33 research outputs found
One-Pot Synthesis of Polysubstituted Spirofluorene–Indene via Ru(II)-Catalyzed [3 + 2] Annulation and Intramolecular Friedel–Crafts Cyclization
RuÂ(II)-catalyzed
one-pot synthesis of polysubstituted spirofluorene–indenes
via [3 + 2] annulation and then intramolecular Friedel–Crafts
alkylation has been achieved. The simple method provides a broad scope
of aryl ketones and internal alkynes, achieving PAHs skeletons in
moderate to good yields
Formation of Fluorovinyl Spiro-[imidazole-indene] and α‑Amino-β-naphthalenones via Rh(III)-Catalyzed Cascade C–H Functionalization
An efficacious method for building fluorovinyl spiro-[imidazole-indene]
and α-amino-β-naphthalenone skeletons synchronously has
been shown to consist of Rh(III)-catalyzed C–H functionalization
between 2H-imidazoles and difluoromethylene alkynes.
This protocol demonstrates a practical and straightforward route for
installing fluorine elements in the envisioned position of heterocyclic
compounds
sj-docx-1-oss-10.1177_01708406231162000 – Supplemental material for Amplifying Stigmatization: Owlcatraz and the naming of a football stadium
Supplemental material, sj-docx-1-oss-10.1177_01708406231162000 for Amplifying Stigmatization: Owlcatraz and the naming of a football stadium by Lin Dong, Bryant Ashley Hudson, David Moura and Lee C. Jarvis in Organization Studies</p
Cobalt(III)-Catalyzed C–H Amidation of 7‑Azaindoles with Dioxazolones: Synthesis of 7‑Azaindole Amidated Derivatives
An efficient cobalt-catalyzed
C–H amidation of 7-azaindoles was developed by using dioxazolones
as the amidating reagent. A wide scope of substituted 7-azaindoles,
even <i>N</i>-vinly groups, is suitable for the reaction,
generating 7-azaindoles derivatives with potential properties up to
91% yield under straightforward and strong applicable reaction conditions
Organocatalytic Sequential Hetero-Diels–Alder and Friedel–Crafts Reaction: Constructions of Fused Heterocycles with Scaffold Diversity
A highly enantioselective aza-Diels–Alder and Friedel–Crafts reaction sequence of <i>N</i>-sulfonyl-1-aza-1,3-butadienes and aliphatic aldehydes tethered to an arene motif has been developed, affording the fused chiral piperidine frameworks with a versatile scaffold diversity. A similar strategy has been applied for the construction of complex chiral tetrahydroquinoxaline structures
Highly Functionalized Pyridines Synthesis from <i>N</i>‑Sulfonyl Ketimines and Alkynes Using the N–S Bond as an Internal Oxidant
The
N–S bond-based internal oxidant offers a distinct approach
for the synthesis of highly functionalized pyridines. A novel RhÂ(III)-catalyzed
one-pot process undergoes an efficient C–C/C–N bond
formation along with desulfonylation under very mild conditions. The
method is quite simple, general, and efficient
Rhodium(III)-Catalyzed Oxidative Annulation of 7‑Azaindoles and Alkynes via Double C–H Activation
RhodiumÂ(III)-catalyzed double C–H
activation involving <i>N</i>-directed <i>ortho</i> C–H activation
and subsequent <i>roll-over</i> C–H activation of
the heterocycle ring has been developed to form complex 7-azaindole
derivatives in moderate to excellent yields. A broad scope of 7-azaindoles
and internal alkynes has been demonstrated in this oxidative annulation
reaction
Mechanically Induced Light Emission and Infrared-Laser-Induced Upconversion in the Er-Doped CaZnOS Multifunctional Piezoelectric Semiconductor for Optical Pressure and Temperature Sensing
In
this study, we report an Er-doped quaternary piezoelectric semiconductor
CaZnOS:Er<sup>3+</sup> which shows both mechanoluminescence and upconversion
luminescence properties. Under mechanical stimulation, green light
emission can be observed by the naked eye from a flexible film fabricated
by encapsulating CaZnOS:Er<sup>3+</sup> particles between two polyethylene
glycol terephthalate substrates. The integral emission intensity is
proportional to applied pressure, making CaZnOS:Er<sup>3+</sup> suitable
for dynamic pressure sensing applications. Moreover, the doped sample
also shows bright visible emission with near-infrared (980 nm) excitation.
The fluorescence intensity ratio between two upconversion emission
bands corresponding to <sup>2</sup>H<sub>11/2</sub>, <sup>4</sup>S<sub>3/2</sub> → <sup>4</sup>I<sub>15/2</sub> transitions of Er<sup>3+</sup> is sensitive to the variation of temperature. As a multifunctional
optical material, CaZnOS:Er<sup>3+</sup> could be used to not only
visualize two-dimensional pressure distribution, through mechanically
induced emission, but also sense temperature via the upconversion
(UC) luminescence. This work provides a novel kind of multifunctional
luminescent material for the development of integrated and coupling
devices
Aminocatalytic Asymmetric <i>exo</i>-Diels–Alder Reaction with Methiodide Salts of Mannich Bases and 2,4-Dienals to Construct Chiral Spirocycles
An asymmetric <i>exo</i>-Diels–Alder reaction of α-methylene carbonyl compounds, generated in situ from stable methiodide salts of Mannich bases, with 2,4-dienals, has been developed through trienamine activation of a chiral secondary amine. A spectrum of spirocyclanes with high molecular complexity was efficiently constructed in moderate to excellent diastereo- and enantioselectivity