Results 81 to 90 of about 23,969 (258)
Strategic electronic matching between imidazolium salts and aryldiazonium salts enables a chromatography‐free route to versatile azoimidazolium scaffolds. Fine‐tuning the substituents unveils a powerful dichotomy: strong ─OMe resonance stabilizes highly persistent neutral aminyl radicals (up to 3 weeks), whereas the superior ─NMe2 donor strength yields
Diego Dusso +6 more
wiley +1 more source
Selective Formation of a 1,2‐Diborane(4) and Alcohol‐Driven B─B Bond Cleavage to Generate H2
Diborane(4) chemistry reveals unusual reactivity of electron‐deficient p‐block compounds. Reaction of B2Cat2 (Cat = benzene‐1,2‐diolate) with mesityllithium (MesLi; Mes = 2,4,6‐trimethylphenyl) gives a rare 1,2‐diborane(4) featuring a catecholate ligand. Alcoholysis cleaves the B─B bond and ultimately generates H2.
Rayni P. Noriega +2 more
wiley +1 more source
Synthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C-H Arylation
Direct C-H arylation coupling is potentially a more economical and sustainable process than conventional cross-coupling. However, this method has found limited application in the synthesis of organic dyes for dye-sensitized solar cells. Although direct C-
Amsalu Efrem Yemene +4 more
doaj +1 more source
An efficient synthesis of aryl(pyridyl)-methanol derivatives using Ni-NIXANTPHOS catalyzed α-arylation and tandem arylation/rearrangement is described.
Bijun Wang +8 more
core +1 more source
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
Peripheral Arylation of Subporphyrazines
AbstractPeripherally hexaarylated subporphyrazines (SubPzs) have been prepared through a Pd‐catalyzed, CuTC‐mediated coupling of a hexaethylsulfanylated subporphyrazine with arylboronic acids. The introduced aryl substituents strongly influence the electronic properties of the subporphyrazine through effective conjugative interaction.
Higashino T. +3 more
openaire +3 more sources
Palladium-catalyzed site-selective dearomative C2-arylation of 2,5-diaryl-1H-pyrroles with aryl chlorides was accomplished, and a series of 2,2,5-triaryl-2H-pyrroles were synthesized.
Sakiko Fujiwara +5 more
core +1 more source
Highly Regioselective Arylation of sp3 C−H Bonds Catalyzed by Palladium Acetate
A new palladium-catalyzed arylation process based on C−H activation has been developed. The utilization of pyridine-containing directing groups allows the β-arylation of carboxylic acid derivatives and γ-arylation of amine derivatives.
Vladimir G. Zaitsev (2669500) +2 more
core +3 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
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

