Аннотация:O-Vinyl acetoxime reacts with trifluoroacetic anhydride (pyridine, room temperature) to form (E)-O-[2-(trifluoroacetyl)vinyl] acetoxime or 5-hydroxy-5-trifluoromethyl-4,5-dihydro-1,2-oxazole.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
B. A. Trofimov, E. Yu. Schmidt, A. I. Mikhaleva, A. M. Vasil'tsov, L. I. Larina, L. V. Klyba, “Trifluoroacetylation of O-vinyl acetoxime”, Mendeleev Commun., 9:6 (1999), 238–239
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4615
https://www.mathnet.ru/rus/mendc/v9/i6/p238
Эта публикация цитируется в следующих 7 статьяx:
R.B. Lincoln, Catalysis from A to Z, 2020
E. Yu. Schmidt, I. A. Ushakov, N. V. Zorina, A. I. Mikhaleva, B. A. Trofimov, “The reaction of 2-arylazo-1-vinylpyrroles with trifluoroacetic anhydride: unexpected formation of N-aryl-2,2,2-trifluoroacetamides and conjugated polymers”, Mendeleev Commun., 21:1 (2011), 36–37
Edgars Abele, Edmunds Lukevics, Patai's Chemistry of Functional Groups, 2010
Sergey V. Druzhinin, Elizabeth S. Balenkova, Valentine G. Nenajdenko, “Recent advances in the chemistry of α,β-unsaturated trifluoromethylketones”, Tetrahedron, 63:33 (2007), 7753
Alexey B Zaitsev, Alexander M Vasil'tsov, Elena Yu Schmidt, Al'bina I Mikhaleva, Ludmila V Morozova, Andrey V Afonin, Igor' A Ushakov, Boris A Trofimov, “O-Vinyldiaryl- and O-vinylaryl(hetaryl)ketoximes: a breakthrough in O-vinyloxime chemistry”, Tetrahedron, 58:50 (2002), 10043
Edmunds Lukevics, Edgars Abele, “Recent Advances in the Synthesis of Heterocycles from Oximes”, HETEROCYCLES, 53:10 (2000), 2285
Boris A. Trofimov, Elena Yu. Schmidt, Al'bina I. Mikhaleva, Alexander M. Vasil'tsov, Ludmila I. Larina, Ludmila V. Klyba, “ChemInform Abstract: Trifluoroacetylation of O‐Vinyl Acetoxime.”, ChemInform, 31:21 (2000)
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