Zobrazeno 1 - 9 of 9 pro vyhledávání: '"G. G. Shumatbaev"'
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Chiral methylbenzylammonium salts of aryldithiophosphonic acids containing glucofuranose, allofuranose, and galactopyranose diacetonide scaffolds
Autor: Yevgeniy N. Nikitin, Il'yas S. Nizamov, Oscar K. Pozdeev, Elvira S. Batyeva, Marina P. Shulaeva, G. G. Shumatbaev, Ilnar D. Nizamov, R. A. Cherkasov, Timur G. Belov
New chiral methylbenzylammonium salts of aryldithiophosphonic acids containing glucofuranose, allofuranose, and galactopyranose diacetonide substituents were obtained using (S)-(–)-α-methylbenzylamine, (R)-(+)-α-methylbenzylamine, and (R,S)-(±)-
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::619ce30f5d16f88554f711c0cd82591d
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3
Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol
Autor: G. G. Shumatbaev, Il'yas S. Nizamov, R. A. Cherkasov, D. A. Terenzhev, Ilnar D. Nizamov, Elvira S. Batyeva
Publikováno v: Russian Journal of General Chemistry. 86:564-569
Carvacrol trimethylsilyl ether when reacting with P4S10 forms S-trimethylsilyl ester of O,O-bis(5-isopropyl-2-methylphenyl)dithiophosphoric acid. The reactions of 2,4-diorganyl-1,3,2,4-dithiadiphosphetane-2,4-disulfides with carvacrol (thymol) trimet
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::20eb06b39e584d9d295b469d04a2a29c
https://doi.org/10.1134/s1070363216030117
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4
Dithiophosphorylation of nerol and geraniol trimethylsilyl derivatives
Autor: D. A. Terenzhev, Elvira S. Batyeva, Ilnar D. Nizamov, G. G. Shumatbaev, R. A. Cherkasov, Il'yas S. Nizamov
Publikováno v: Russian Journal of Organic Chemistry. 53:157-159
Reaction of tetraphosphorus decasulfide with О-(cis- and trans-3,7-dimethylocta-2,6-dien-1-yl)-trimethylsilanes affords О,О-bis(cis- and trans-3,7-dimethylocta-2,6-dien-1-yl) S-(trimethylsilyl)dithiophosphates.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6f90648b5074887f87a3df501933c4b1
https://doi.org/10.1134/s1070428017020026
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7
2,4-Diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides, their structure and S-silyl dithiophosphonic derivatives
Autor: R. A. Cherkasov, I. S. Nizamov, Ilnar D. Nizamov, G. G. Shumatbaev, D. A. Terenzhev, Daut R. Islamov, O. V. Kataeva
Publikováno v: Phosphorus, Sulfur, and Silicon and the Related Elements. 191:1576-1577
Novel 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides were prepared by the reactions of tetraphosphorus decasulfide with butylphenyl ether or 3-brominephenyl-1-isoamyl ether in 1,2-dichlorobenzene. Their structures were established by X-ray
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::71203c706e0e62f5695923b88474be4d
https://doi.org/10.1080/10426507.2016.1216417
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9
Dithiophosphorylation of paracetamol
Autor: Il'yas S. Nizamov, R. A. Cherkasov, Ilnar D. Nizamov, Elvira S. Batyeva, G. G. Shumatbaev
Publikováno v: Russian Journal of Organic Chemistry. 50:1755-1756
Paracetamol smoothly reacted with 2,4-diaryl-1,3,2λ5,4λ5-dithiadiphosphetane 2,4-disulfides to give O-[4-(acetylamino)phenyl] hydrogen arylphosphonodithioates.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4c3ecf453b3fd125f0462382b993c82e
https://doi.org/10.1134/s1070428014120069
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