Zobrazeno 1 - 7
of 7
pro vyhledávání: '"E. Kh. Pulatov"'
Autor:
M. I. Jumaeva, E. Kh. Pulatov, B. G. Mavlonov, M. Z. Turdialiev, M. D. Isobaev, T. Kh. Abdullaev
Publikováno v:
Russian Journal of Organic Chemistry. 57:369-375
The hydrolysis of 2-methylbut-3-yn-2-yl carbamate gave 4,4-dimethyl-5-methylidene-1,3-dioxolan-2-one, whereas 2-methylbut-3-yn-2-ol was converted under similar conditions to 3-hydroxy-3-methylbutan-2-one. 2-[2-Amino(hydrazinyl)-6H-1,3,4-thiadiazin-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::892063f7c823793bc4d967a984aec21e
https://doi.org/10.1134/s1070428021030076
https://doi.org/10.1134/s1070428021030076
Publikováno v:
Russian Chemical Bulletin. 67:1106-1109
The reactions of thiosemicarbazide (TSC), thiocarbohydrazide, and hydrazine thiocarbamate with oxyketones, haloketones, and derivatives of acetylenic alcohols were studied. Thiadiazines bearing exocyclic thio and hydrazo groups were synthesized. Acet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ef963cc61bb089db3f867d17ba64dbd
https://doi.org/10.1007/s11172-018-2188-2
https://doi.org/10.1007/s11172-018-2188-2
Publikováno v:
Russian Chemical Bulletin. 65:2475-2478
Cyclocondensation of 1-hydroxyketones with thiosemicarbazide resulted in thiadiazines. Nitrate ester of 1-hydroxyketone reacted under similar conditions to give the corresponding thiosemicarbazone. In the case of bromoacetyl-substituted nitrate ester
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91d26ce8ca6ab38dda11fdb90dc6d0ca
https://doi.org/10.1007/s11172-016-1609-3
https://doi.org/10.1007/s11172-016-1609-3
Autor:
E. Kh. Pulatov, M. D. Isobaev
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d00dfff3387389ee4ccddd7315bafa70
https://doi.org/10.1002/chin.199723151
https://doi.org/10.1002/chin.199723151
Autor:
E. Kh. Pulatov, M. D. Isobaev
Publikováno v:
ChemInform. 29
Thiazolidinethiones react with hydrazine hydrate to give bicyclic compounds with a bridge sulfur atom. The bicyclic structure of the reaction products is confirmed by data from1H NMR and IR spectroscopy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b4228c91977bcce4510681889dd9b1e
https://doi.org/10.1002/chin.199817175
https://doi.org/10.1002/chin.199817175
Autor:
M. D. Isobaev, E. Kh. Pulatov
Publikováno v:
Russian Chemical Bulletin. 45:2820-2822
The major reaction center in the reaction of 4,4-dialkyl-5-methylene-2-phenyliminothiazolidines with acid chlorides or anhydrides and with arenesulfonyl chlorides is the nitrogen atom at position 3 of the ring.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15558eeb1b08254a4fe3e5405dcf393c
https://doi.org/10.1007/bf01430651
https://doi.org/10.1007/bf01430651
Autor:
E. Kh. Pulatov, M. D. Isobaev
Publikováno v:
Russian Chemical Bulletin. 47:173-174
Thiazolidinethiones react with hydrazine hydrate to give bicyclic compounds with a bridge sulfur atom. The bicyclic structure of the reaction products is confirmed by data from1H NMR and IR spectroscopy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6cc2d7561cc6d9471b240c4c9db45b0
https://doi.org/10.1007/bf02495527
https://doi.org/10.1007/bf02495527