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Title: Convenient synthesis of substituted 5-(hydroxymethyl)-8-methyl-3(4-phenylquinazolin-2-yl)-2H-pyrano [2,3-c]pyridin-2-ones
Authors: Zhuravel, I. O.
Kovalenko, S. M.
Ivachtchenko, A. V.
Chernykh, V. P.
Shinkarenko, P. E.
Журавель, І. О.
Коваленко, С. М.
Іващенко, А. В.
Черних, В. П.
Шинкаренко, П. Є.
Журавель, И. А.
Коваленко, С. Н.
Иващенко, А. В.
Черных, В. П.
Шинкаренко, П. Е.
Keywords: 2H-Pyrano[2,3-c]pyridin-2-one;quinazoline;recyclization
Issue Date: 2005
Bibliographic description (Ukraine): Convenient synthesis of substituted 5-(hydroxymethyl)-8-methyl-3(4-phenylquinazolin-2-yl)-2H-pyrano [2,3-c]pyridin-2-ones / I. O. Zhuravel, S. M. Kovalenko, A. V. Ivachtchenko, V. P. Chernykh, P. E. Shinkarenko // Synthetic communications. - 2005. - № 35. - Р. 1641-1647.
Abstract: Interaction of 2-imino-2H-pyrano[2,3-c]pyridin-3-carboxamide with substituted 2-aminobenzophenones proceeds via recyclization mechanism leading to substituted 3-(4-arylquinazolyn-2-yl)-2H-pyrano[2,3-c]pyridin-2-ones. Their reaction with acetic anhydride affords the O-acylation products.
Appears in Collections:Наукові публікації В. П. Черних

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