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Dive into the research topics where T. I. Godovikova is active.

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Featured researches published by T. I. Godovikova.


Russian Chemical Bulletin | 1993

Synthesis and reactivity of furazanyl- and furoxanyldiazonium salts

O. A. Rakltin; O. A. Zalesova; Alexander S. Kulikov; Nina N. Makhova; T. I. Godovikova; L. I. Khmel'nitskii

Diazotization of aminofurazans (1) and 4-aminofuroxans (2) with nitrosylsulfuric acid in a mixture of conc. H2SO4 and H3PO4 has been studied and offered as a general method for preparing furazanyl- (3) and furoxanyldiazonium (4) salts. It has been shown that reactions with the retention of the N-N-group (azo coupling, formation of triazenes and azides) are typical of salts3 and4, while elimination of the N2 molecule (Sandmeyer reaction, hydrolysis, reduction) is not typical.


Russian Journal of Applied Chemistry | 2009

Synthesis of 5-dinitromethyltetrazole

A. V. Shastin; B. L. Korsunskii; T. I. Godovikova; V. P. Lodygina

A convenient method of synthesizing 5-dinitromethyltetrazole on the basis of 1,1-diamino-2,2-dinitroehtilene was developed.


Chemistry of Heterocyclic Compounds | 1996

New method for the synthesis of 1,2,3-triazole 1-oxides

T. I. Godovikova; Svetlana P. Golova; S. A. Vozchikova; E. L. Ignat'eva; M. V. Povorin; L. I. Khmel'nitskii

A general method is proposed for the synthesis of 1,2,3-triazole 1-oxides using 3,4-dinitro- or 4-amino-3-nitrofuroxanes.


Chemistry of Heterocyclic Compounds | 2003

Reactions of 2,4-Disubstituted 5-Nitro-1,2,3-triazole 1-Oxides. 4. Dealkylation of 2-Substituted 4,5-Dinitro-1,2,3-triazole 1-Oxides

T. I. Godovikova; S. A. Vozchikova; E. L. Ignat'eva; L. I. Khmel'nitskii; B. L. Korsunskii

The N-dealkylation of 2-alkyl or 2-benzyl-substituted 4,5-dinitro-1,2,3-triazole 1-oxides has been studied. Conditions have been found for N-de-tert-butylation and 4-amino-5-nitro-1,2,3-triazole 1-oxide has been synthesized for the first time.


Russian Chemical Bulletin | 1995

Synthesis of 4,7-diaminopyridazino[4,5-c]furoxan

G. Kh. Khisamutdinov; T. A. Mratkhuzina; R. M. Gabdullin; I. Sh. Abdrakhmanov; S. P. Smirnov; Oleg A. Rakitin; T. I. Godovikova; L. I. Khmel'nitskii

Abstract4,7-Diaminopyridazino[4,5-c]furoxan was synthesized by intramolecular cyclization of 3-cyanofuroxan-4-carbamidrazone obtained from 3,4-dicyanofuroxan and hydrazine.


Russian Chemical Bulletin | 1994

REDUCTION OF THE FUROXAN RING TO THE FURAZAN RING IN SOME CARBONYL-SUBSTITUTED FUROXANS

Alexander S. Kulikov; Nina N. Makhova; T. I. Godovikova; Svetlana P. Golova; L. I. Khmel'nitskii

It was shown that the furoxan ring is efficiently reduced to the furazan ring in carbonylsubstituted furoxans with other functional groups by the action of the SnCl2-HC1-AcOH system.


Chemistry of Heterocyclic Compounds | 1994

Synthesis and nucleophilic substitution reactions of 3,4-dinitrofuroxan

T. I. Godovikova; Oleg A. Rakitin; Svetlana P. Golova; S. A. Vozchikova; M. V. Povorin; L. I. Khmel'nitskii

Abstract3, 4 Dinitrofuroxan and 3-nitrofuroxans derived from it by functional group substitution at position 4 have been synthesized for the first time.


Chemistry of Heterocyclic Compounds | 1989

Synthesis and properties of 1,2,3-triazole 1-oxides (review)

T. I. Godovikova; E. L. Ignat'eva; L. I. Khmel'nitskii

Data on the preparation, properties, and use of uncondensed 1,2,3-triazole 1-oxides are correlated for the first time.


Chemistry of Heterocyclic Compounds | 1999

Trisubstituted 1,3,5-triazines. 4. Synthesis of 2-nitroamino-4,6-bis(trinitromethyl)-1,3,5-triazine

A. V. Shastin; T. I. Godovikova; B. L. Korsunskii

The nitration, at the amino group, of 2-amino-4,6-bis(trinitromethyl)-1,3,5-triazine and its derivatives has been studied.


Chemistry of Heterocyclic Compounds | 1993

Reaction of furoxanenitrolic acids with nitrogen tetroxide

Oleg A. Rakitin; V. A. Ogurtsov; E. A. Khaibullina; T. I. Godovikova; L. I. Khmel'nitskii

It has been found that the main direction of the reaction of furoxanenitrolic acids with N2O4 is the formation of the corresponding nitrile oxides and their subsequent conversions.

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Oleg A. Rakitin

Russian Academy of Sciences

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A. V. Shastin

Russian Academy of Sciences

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B. L. Korsunskii

Russian Academy of Sciences

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Svetlana P. Golova

Russian Academy of Sciences

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S. A. Vozchikova

Russian Academy of Sciences

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Yu. A. Strelenko

Russian Academy of Sciences

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E. L. Ignat'eva

Russian Academy of Sciences

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M. V. Povorin

Russian Academy of Sciences

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V. A. Ogurtsov

Russian Academy of Sciences

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