Results 91 to 100 of about 3,271,959 (246)
Hypervalent Iodine Phenol Dearomatization Mediated by Mechanochemistry
A solvent‐free mechanochemical process has been developed that enables the rapid oxidative dearomatization of phenols. This method produces spiranic dienones with decent to good yields. This process eliminates the need for expensive and environmentally harmful perfluorinated alcohols, such as hexafluoroisopropanol and trifluoroethanol, while adhering ...
Jérémie Cuillerier +3 more
wiley +1 more source
C-C bond forming reactions are central to the construction of π-conjugated polymers. Classical C-C bond forming reactions such as the Stille and Suzuki coupling reactions have been widely used in the past for this purpose.
Arthur D. Hendsbee, Yuning Li
doaj +1 more source
Direct α-C(sp<sup>3</sup>)─H Alkylation and Arylation of Ethers Enabled by Carbon Nitride/Nickel Metallaphotoredox Catalysis. [PDF]
A recyclable carbon nitride/nickel metallaphotoredox platform enables direct α‐C(sp3)─H arylation and alkylation of ethers, amides, and benzylic substrates under visible light. Broad substrate scope, late‐stage functionalization, five‐cycle photocatalyst reuse, and continuous‐flow translation are demonstrated, while mechanistic studies support ...
de Vries Ibáñez MM +8 more
europepmc +2 more sources
Abstract Organic electronics have emerged as a key class of functional materials for organic light‐emitting diodes (OLEDs), organic photovoltaics (OPVs), organic field‐effect transistors (OFETs), sensors, and printed electronics. However, commercialization remains dependent on the ability to reproducibly synthesize and manufacture high‐performance ...
Marko D. Saban, Benoît H. Lessard
wiley +1 more source
2-Pyridone ligand-facilitated palladium-catalyzed direct C–H bond functionalization via the transient directing group strategy has become an attractive topic.
Ziting Xu +4 more
doaj +1 more source
Extending the utility of [Pd(NHC)(cinnamyl)Cl] precatalysts: Direct arylation of heterocycles
The use of [Pd(NHC)(cinnamyl)Cl] precatalysts in the direct arylation of heterocycles has been investigated. Among four different precatalysts, [Pd(SIPr)(cinnamyl)Cl] proved to be the most efficient promoter of the reaction.
Anthony R. Martin +3 more
doaj +1 more source
Rh(I)-Catalyzed Direct Arylation of Azines
The Rh(I)-catalyzed direct arylation of azines has been developed. Quinolines and 2-substituted pyridines couple with aryl bromides to efficiently afford ortho-arylated azine products using the commercially available and air-stable catalyst [RhCl(CO)2]2.
Robert G. Bergman (1323120) +2 more
core +1 more source
we have developed an electrochemical Ni−H catalyzed arylation coupling method of unactivated alkenes with aryl halides. The method displays broad functional group tolerance and proceeds under very mild conditions. Furthermore, aryl chlorides were also compatible substrates in this catalytic system. This conversion holds significant implications for the
Chao Xu, Ru‐Han A, Xiao‐Feng Wu
wiley +1 more source
Regioselective copper-catalyzed direct arylation of benzodithiophene-S,S-tetraoxide
An efficient copper-catalyzed direct arylation reaction for the regioselective functionalization of benzodithiophene-S,S-tetraoxide has been developed.
A. L. Rheingold +3 more
core +1 more source
Ullmann‐Type N‐Heteroarylation of Nitrogen Heterocycles Catalyzed by Heterogeneous CuNPs/HKUST‐1
A practical strategy for the direct synthesis of CuNPs/HKUST‐1 heterogeneous catalyst was developed and used for the catalyzing Ullmann‐type N‐arylation of N‐heterocycles with high yields, excellent recyclability, and low copper leaching. ABSTRACT Ullmann‐type C–N coupling is an essential reaction to construct functional nitrogen heterocycles, whereas ...
Shuai Yang +9 more
wiley +1 more source

