Zobrazeno 1 - 10
of 21
pro vyhledávání: '"S. Kh. Sharipova"'
Autor:
M. L. Tkachenko, L. E. Zhnyakina, A. N. Seryakova, A. V. Lyamin, S. Kh. Sharipova, M. A. Loseva, Yu. V. Moshchensky
Publikováno v:
Pharmaceutical Chemistry Journal. 55:1250-1253
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0e19cb403548ab40f98a386d1021ace
https://doi.org/10.1007/s11094-022-02566-6
https://doi.org/10.1007/s11094-022-02566-6
Autor:
S. Kh. Sharipova, K. N. Sazanova, O. E. Pravdivtseva, N R Varina, E. V. Avdeeva, E. N. Zaitseva, E. P. Gladunova, V. A. Kurkin
Publikováno v:
Pharmaceutical Chemistry Journal. 54:797-799
The flavonoids quercetin and spireoside (quercetin 4′-O-β-D-glucopyranoside) were isolated for the first time from fruit of meadowsweet [Filipendula ulmaria (L.) Maxim.] and identified using UV spectrophotometry, NMR spectroscopy, mass spectrometr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3b53701306ec35b348fcdb8edea366d
https://doi.org/10.1007/s11094-020-02276-x
https://doi.org/10.1007/s11094-020-02276-x
Autor:
Yu. V. Zaitseva, Pascal Coudert, V. P. Zaitsev, S. Kh. Sharipova, M. Madesclaire, A. V. Lyamin
Publikováno v:
Pharmaceutical Chemistry Journal. 49:10-12
A series of new urea derivatives were synthesized from (1S,2S)-2-amino-1-(4-nitrophenyl)-1,3-propanediol and their antimicrobial activities were studied. Of the eight ureas synthesized here, only one compound had weak antimicrobial activity in relati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b9f8517e85c85004fd2bbd30be72fbc
https://doi.org/10.1007/s11094-015-1213-0
https://doi.org/10.1007/s11094-015-1213-0
Publikováno v:
Chemistry of Heterocyclic Compounds. 43:1325-1332
A synthesis is reported for (4R,5R)-and (4S,5S)-4-hydroxymethyl-5-(4-nitrophenyl)oxazolidin-2-ones and (1′R,4R)-and (1′S,4S)-4-[hydroxy(4-nitrophenyl)methyl]oxazolidin-2-ones from (1R,2R)-and (1S,2S)-2-amino-1-(4-nitrophenyl)-1,3-propanediols. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b724ae11bb6164972f42e8f1911a19b6
https://doi.org/10.1007/s10593-007-0201-z
https://doi.org/10.1007/s10593-007-0201-z
Autor:
A. V. Lyamin, S. Kh. Sharipova, V. P. Zaitsev, A. A. Osipova, Yu. V. Zaitseva, E. A. Botkin, M. Madesclaire
Publikováno v:
Pharmaceutical Chemistry Journal. 45:668-670
A series of urea derivatives were synthesized from (1S,2S)-2-amino-1-(4-nitrophenyl)-1,3-propanediol and their antimicrobial activity was studied. The compounds synthesized here showed the greatest levels of activity against strains of Bacillus cereu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21ba2451dc434a2b02cd3fad38974204
https://doi.org/10.1007/s11094-012-0700-9
https://doi.org/10.1007/s11094-012-0700-9
Publikováno v:
Chemistry of Heterocyclic Compounds. 37:898-902
The reaction of (1S,2S)-2-amino-1-(4-nitrophenyl)-1,3-propanediol with glutaraldehyde has been studied. It has been established on the basis of AM1 and PM3 calculations and 1H NMR spectra recorded in the presence of the shift reagent Eu(fod)3 that (1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1340cdf8a393778a5a3ce87b1ac5197
https://doi.org/10.1023/a:1012463911175
https://doi.org/10.1023/a:1012463911175
Publikováno v:
Chemistry of Heterocyclic Compounds. 35:474-478
The reaction of paraformaldehyde with (1S,2S)-2-aryl(hetaryl)methylamino-1-(4-nitrophenyl)-1,3-propanediols produces a mixture of isomeric 3-aryl(hetaryl)methyl-4-hydroxymethyl-5-(4-nitrophenyl)- and 3-aryl(hetary)methyl-4-hydroxy(4-nitrophenyl)methy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0189d6a144da054e5bc548f0c8637e71
https://doi.org/10.1007/bf02319337
https://doi.org/10.1007/bf02319337
Publikováno v:
Pharmaceutical Chemistry Journal. 32:157-160
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41dac22373dcab93a6c771431ba9a274
https://doi.org/10.1007/bf02464198
https://doi.org/10.1007/bf02464198
Publikováno v:
Chemistry of Heterocyclic Compounds. 38:71-73
We have studied hydrazinolysis of (4S,5S)-3-benzyl-4-hydroxymethyl-5-(4-nitrophenyl)oxazolidine, (1R,4S,5S)-1-(4-nitrophenyl)-1-aza-3,7-dioxabicyclo[3,3,0]octane, and (1R,4S,5S)-1-benzyl-4-(4-nitrophenyl)-1-azonia-3,7-dioxabicyclo[3,3,0]octane. We ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89a7d65c8bbceed91b78d3e3cddc3da3
https://doi.org/10.1023/a:1014807426609
https://doi.org/10.1023/a:1014807426609
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37699a6b15bdd1a5e186193bc1af524b
https://doi.org/10.1002/chin.199131138
https://doi.org/10.1002/chin.199131138