6 research outputs found
Design of Highly Stable Iminophosphoranes as Recyclable Organocatalysts: Application to Asymmetric Chlorinations of Oxindoles
A new family of tartaric
acid derived chiral iminophosphoranes
has been developed as highly effective organocatalysts in the asymmetric
chlorinations of 3-substituted oxindoles with a high level of enantioselectivity.
Importantly, these catalysts are air- and moisture-stable. Recovery
of the catalyst after simple chromatographic separation for reuse
in the model reaction was achieved; the catalyst can be recycled six
times without loss of any enantioselectivity. Several advantages of
this catalytic process are high conversion after a very short reaction
time at ambient temperature, low catalytic loading, and scale-up to
multigram quantities with an excellent enantiomeric excess value of
>99%, which meets the enantiomeric purity required for pharmaceutical
purposes
Palladium Catalyzed C–I and Vicinal C–H Dual Activation of Diaryliodonium Salts for Diarylations: Synthesis of Triphenylenes
Using
the synthetic strategy of palladium-catalyzed dual activation
of both C–I and vicinal C–H bonds of diaryliodonium
salts, we report an approach for direct diarylations of 2-bromobiphenyls
or bromobenzenes. As a result, a wide range of triphenylenes with
various substituents have been synthesized in good yields. These triphenylenes
are expected to be employed in the “bottom-up” synthesis
of functional aromatic molecules in material science
Palladium-Catalyzed Double-Suzuki–Miyaura Reactions Using Cyclic Dibenziodoniums: Synthesis of <i>o</i>‑Tetraaryls
Palladium-catalyzed double-Suzuki–Miyaura
couplings between
cyclic dibenziodoniums and arylboronic acids have been developed.
As such, a wide range of <i>o</i>-tetraaryls were synthesized
in good to excellent yields of 22–94%. Furthermore, tetraphenylene
was prepared in 21% isolated yield with 2,2′-biphenyldiboronic
acid by using this method
Palladium Catalyzed C–I and Vicinal C–H Dual Activation of Diaryliodonium Salts for Diarylation: Synthesis of 4,5-Benzocoumarins
With a strategy that
makes use of palladium activation of both
C–I and vicinal C–H bonds of diaryliodonium salts, an
unprecedented approach in diarylation of coumarins was reported. As
such, a wide range of 4,5-benzocoumarins with potential fluorescence
properties have been synthesized in good yields. A series of experiments
suggested that the formation of two carbon–carbon bonds proceeded
in a synergetic manner
Synthesis of 2,3-Disubstituted <i>NH</i> Indoles via Rhodium(III)-Catalyzed C–H Activation of Arylnitrones and Coupling with Diazo Compounds
A rhodium-catalyzed intermolecular
coupling between arylnitrones
and diazo compounds by C–H activation/[4 + 1] annulation with
a CÂ(N<sub>2</sub>)–CÂ(acyl) bond cleavage is reported, and 2,3-disubstituted <i>NH</i> indoles are directly synthesized in up to a 94% yield.
A variety of functional groups are applicable to this reaction to
give the corresponding products with high selectivity. Compared to
other previously reported RhÂ(III)-catalyzed synthesis of homologous
series, this method is simpler, more general, and more efficient
High-Performance Cable-Type Flexible Rechargeable Zn Battery Based on MnO<sub>2</sub>@CNT Fiber Microelectrode
Nowadays, linear-shaped
batteries have received increasing attentions because the unique one-dimensional
architecture offers an omni-directional flexibility. We developed
a cable-type flexible rechargeable Zn microbattery based on a microscale
MnO<sub>2</sub>@carbon nanotube fiberlike composite cathode and Zn
wire anode. The Zn–MnO<sub>2</sub> cable microbattery exhibits
a large specific capacity, good rate performance, and cyclic stability.
The capacity of Zn–MnO<sub>2</sub> cable batteries are 322
and 290 mAh/g based on MnO<sub>2</sub> with aqueous and gel polymer
electrolyte, corresponding to the specific energy of 437 and 360 Wh/kg,
respectively. Besides, the Zn–MnO<sub>2</sub> cable battery
shows excellent flexibility, which can be folded into arbitrary shapes
without sacrificing electrochemical performance. Furthermore, we studied
electrochemical properties of Zn–MnO<sub>2</sub> cable microbatteries
with different Zn salt electrolytes, such as Zn salt with small anions
(ZnSO<sub>4</sub> or ZnCl<sub>2</sub>, etc.) and Zn salt with bulky
anions (ZnÂ(CF<sub>3</sub>SO<sub>3</sub>)<sub>2</sub>, etc.). With
the merits of impressive electrochemical performance and flexibility,
this first flexible rechargeable Zn–MnO<sub>2</sub> cable-like
battery presents a new approach to develop high-performance power
sources for portable and wearable electronics