Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Iosyp O. Opeida"'
Autor:
Dmitry S. Ryabukhin, Dmitry N. Zakusilo, Mikhail O. Kompanets, Anton A.Tarakanov, Irina A. Boyarskaya, Tatiana O. Artamonova, Mikhail A. Khohodorkovskiy, Iosyp O. Opeida, Aleksander V. Vasilyev
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2125-2135 (2016)
The reaction of 5-hydroxymethylfurfural (5-HMF) with arenes in superacidic trifluoromethanesulfonic acid (triflic acid, TfOH) as the solvent at room temperature for 1–24 h gives rise to 5-arylmethylfurfurals (yields of 17–91%) and 2-arylmethyl-5-
Externí odkaz:
https://doaj.org/article/7f606e7e104f46c3a10913ea08f76e82
Autor:
Mykhailo O. Kompanets, O. O. Zosenko, A. N. Shendrik, Yurii E. Litvinov, Iosyp O. Opeida, O. V. Kushch
Publikováno v:
ChemistrySelect. 4:11826-11832
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a265eb86fcea2fc20e62887d337d9c20
https://doi.org/10.1002/slct.201902597
https://doi.org/10.1002/slct.201902597
Autor:
T. O. Artamonova, Aleksander V. Vasilyev, Anton A.Tarakanov, Irina A. Boyarskaya, Mikhail O. Kompanets, Dmitry S. Ryabukhin, Dmitry N. Zakusilo, Iosyp O. Opeida, Mikhail A. Khohodorkovskiy
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2125-2135 (2016)
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2125-2135 (2016)
The reaction of 5-hydroxymethylfurfural (5-HMF) with arenes in superacidic trifluoromethanesulfonic acid (triflic acid, TfOH) as the solvent at room temperature for 1–24 h gives rise to 5-arylmethylfurfurals (yields of 17–91%) and 2-arylmethyl-5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d00caf3fd22e50af9264a54b14c3a982
https://pubmed.ncbi.nlm.nih.gov/27829919
https://pubmed.ncbi.nlm.nih.gov/27829919
Autor:
Iosyp O. Opeida, Wolodymyr Ya. Suprun
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1273-1279
The structure–reactivity relationship in the chain propagation step of radical chain oxidation of styrenes substituted in the ring (ortho, meta and para) and in the vinyl group (position α and β), the addition of a peroxyl radical to the double b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::120e1b9d61d51ff314fb8e605e9d8407
https://doi.org/10.1039/a905404i
https://doi.org/10.1039/a905404i
Autor:
Iosyp O. Opeida, Wolodymyr Ya. Suprun
Publikováno v:
ChemInform. 31
The structure–reactivity relationship in the chain propagation step of radical chain oxidation of styrenes substituted in the ring (ortho, meta and para) and in the vinyl group (position α and β), the addition of a peroxyl radical to the double b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8f21330c8a99055fa10324ddf0573ce
https://doi.org/10.1002/chin.200037018
https://doi.org/10.1002/chin.200037018