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Dive into the research topics where L. A. Kiprianova is active.

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Featured researches published by L. A. Kiprianova.


Journal of Fluorine Chemistry | 1995

Electrochemical initiation by sulfur dioxide of radical-chain trifluoromethylation processes of thiophenols with bromotrifluoromethane

V. G. Koshechko; L. A. Kiprianova; Ludmyla I. Fileleeva; Z.Z. Rozhkova

Abstract Sulfur dioxide may serve as an efficient catalyst for the electrochemical trifluoromethylation of thiophenols by Freon F13B1 (CF 3 Br), which enables implementation of trifluoromethylation in an energy-saving radical-chain regime.


Journal of Fluorine Chemistry | 1999

Fluoroalkylation of thiophenols with Freons using conjugated electron transfer mediator systems composed of methylviologen-SO2 and I2-SO2

V. G. Koshechko; L. A. Kiprianova; Ludmyla I. Fileleeva; K.G Tsanov

Abstract Methylviologen-sulfur dioxide and iodine (iodide)-sulfur dioxide have been shown to mediate electron transfer from thiophenols to Freons and perform the fluoroalkylation of thiophenols under mild conditions.


Theoretical and Experimental Chemistry | 1994

Sulfur dioxide electrocatalysis of radical-chain trifluoromethylation of thiophenols by bromotrifluoromethane

V. G. Koshechko; L. A. Kiprianova; L. I. Fileleeva; Z. Z. Rozhkova

The possibility of electrocatalysis by sulfur dioxide has been demonstrated in the trifluoromethylation of thiophenols by Freon F13B1 (CF3Br) to form trifluoromethyl aryl sulfides. A study has been made of the influence of the mediator concentration, the electronic structure of the thiophenol, and the electrolysis conditions on the course of the trifluoromethylation process.


Theoretical and Experimental Chemistry | 1998

Activation of freons by cascade electron transfer from a nucleophile using two mutually complementary mediators—Methylviologen and sulfur dioxide

V. G. Koshechko; L. A. Kiprianova; L. I. Fileleeva; K. G. Tsanov

It was shown that a system consisting of two mutually complementary electron transfer mediators (methylviologen and sulfur dioxide) is capable of bringing about cascade electron transfer from thiophenols to Freons (CF3Br, CF2ClCCl2F), activating the latter under mild conditions, and bringing them into fluoroalkylation.


Theoretical and Experimental Chemistry | 1996

Electrochemical functionalization of phenothiazine by nitrogen-containing heterocycles

V. G. Koshechko; Ludmyla I. Kalinina; L. A. Kiprianova; V. D. Pokhodenko

We demonstrate the feasibility of electrochemically activated introduction of pyridine and nicotinarnide into the aromatic ring of phenothiazine with formation of N-(3-phenothiazinyl)-pyridinium perchlorate and N-(3-phenothiazinyl)-3-carbamide-pyridinium perchlorate. We have studied the physicochemical properties of the derivatives obtained.


Journal of Fluorine Chemistry | 2006

Polyfluoroalkylation of 2,6-di-tert-butylphenol by 1,2-dibromotetrafluoroethane activated by sulfur dioxide

V. G. Koshechko; L. A. Kiprianova; Ludmyla I. Fileleeva; Ludmyla I. Kalinina; Vasylii A. Khizhnyi


Journal of Fluorine Chemistry | 2010

Activation of free-radical polyfluoroalkylation of organic substrates with freon BrCF2CF2Br using a system of organic base-electron transfer mediator

V. G. Koshechko; L. A. Kiprianova; Ludmyla I. Kalinina


Journal of Fluorine Chemistry | 2009

Chain-radical fluoroalkylation of thiophenols with freon ClCF2CFCl2 in the presence of sulfur dioxide

V. G. Koshechko; L. A. Kiprianova; Ludmyla I. Kalinina


Journal of Fluorine Chemistry | 2007

Selective fluoroalkylation of thiophenols by 1,2-dibromotetrafluoroethane activated by sulfur dioxide

V. G. Koshechko; L. A. Kiprianova; Ludmyla I. Fileleeva; Ludmyla I. Kalinina


Russian Chemical Bulletin | 2010

Polyfluoroalkylation of pyrrole with 1,2-dibromotetrafluoroethane activated by sulfur dioxide

V. G. Koshechko; L. A. Kiprianova; Ludmyla I. Kalinina

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V. G. Koshechko

National Academy of Sciences of Ukraine

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Ludmyla I. Kalinina

National Academy of Sciences of Ukraine

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Ludmyla I. Fileleeva

National Academy of Sciences of Ukraine

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K.G Tsanov

National Academy of Sciences of Ukraine

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Vasylii A. Khizhnyi

National Academy of Sciences of Ukraine

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