Zobrazeno 1 - 10
of 14
pro vyhledávání: '"E. S. Izmest'ev"'
Publikováno v:
Russian Journal of Organic Chemistry. 59:67-77
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f6ba2958ff86226552626617194cf56
https://doi.org/10.1134/s1070428023010074
https://doi.org/10.1134/s1070428023010074
Publikováno v:
Russian Journal of Organic Chemistry. 58:1170-1177
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a804d292fb3b57721146f73e67267e8
https://doi.org/10.1134/s1070428022080139
https://doi.org/10.1134/s1070428022080139
Publikováno v:
Russian Journal of Organic Chemistry. 56:1392-1398
A series of asymmetric disulfides was obtained in yields of 38–50% by the co-oxidation of a mixture of diterpene abietane-derived thiols and thiols synthesized from protected monosaccharides with galacto-, fructo-, and glucopyranose and ribofuranos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb2dc67f16c3229db6af1fe6d4b483b6
https://doi.org/10.1134/s1070428020080096
https://doi.org/10.1134/s1070428020080096
Autor:
Galina B. Guseva, S.V. Efimov, Elena V. Antina, Vladimir V. Klochkov, Alexander A. Ksenofontov, Liliya E. Nikitina, Airat R. Kayumov, Zulfiya R. Azizova, E. S. Izmest’ev, S. V. Pestova, Svetlana A. Rubtsova, Pavel S. Bocharov, Mikhail B. Berezin, Roman S. Pavelyev, S V Kiselev, Ilmir R. Gilfanov, Anastassia S. Smirnova, Olga V. Ostolopovskaya, Ilya A. Khodov
Publikováno v:
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 268
This paper is devoted to the design of a fluorescent probe based on meso-carboxysubstituted-BODIPY with a thioterpene fragment. The functional replacement of the methoxy group in the BODIPY molecule on a thioterpene fragment was carried out in order
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c47cb6dffb7c89bbf6d7ea045cd942b
https://pubmed.ncbi.nlm.nih.gov/34840052
https://pubmed.ncbi.nlm.nih.gov/34840052
Autor:
Larisa L. Frolova, O. N. Grebyonkina, A. V. Kutchin, O. M. Lezina, E. S. Izmest’ev, Svetlana A. Rubtsova
Publikováno v:
Russian Journal of Organic Chemistry. 55:1469-1475
cis-Myrtanethiol and a mixture of diastereoisomeric myrtanethiols were synthesized starting from (-)-β-pinene. Their oxidation with chlorine dioxide afforded a number of derivatives such as disulfides, S-thiol-sulfonates, sulfonyl chlorides, and sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5276b5c3aad5faf27209aced21d78ca
https://doi.org/10.1134/s107042801910004x
https://doi.org/10.1134/s107042801910004x
Publikováno v:
Russian Journal of Organic Chemistry. 54:1395-1401
Optically active derivatives of 3,4-dihydropyrimidin-2(1H)-one have been synthesized on the basis of myrtenal and methyl 2,3-O-isopropylidene-α-L-erythro-pentodialdo-1,4-furanoside in 45 and 50% yields, respectively, and subjected to stereoselective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99bf2dbec790254f1a3985384bf3efe3
https://doi.org/10.1134/s107042801809021x
https://doi.org/10.1134/s107042801809021x
Publikováno v:
Russian Journal of Organic Chemistry. 54:1041-1044
A number of thioglycosides derived from benzoylated glucopyranose and nitrogen-containing heterocyclic thiols have been synthesized in up to 98% yield, and benzoyl protecting groups have been removed from the glycoside with a 3-phenyl-4-oxo-3,4-dihyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fad52001d8a9461cb71a9d1f19193a40
https://doi.org/10.1134/s1070428018070126
https://doi.org/10.1134/s1070428018070126
Autor:
Patrick Rollin, Alina F. Saifina, I. Z. Rakhmatullin, Olga V. Ostolopovskaya, S. V. Pestova, Roman S. Pavelyev, Vladimir V. Klochkov, D. P. Gerasimova, Svetlana A. Rubtsova, Daut R. Islamov, Dmitry V. Zakharychev, Olga A. Lodochnikova, E. S. Izmest’ev, Liliya E. Nikitina
Publikováno v:
Journal of Molecular Structure. 1239:130491
The physico-chemical characteristics and crystal structure of newly synthesized isobornanyl sulfoxides and sulfone are presented. After purification, diastereomeric sulfoxides were obtained in a 2:1 eutectic ratio, which did not allow either separati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3234f2cbface992fd5cd023090580fe0
https://doi.org/10.1016/j.molstruc.2021.130491
https://doi.org/10.1016/j.molstruc.2021.130491
Autor:
E. S. Izmest’ev, O. N. Grebyonkina, A. V. Kutchin, D. V. Sudarikov, S. V. Pestova, O. M. Lezina, Svetlana A. Rubtsova
Publikováno v:
Russian Journal of Organic Chemistry. 53:860-868
The oxidation of monoterpene thiols with chlorine dioxide afforded new water-soluble sulfonic acids and their derivatives (sulfonothioates and sulfonyl chlorides). The reaction of terpene thiols with ClO2 gave the corresponding trisulfides. Sulfonoth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd313d9e4f72cf79afb5a96cdf45f216
https://doi.org/10.1134/s1070428017060082
https://doi.org/10.1134/s1070428017060082
Publikováno v:
Russian Journal of Bioorganic Chemistry. 43:302-310
Hydroxyl- and chloroethyl derivatives of neomenthane- and isobornanethiol in yields of to 80% were synthesized. They served as the basis for the preparation of new bis-sulfides with diacetone-protected galacto- and fructopyranose fragments in yields
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12af22d5229fc1c827b9effca7c6984e
https://doi.org/10.1134/s1068162017030141
https://doi.org/10.1134/s1068162017030141