Effect of the support alkyl chain nature in the functional properties of the immobilized lipases
Enzyme and Microbial Technology,
Journal Year:
2025,
Volume and Issue:
184, P. 110583 - 110583
Published: Jan. 11, 2025
Language: Английский
Phospha-Michael addition of biphenylphosphine oxide to chalcones and α,β-unsaturated esters using the organocatalyst 1,1-diaminobenzalazine
Tetrahedron Letters,
Journal Year:
2023,
Volume and Issue:
122, P. 154505 - 154505
Published: April 21, 2023
Language: Английский
Synthesis of functionalized 1,4-dihydropyridines containing benzosultams catalyzed by lipase
New Journal of Chemistry,
Journal Year:
2023,
Volume and Issue:
47(20), P. 9708 - 9713
Published: Jan. 1, 2023
As
a
base
structural
unit,
1,4-dihydropyridines
(DHPs)
containing
benzosultams
widely
exist
in
bioactive
molecules
and
drugs.
Language: Английский
A Practical Synthesis of 2‐Arylimino‐2H‐Chromenes via Biocatalytic System in Water
Jinglin Ma,
No information about this author
Fengxi Li,
No information about this author
Yuelin Xu
No information about this author
et al.
ChemistrySelect,
Journal Year:
2023,
Volume and Issue:
8(20)
Published: May 24, 2023
Abstract
A
metal‐free,
straightforward,
non‐hazardous
reagent‐added,
one‐pot
approach
for
the
efficient
synthesis
of
2‐arylimino‐2
H
‐chromenes
with
high
yields
was
developed
first
time
in
this
report
through
coupling
salicylaldehydes
β‐ketothioamides,
which
catalyzed
by
lipase
water.
This
green
strategy
provides
an
method
to
obtain
various
and
enriches
practical
application
biocatalysis.
Language: Английский
Efficient Synthesis of Pyrrole Disulfides Catalyzed by Lipase in Ethanol
Feiyang Wen,
No information about this author
Yuelin Xu,
No information about this author
Fengxi Li
No information about this author
et al.
Catalysts,
Journal Year:
2023,
Volume and Issue:
13(12), P. 1493 - 1493
Published: Dec. 6, 2023
Disulfides,
as
fundamental
scaffolds,
are
widely
present
in
peptides,
natural
products,
and
pharmaceutical
molecules.
However,
traditional
synthesis
of
disulfides
often
involves
the
utilization
toxic
reagents
or
environmentally
unfriendly
reaction
conditions.
In
this
work,
a
green
efficient
method
was
developed
for
synthesizing
pyrrole
using
β-ketothioamides
ethyl
cyanoacetate
substrates,
with
lipase
serving
catalyst.
Under
optimal
conditions
(β-Ketothioamides
(1
mmol),
PPL
(200
U),
EtOH
(5
mL)),
leads
to
formation
yields
up
88%
at
40
°C.
The
related
mechanism
is
also
speculated
paper.
This
approach
not
only
presents
new
application
enzyme
catalytic
promiscuity,
but
offers
significant
advancement
synthetic
pathway
aligns
current
mainstream
research
direction
chemistry,
contributing
further
development
friendly
biocatalytic
processes.
Language: Английский