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News and Announcements

2021, April, 19

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.

2021, April, 15

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.

2021, April, 12

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.

2021, April, 05

Scientists from ZIOC developed a photocatalytic method for alkenes homologization

Researchers from the Laboratory № 8 of the ZIOC found that readily available triphenylphosphonium triflate could enter photocatalytic hydrophosphination of unactivated alkenes.

2021, April, 01

Scientists of the Zelinsky Institute published the review on asymmetric aza-Diels-Alder reactions

The review published by scientists from laboratory № 11 of the Institute of Organic Chemistry is devoted to the latest achievements in the field of catalytic asymmetric aza-Diels-Alder reactions.

2021, March, 25

A new class of fluorophores was developed in ZIOC RAS

Scientists from the Laboratory № 6 of the Zelinsky Institute have synthesized a new class of fluorophores based on 5-hydroxyisoquinolone derivatives.

2021, March, 22

Researchers of the Zelinsky Institute conducted the study on the dependence of the selectivity of liquid-phase hydrogenation of substituted alkynes from the size of Pd nanoparticles

The latest work of the laboratory № 35 of the Zelinsky Institute is devoted to a detailed study of the effect of the size of Pd nanoparticles on the course of liquid-phase hydrogenation of substituted alkynes.

2021, March, 15

An effective method for the synthesis of inhibitors of aldoketo reductase 1B10 was developed in the Zelinsky Institute

Using the SRR approach, a group of researchers from the Zelinsky Institute of Organic Chemistry developed a pseudo-four-component method for the synthesis of polyheterocyclic compounds containing chromene, pyridine, and pyrazole fragments.

2021, March, 11

Scientists from the Zelinsky Institute succeeded in the effective deuteration of organic compounds without the use of metal salts.

Scientists from Laboratory № 30 of the ZIOC developed a new organocatalytic approach to deuteration of a wide range of weak CH-acids using acetone-d6 as a source of the deuterium atom, as well as N-alkylimidazolium salts and oxygen-containing bases.

2021, March, 04

The results of research by scientists from the Zelinsky Institute are placed on the cover of highly-impacted journal of the American Chemical Society

Researchers from the Laboratory № 14 of the ZIOC with the support of the Russian Science Foundation (grant № 17-73-20282) developed a unique catalytic system based on mixed cerium-zirconium oxide-supported platinum clusters for the selective hydrogenation of various organic compounds under mild conditions.