Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Timur G. Belov"'
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
Autor:
Ilnar D. Nizamov, Il'yas S. Nizamov, Elvira S. Batyeva, Alexandra D. Voloshina, R. A. Cherkasov, Timur G. Belov, Yevgeniy N. Nikitin
Publikováno v:
Heteroatom Chemistry. 27:345-352
α-d-Glucofuranose and α-d-allofuranose diacetonides react with 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides to form optically active dithiophosphonates in 78–81% yields, which are transformed into the corresponding ammonium salts in 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::798bb1dcee26250b2e73644fbcc225dc
https://doi.org/10.1002/hc.21344
https://doi.org/10.1002/hc.21344
Autor:
R. A. Cherkasov, Alexandra D. Voloshina, Yevgeniy N. Nikitin, Timur G. Belov, Ilnar D. Nizamov, Il'yas S. Nizamov
Publikováno v:
Heteroatom Chemistry. 27:108-113
The reaction of 2,4-diaryl 1,3,2,4-dithiadiphosphetane-2,4-disulfide with diketonide of d-mannitol has been found to give optically active bisaryldithiophosphonic acids transformed into the corresponding diammonium salts by the treatment of n-hexadec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf33e47c540e1e19dac0ea1c5cfb892f
https://doi.org/10.1002/hc.21307
https://doi.org/10.1002/hc.21307