Researchers of the Zelinsky Institute of Organic published a review on the use of oxime derivatives in selective reactions proceeding through the formation of iminyl radicals

A review article published by the researchers from the laboratory № 13 of the Zelinsky Institute of Organic Chemistry is devoted to the recent achievements in the field of free radical transformations of iminyl radicals generated from O-substituted oximes.

The strategy for using protic ionic liquids simultaneously as a solvent, acid initiator, and reagent was proposed in collaboration with the ZIOC

Researchers of laboratory № 33 of the Institute of Organic Chemistry together with scientists from the Dm. Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology, M.V. Lomonosov Moscow State University, RUDN University, N.M. Emanuel Institute of Biochemical Physics, and the Technical University of Braunschweig (Germany) published an article in which they presented a new concept of application of protic ionic liquids as triple-use reagents, namely: 1) reaction media, 2) Bronsted acids initiating various transformations due tothrough general acid catalysis, 3) nucleophiles.

Research carried out with the participation of the ZIOC scientists was noted by Synfacts

The work “Selectivity control in thiol – yne click reactions via visible light induced associative electron upconversion”, carried out within the framework of a joint international project with the participation of researchers from the Zelinsky Institute under the leadership of Academician V.P. Ananikov, was noted on the pages of Synfacts journal.