Zobrazeno 1 - 10
of 64
pro vyhledávání: '"F. A. Akbutina"'
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. 39:75-81
Starting from (+)-Δ3-carene, synthetic equivalents of the C10-C16 fragment of epothilone carbo- analogs were obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4711e930d5f341b79141e20e72c0e4d
https://doi.org/10.1023/a:1023442612661
https://doi.org/10.1023/a:1023442612661
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. 37:695-699
Some geminal dimethyl-substituted functionalized C4-synthons were prepared on the basis of (±)-pantolactone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fd5dcda71a6c888f6ffd45ca30793cf
https://doi.org/10.1023/a:1012404018676
https://doi.org/10.1023/a:1012404018676
Publikováno v:
Russian Chemical Bulletin. 50:1489-1509
The review surveys chemical conversions of 5-substituted 2,3,5-trichloro-4,4-dimethoxycyclopent-2-en-1-ones and related compounds and the possibilities of their use in the synthesis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9ebe6f9a31711397da568da13318c1c
https://doi.org/10.1023/a:1013038427455
https://doi.org/10.1023/a:1013038427455
Autor:
R. V. Bikbulatov, Leonid V. Spirikhin, Mansur S. Miftakhov, F. A. Akbutina, R. R. Akhmetvallev
Publikováno v:
Russian Journal of Organic Chemistry. 39:834-836
4-C-Allyl-1-S-acetyl-2,4-dideoxy-3-O-mesyl-6-O-methoxymethyl-1-sulfanyl-α,β-D-arabinohexopyranoside treated with (Me3Si)2NNa in benzene at room temperature affords a bicyclic product resulting from intramolecular cyclization, and at treatment with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cce0ace0ac291687fdaf323b7b29b961
https://doi.org/10.1023/b:rujo.0000003161.60198.ec
https://doi.org/10.1023/b:rujo.0000003161.60198.ec
Publikováno v:
Russian Journal of Organic Chemistry. 37:356-358
Condensation of (±)-5-allyl-2,3,5-trichloro-4,4-dimethoxy-2-cyclopentenone with phenylethynylmagnesium bromide in THF gave (±)-5α-allyl-2,3,5β-trichloro-4,4-dimethoxy-1α-phenylethynyl-2-cyclopenten-1β-ol which chemoselectively reacted with ozon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::234a55ca5074fb61a578284eff7189d8
https://doi.org/10.1023/a:1012324306438
https://doi.org/10.1023/a:1012324306438