Chemical Transformations of 2-(3-Aryl-4-nitrobutanoyl)-5,5-dimethylcyclohexane-1,3-diones: II. Synthesis of New 6,7-Dihydro-1,2-benzoxazol-4(5H)-ones with Functionalized Side Chain
- Authors: Pashkovskii F.S.1, Dontsu Y.S.1, Rubinov D.B.1, Lakhvich F.A.1
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Affiliations:
- Institute of Bioorganic Chemistry
- Issue: Vol 54, No 6 (2018)
- Pages: 844-854
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/218043
- DOI: https://doi.org/10.1134/S1070428018060040
- ID: 218043
Cite item
Abstract
Transformation of the nitromethyl group in 3-(2-aryl-3-nitropropyl)-6,6-dimethyl-6,7-dihydro-1,2-benzoxazol-4(5H)-ones by the Nef reaction gave the corresponding aldehydes. Jones oxidation of the latter afforded carboxylic acids together with oxidative decarboxylation products. The possibility for the construction of heterocyclic fragment on the basis of the formyl or carboxylmethyl group of the resulting 6,7-dihydro-1,2-benzoxazol-4(5H)-one derivatives was studied.
About the authors
F. S. Pashkovskii
Institute of Bioorganic Chemistry
Author for correspondence.
Email: pashkovsky61@mail.ru
Belarus, ul. Akademika Kuprevicha 5/2, Minsk, 220141
Yu. S. Dontsu
Institute of Bioorganic Chemistry
Email: pashkovsky61@mail.ru
Belarus, ul. Akademika Kuprevicha 5/2, Minsk, 220141
D. B. Rubinov
Institute of Bioorganic Chemistry
Email: pashkovsky61@mail.ru
Belarus, ul. Akademika Kuprevicha 5/2, Minsk, 220141
F. A. Lakhvich
Institute of Bioorganic Chemistry
Email: pashkovsky61@mail.ru
Belarus, ul. Akademika Kuprevicha 5/2, Minsk, 220141
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