V. G. Chilikin
A. N. Nesmeyanov Institute of Organoelement Compounds
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Russian Chemical Bulletin | 1996
A. V. Fokin; Yu. N. Studnev; V. P. Stolyarov; V. G. Chilikin; G. A. Prigorelov
The addition of sulfur chloride pentafluoride to various terminal olefins, including those containing functional substituents, was studied. Possible side processes in these reactions are oligomerization and fluorination of the starting olefin.
Russian Chemical Bulletin | 1986
A. V. Fokin; A. I. Rapkin; V. G. Chilikin; O. V. Verenikin; Yu. N. Studnev
Conclusions1.Addition of nitrosyl fluorosulfate to the multiple bond of fluoroolefins was accomplished, and the previously unknown 2-nitrosopolyfluoroalkyl fluorosulfates were obtained.2.It was shown that 2-nitrosopolyfluoroalkyl fluorosulfates are effective dienophiles, and in reaction with fluoroolefins at 20–50‡C they form the corresponding oxazetidines and nitrosofluoropolymers.
Russian Chemical Bulletin | 1985
A. V. Fokin; Yu. N. Studnev; A. I. Rapkin; V. G. Chilikin; O. V. Verenikin
Conclusions1.In reactions of bromine tris (fluorosulfate) with fluoroolefins the corresponding 2-bromofluoroalkyl fluorosulfates and vicinal bis (fluorosulfonyloxy) fluoroalkanes, products of addition to the multiple bond of elements of bromine monofluorosulfate and peroxydisulfuryl difluoride, respectively, are formed.2.Bromine tris (fluorosulfate) substitutes H and Cl atoms for the fluorosulfate groups in freons.
ChemInform | 1984
A. V. Fokin; Yu. N. Studnev; A. I. Rapkin; I. N. Krotovich; V. G. Chilikin; O. V. Verenikin
ConclusionsThe replacement of the nitroso group in perfluoronitrosoalkanes in the presence of chlorine fluorosulfate and peroxydisulfuryl difluoride was studied. A hypothesis concerning the possible reaction mechanism was stated.
Russian Chemical Bulletin | 1983
A. V. Fokin; Yu. N. Studnev; A. I. Rapkin; V. G. Chilikin; O. V. Verenikin
ConclusionsWe were the first to add nitronium fluosulfate to the multiple bond of fluoroolefins to give the corresponding fluorinated β-nitroalkyl fluosulfates. The theory was expressed that the electrophilic mechanism applies to the given process.
ChemInform | 1986
A. V. Fokin; A. I. Rapkin; V. G. Chilikin; O. V. Verenikin; Yu. N. Studnev
Russian Chemical Bulletin | 1985
A. V. Fokin; Yu. N. Studnev; A. I. Rapkin; V. G. Chilikin; O. V. Verenikin
Russian Chemical Bulletin | 1984
A. V. Fokin; Yu. N. Studnev; A. I. Rapkin; V. G. Chilikin
ChemInform | 1984
A. V. Fokin; Yu. N. Studnev; A. I. Rapkin; V. G. Chilikin; O. V. Verenikin
ChemInform | 1983
A. V. Fokin; Yu. N. Studnev; A. I. Rapkin; V. G. Chilikin; A. S. Tatarinov