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Svetlana V. Amosova

Researcher at Russian Academy of Sciences

Publications -  420
Citations -  2621

Svetlana V. Amosova is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Selenium & Selenide. The author has an hindex of 24, co-authored 407 publications receiving 2311 citations. Previous affiliations of Svetlana V. Amosova include Russian Academy & Saint Petersburg State University.

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Addition of selenium dibromide to divinyl sulfide: spontaneous rearrangement of 2,6-dibromo-1,4-thiaselenane to 5-bromo-2-bromomethyl-1,3-thiaselenolane

TL;DR: In this paper, the synthesis of the selenium heterocycles 1, 2, and 3 based on the addition reaction of Selenium dibromide to divinyl sulfide is described.
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Thia-, Aza-, and Selena[3.3.1]bicyclononane Dichlorides: Rates vs Internal Nucleophile in Anchimeric Assistance

TL;DR: Compared substitution rates forulfur-, selenium-, and nitrogen-containing compounds bearing leaving groups in the β-position undergo facile substitution chemistry enabled by anchimeric assistance, showing that the process is controlled by the formation of the high-energy three-membered cationic intermediate.
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A palladium complex with a new hemilabile amino- and sulfur-containing phosphinite ligand as an efficient catalyst for the Heck reaction of aryl bromides with styrene. The effect of the amino group

TL;DR: In this article, a palladium complex with a new hemilabile amino-and sulfur-containing phosphinite ligand has been synthesized and its crystal structure determined, which efficiently catalyses the Heck reaction of aryl bromides with styrene at 130°C after 24h.
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New Palladium Complexes with S‐ or Se‐Containing Schiff‐Base Ligands as Efficient Catalysts for the Suzuki–Miyaura Cross‐Coupling Reaction of Aryl Bromides with Phenylboronic Acid under Aerobic Conditions

TL;DR: In this paper, four palladium chelate complexes with S- or Se-containing substituted salicylaldehyde Schiff base derivatives have been synthesized, which are thermally and air stable and efficiently catalyze the Suzuki-Miyaura crosscoupling of aryl bromides with phenylboronic acid in air.