Zobrazeno 1 - 10
of 76
pro vyhledávání: '"R. R. Akhmetvaleev"'
Autor:
A F Khamitova, N Sh Zagidullin, Sh Z Zagidullin, R R Akhmetvaleev, I A Lakman, D.F. Gareeva, E L Tulbaev
Publikováno v:
Kardiologiia. 60(3)
Objective To study the prognostic role of current serum biomarkers in patients with myocardial infarction (MI) by constructing a multifactorial model for prediction of cardiovascular complications (CVC) in remote MI. Acute coronary syndrome is a majo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20640c612fbe5816803acee06284d38b
https://pubmed.ncbi.nlm.nih.gov/32375611
https://pubmed.ncbi.nlm.nih.gov/32375611
Autor:
R. R. Akhmetvaleev, Mansur S. Miftakhov, T. A. Belogaeva, F. A. Akbutina, G. A. Shavaleeva, A. M. Karimova
Publikováno v:
Russian Journal of Organic Chemistry. 39:1719-1723
Starting from 2,3-dichloro-4,4-ethylenedioxy-2-cyclopentenone, a practical procedure has been developed for the synthesis of a series of 4-substituted 2-chloro-4-hydroxycyclopentenones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::405391bf0e79a051d5e8eca5ff9f6489
https://doi.org/10.1023/b:rujo.0000019734.67980.35
https://doi.org/10.1023/b:rujo.0000019734.67980.35
Publikováno v:
Russian Journal of Organic Chemistry. 39:1489-1492
The reduction of 2-chloro-4,4-ethylenedioxy-3-phenylsulfanyl-2-cyclopentenone with sodium tetra-hydridoborate in ethanol yields 3-chloro-4-hydroxy-2-phenylsulfanyl-2-cyclopentenone, while with the use of lithium aluminum hydride in tetrahydrofuran or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::879b77ebf7f65450d5bf9bb0b19baf26
https://doi.org/10.1023/b:rujo.0000010567.22691.a5
https://doi.org/10.1023/b:rujo.0000010567.22691.a5
Publikováno v:
Russian Journal of Organic Chemistry. 39:1493-1496
2,3-Dichloro- and 2,3,5-trichloro-4,4-ethylenedioxy-2-cyclopentenones react with allyl and benzyl alcoholates and thiolates and benzylamine to give products resulting from AdNE substitution of the 3-chlorine atom, [1,3]-sigmatropic rearrangement, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::936003bbe10e75bcbf0f37c17555ed0a
https://doi.org/10.1023/b:rujo.0000010568.07788.3d
https://doi.org/10.1023/b:rujo.0000010568.07788.3d
Publikováno v:
Russian Journal of Organic Chemistry. 39:658-662
Starting from levoglucosan, 1,6-anhydro-2,4-dideoxy-4-C-(2Z-octenyl)-β-D-arabino-hexopyranose was synthesized and converted into 9-oxo-9-LO thromboxan δ-lactone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d28a9ef4b09f9d1c70fc8c3550b7eaf6
https://doi.org/10.1023/a:1026053111451
https://doi.org/10.1023/a:1026053111451
Publikováno v:
Russian Journal of Organic Chemistry. 38:487-490
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::764ab17a13fca585a4502f313462625d
https://doi.org/10.1023/a:1016582703009
https://doi.org/10.1023/a:1016582703009
Publikováno v:
Russian Journal of Organic Chemistry. 38:361-364
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41245ca9d9453cfb1a1992068b4eba8d
https://doi.org/10.1023/a:1016325923944
https://doi.org/10.1023/a:1016325923944
Publikováno v:
Russian Journal of Organic Chemistry. 38:365-369
Starting from levoglucosan, methyl 2,4-dideoxy-3-O-mesyl-4-C-[(2Z)-octenyl]-α-D-arabino-hexopyranoside and (+)-2α-methoxy-6β-[6-methoxycarbonyl-3-oxo-(1E)-hexenyl]-5α-[(2Z)-octenyl]pyran-3-one were synthesized as potential building blocks for pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dc979513b68f3860938fb9aaa692af8
https://doi.org/10.1023/a:1016377908014
https://doi.org/10.1023/a:1016377908014
Publikováno v:
Russian Journal of Organic Chemistry. 37:1083-1087
Analog of chlorvulone II containing an extra chlorine atom at C11 was synthesized starting with 1,4-dioxa-6,7-dichlorospiro[4.4]non-6-ene.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7cce940bad7a4a1083403915f713446
https://doi.org/10.1023/a:1013171810228
https://doi.org/10.1023/a:1013171810228
Publikováno v:
Russian Journal of Organic Chemistry. 37:1079-1082
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59de67bddbfa6e36b722c31a520f154e
https://doi.org/10.1023/a:1013119826158
https://doi.org/10.1023/a:1013119826158