基苯乙烯类化合物为底物的反应主要可
以分为脱硝基反应和碳碳双键参与的反应.本文将从以
上两种反应方式对近年来的重要相关文献进行综述,
并
简要介绍其反应特点和反应机理.
脱硝基反应β-硝基苯乙烯类化合物分子结构中,
由于存在强吸
电子基团硝基,
使与之相连的双键
π
电子云发生极化,
不仅能够脱硝基构建各种环状骨架
[6][7][8]
,
亦可转化成新
的官能团
[9][10]
生成不同的化合物.1.1
脱硝成环
1.1.1脱硝基形成
C
环化合物
以
β-硝基苯乙烯为原料能够合成各种碳环化合物.2016
年,
Swamy
课题组
[11]
报道了
Pd(OAc)
2
催化的内炔
烃与硝基苯乙烯制备
2,3-二取代茚酮的反应.环化反应
通过催化剂与硝基苯乙烯的金属转移和炔烃的插入进
行,
硝基苯乙烯基团的高亲电性为
C-H
和
C-C
裂解
环化提供了条件.该反应以中等至良好的产率和高区域
选择性进行(Eq.1).
Convenient
access
to
6-alkylsulfonylmethyl
phenanthridines
has
been
demonstrated
both
under
thermal
and
visible-light
photoredox-catalyzed
conditions.
A
cascade
of
radical
cyclization
is
triggered
on
exposure
biphenyl
vinyl
azides
the
in-situ
generated
alkyl
sulfonyl
radicals
from
4-substituted
Hanztsch
esters
in
presence
an
SO2
surrogate.
Transition
metal-free,
mild
reaction
conditions,
broad
substrate
scope
constitute
some
highlights
approach.
Also,
synthetic
utility
accessed
demonstrated.