Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mikhail A. Khohodorkovskiy"'
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:
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