Zobrazeno 1 - 10
of 10
pro vyhledávání: '"S. L. Deev"'
Publikováno v:
Chimica Techno Acta, Vol 2, Iss 2, Pp 158-163 (2015)
New analogues of acyclovir have been prepared by reacting 1,2,4-triazolo[1,5-a]pyrimidin-7-ones 1а-i and (2-acetoxyethoxy)methyl acetate 2 in the presence of trimethylsilyl trifluoromethanesulfonate as a catalyst. Thei nteraction between the compoun
Externí odkaz:
https://doaj.org/article/417bf516e5d54639ab869d7f7d88b5ed
Publikováno v:
Chimica Techno Acta, Vol 2, Iss 2, Pp 158-163 (2015)
New analogues of acyclovir have been prepared by reacting 1,2,4-triazolo[1,5-a]pyrimidin-7-ones 1а-i and (2-acetoxyethoxy)methyl acetate 2 in the presence of trimethylsilyl trifluoromethanesulfonate as a catalyst. Thei nteraction between the compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c0aaa98cf1a2db12198e6df5496ebf2
https://doi.org/10.15826/chimtech.2015.2.2.017
https://doi.org/10.15826/chimtech.2015.2.2.017
Autor:
S. L. Deev, T. S. Shestakova, Oleg I. Kiselev, Rusinova Larisa I, E. G Deeva, O. N. Chupakhin, E. N. Ulomskii, Vladimir L. Rusinov
Publikováno v:
Russian Chemical Bulletin. 59:136-143
Nucleoside analogs containing hydroxybutyl, hydroxyethoxymethyl, allyloxymethyl, and propargyloxymethyl fragments were synthesized based on 1,2,4-triazolo[3,2-c][1,2,4]triazin-7-ones isosteric to purine bases. Some of the compounds obtained inhibit i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a07b320aeda3e9bd90e979c971c8318c
https://doi.org/10.1007/s11172-010-0056-9
https://doi.org/10.1007/s11172-010-0056-9
Publikováno v:
Russian Chemical Bulletin. 54:726-732
A new in principle method for the synthesis of 6-aryl(hetaryl)-3,5-diamino-1,2,4-triazines by decomposition of pre-synthesized tetrazolo[1,5-b][1,2,4]triazines was developed. The advantages of this method over traditional methods were demonstrated us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22e26c3908d7ac1b475ab5ed8093fc32
https://doi.org/10.1007/s11172-005-0311-7
https://doi.org/10.1007/s11172-005-0311-7
Publikováno v:
Russian Chemical Bulletin. 51:1737-1743
The replacement of the amino group with the hydroxy group was examined in the series of 6-aryl- and 6-benzoimidazolyl-7-aminoazolo[5,1-c]-1,2,4-triazines. These reactions provide a convenient synthetic procedure for the preparation of fused azolo[5,1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5de47aa624bffb8bb55300d94abf282b
https://doi.org/10.1023/a:1021320025860
https://doi.org/10.1023/a:1021320025860
Publikováno v:
Russian Journal of Organic Chemistry. 38:272-280
Reaction of 3-nitro- and 3-ethoxycarbonyl-1,2,4-triazolo[5,1-c]-1,2,4-triazin-4-ones with 1-adamantanol (or 1-adamantyl nitrate) in concentrated sulfuric acid or with 1-bromoadamantane in sulfolane affords N-adamantyl derivatives. The adamantylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad69b44540a87220838a4ce11419ea31
https://doi.org/10.1023/a:1015538322029
https://doi.org/10.1023/a:1015538322029
Publikováno v:
Synthetic Communications. 31:2351-2355
A general method for inclusion of the 15N label into the position 1 of 6-nitro-1,2,4-triazolo[5,1-c][1,2,4]triazin-7-one by using K15NO3 has been developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::199906e28fed4c00aa2a680095789786
https://doi.org/10.1081/scc-100104836
https://doi.org/10.1081/scc-100104836
Publikováno v:
ChemInform. 33
Reaction of 3-nitro- and 3-ethoxycarbonyl-1,2,4-triazolo[5,1-c]-1,2,4-triazin-4-ones with 1-adamantanol (or 1-adamantyl nitrate) in concentrated sulfuric acid or with 1-bromoadamantane in sulfolane affords N-adamantyl derivatives. The adamantylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a59c4fc902c9248def17bf6c9719c4ed
https://doi.org/10.1002/chin.200242178
https://doi.org/10.1002/chin.200242178
Autor:
Pavel A. Slepukhin, Oleg A. Dyachenko, Vladimir L. Rusinov, Eugeny N. Ulomsky, T. S. Shestakova, Oleg N. Chupakhin, S. L. Deev, M. I. Kodess, A. N. Chekhlov, Olga N. Kazheva
Publikováno v:
ChemInform. 38
A new procedure was developed for the synthesis of 6-phenyltetrazolo[1,5-b]triazin-7-one. Aza analogs of uracil and isocytosine were prepared by the tetrazole ring cleavage. It was demonstrated that these transformations can be used in the synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9be083015dbdce938f285664e733ccf9
https://doi.org/10.1002/chin.200736199
https://doi.org/10.1002/chin.200736199
Publikováno v:
ChemInform. 34
The replacement of the amino group with the hydroxy group was examined in the series of 6-aryl- and 6-benzoimidazolyl-7-aminoazolo[5,1-c]-1,2,4-triazines. These reactions provide a convenient synthetic procedure for the preparation of fused azolo[5,1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d57868fe1a6d7548a9bfbcc6427674e
https://doi.org/10.1002/chin.200315170
https://doi.org/10.1002/chin.200315170