A mild, scalable electrocatalytic method for direct lactonization of benzylic alcohols to phthalides using N‐hydroxyphthalimide as a redox mediator is reported. This metal‐free process proceeds via a phthalimide‐N‐oxyl‐mediated hydrogen atom transfer mechanism, shows broad scope with good to excellent yields, and enables late‐stage functionalizations ...
Pietro Ronco +6 more
wiley +1 more source
Skeletal editing of 4-arylpyrimidines into diverse nitrogen heteroaromatics via four-atom synthons. [PDF]
Li S +15 more
europepmc +1 more source
A Mild and Efficient Iridium‐Catalyzed Method for Aldimine Hydrogenation
A mild, efficient, and broadly applicable iridium‐catalyzed method for aldimine hydrogenation, facilitating access to an array of corresponding amine products in high isolated yields is reported. The developed methodology employs a bidentate iridium‐N‐heterocyclic carbene‐phosphine complex for use at low catalyst loadings, and proceeds under an ...
Aidan McKeown +4 more
wiley +1 more source
Synthesis of imidazopyridines <i>via</i> NaIO<sub>4</sub>/TBHP-promoted (3 + 2) cycloaddition and biological evaluation as anticancer agents. [PDF]
Luo H +8 more
europepmc +1 more source
Complexes of the 4d- and 5d-Groups. IV. Electron Transfer Bands with Special Application to M. Delépine's Complexes and a Transition from Iridium(III) to Pyridine, with some Remarks about Intermediate Coupling in Halide Complexes and the Uranyl Ion. [PDF]
Chr. Klixbüll Jørgensen +4 more
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This article reports an electrosynthetic method for vicinal trifluoromethylchlorosulfonylation of alkenes using [Cu(MeCN)4]PF6 and triethylamine, without elaborate ligands. The reaction efficiently adds CF3 and SO2Cl across diverse unactivated alkenes with broad functional group tolerance.
Sachini Rodrigo +2 more
wiley +1 more source
Recent Advances in Visible Light-Induced C-H Functionalization of Imidazo[1,2-a]pyridines. [PDF]
Gao J, Fu X, Yang K, Liu Z.
europepmc +1 more source
Ni Single Atoms in Zeolite Beta for Selective Alkyne Hydrogenation
Single‐atom Ni in zeolite Beta (Ni1/BEA) selectively remove trace acetylene from ethylene. Ni1/BEA achieve full conversion with ≈89% ethylene selectivity, stable for 24 h without coking, and 12 times higher TOF than prior zeolite‐supported single‐atom Ni catalysts. Na+ exchange suppress Brønsted acid‐catalyzed oligomerization. Under ethylene‐rich feeds,
Essa Alhashmi +2 more
wiley +1 more source
Pyrrolidine synthesis via ring contraction of pyridines. [PDF]
Ueno R, Hirano S, Takaya J.
europepmc +1 more source
Sulfur-containing Pyridine Derivatives. XLVI. Synthesis of 7-Bromopyrido [3, 4-d] thiazoles
Torizo Takahashi, Osamu Yamashita
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