Electrochemical Synthesis of 3-(Sulfonyl)quinol-4-ones from -Alkynyl--(formyl)anilides and Sulfinates.

Electrolysis of -alkynyl--(formyl)anilides and sodium sulfinates on graphite electrodes delivers biologically sound 3-(sulfonyl)quinol-4-ones with moderate to good yields. The reaction is carried out in an undivided cell in the presence of silver(I) oxide with potassium iodide or sodium tetrafluoroborate as the supporting electrolyte. The reaction tolerates variously substituted anilides as well as aryl and alkyl sulfinates.

Extreme Tolerance of Extraocular Muscles to Diseases and Aging: Why and How?

The extraocular muscles (EOMs) possess unique characteristics that set them apart from other skeletal muscles. These muscles, responsible for eye movements, exhibit remarkable resistance to various muscular dystrophies and aging, presenting a significant contrast to the vulnerability of skeletal muscles to these conditions. In this review, we delve into the cellular and molecular underpinnings of the distinct properties of EOMs.

Azo Coupling of Indoles Revisited: Synthesis of Biindolyl Photoswitches via the Azo-Coupling/C-H Functionalization Domino Approach.

When azo coupling of aryldiazonium salts with indoles was carried out in aprotic nonpolar solvent on air, a pseudo-three-component reaction has been discovered. Azo coupling is followed by a nucleophilic addition of a second indole unit to the indolium intermediate; aromatization and oxidation are achieved under air.

Electrochemical Decarbonylative Aminosulfonylation of Alkynes with Sulfinates and -(Formyl)anilides.

An unprecedented electrochemical three-component reaction of phenylacetylene, sulfinate, and -(formyl)anilide was discovered. The transformation occurs in an undivided cell with a graphite anode and cathode in DMF in the presence of tetrabutylammonium iodide as an electrolyte. The addition of silver(I) oxide and catalytic amounts of iodine facilitated the reaction significantly.

Long-Time Non-Debye Kinetics of Molecular Desorption from Substrates with Frozen Disorder.

The experiments on the kinetics of molecular desorption from structurally disordered adsorbents clearly demonstrate its non-Debye behavior at "long" times. In due time, when analyzing the desorption of hydrogen molecules from crystalline adsorbents, attempts were made to associate this behavior with the manifestation of second-order effects, when the rate of desorption is limited by the rate of surface diffusion of hydrogen atoms with their subsequent association into molecules. However, the estimates made in the present work show that the dominance of second-order effects should be expected in the region of times significantly exceeding those where the kinetics of H desorption have long acquired a non-Debye character.