I. Sh. Salikhov
Russian Academy of Sciences
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Russian Chemical Bulletin | 1995
V. S. Reznik; I. Sh. Salikhov; Yu. S. Shvetsov; Yu. Ya. Efremov; I. Kh. Rizvanov
Methods for the synthesis of compounds containing two or more pyrimidine rings linked through aliphatic chains with different numbers of carbon atoms are described.
Russian Chemical Bulletin | 1986
I. Sh. Salikhov; V. S. Reznik; Yu. S. Shvetsov; V. V. Petrova; R. R. Shagidullin
ConclusionsA method has been developed for the preparation of 1,3-bis(ω-haloalkyl)uracils with methylene chains of different lengths in the ω-haloalkyl radicals in the N1 and N3 positions of the pyrimidine ring.
Russian Chemical Bulletin | 1989
I. Sh. Salikhov; V. O. Kuznetsov; V. S. Reznik
A method was developed for obtaining previously unknown 1,3,7-tris(ω-haloalkyl)-, 1,7-bis(ω-chloroalkyl)-3-methyl-, and 1,3-bis(ω-chloropentyl)-7-methylxanthines.
Russian Chemical Bulletin | 1986
I. Sh. Salikhov; V. S. Reznik; Yu. S. Shevtsov; R. R. ShagidullinJr.
Conclusions1.The reaction of Na salts of certain aminohydroxypyrimidines with α,ω-dihaloalkanes has been studied. A one-stage method of preparation of 4-(ω-haloalkyloxy)aminopyrimidines has been developed.2.The sodium salt of 5,5-diethylbarbituric acid reacts with α,ω-dihaloalkanes to form N-(ω-haloalkyl); and l,3-bis(ω-haloalkyl)-5,5-diethylbarbituric acids.
Russian Chemical Bulletin | 1980
V. S. Reznik; I. Sh. Salikhov; Yu. S. Shvetsov; B. E. Ivanov
Conclusions1.The reaction of the Na salts of hydroxypyrimidines withα,ω-dibromoalkanes gives, besides N-(ω-bromoalkyl)dihydrooxopyrimidines, also the intermolecular transalkylation products.2.The structures of the products obtained by reacting equimolar amounts of the Na salt of 6-methyluracil andα,ω-dibromoalkanes, with a variable number of methylene groups between the bromine atoms, were established and the reasons for the predominant formation of oligomeric products in the given reactions were discussed.
Russian Chemical Bulletin | 1977
V. S. Reznik; I. Sh. Salikhov; Yu. S. Shvetsov; A. N. Shirshov; V. S. Bakulin; B. E. Ivanov
A simple one-step method for the synthesis of 1,3-bis(ω-haloalkyl)uracils by reacting the Na salts of uracil and its derivatives with α,ω-dihaloalkanes has been developed.
Russian Chemical Bulletin | 1975
V. S. Reznik; Yu. S. Shvetsov; V. S. Bakulin; I. Sh. Salikhov
ChemInform | 2010
V. S. Reznik; I. Sh. Salikhov; Yu. S. Shvetsov; A. N. Shirov
ChemInform | 1990
I. Sh. Salikhov; V. O. Kuznetsov; V. S. Reznik
ChemInform | 1987
I. Sh. Salikhov; V. S. Reznik; Yu. S. Shvetsov; V. V. Petrova; R. R. Jun. Shagidullin