Synthesis of 3,4-diaryl-5-carboxy-4,5-dihydroisoxazole 2-oxides as valuable synthons for anticancer molecules

The convenient regioselective scalable synthesis of 3,4-diaryl-5-carboxy-4,5-dihydroisoxazole 2-oxides was developed based on a condensation of simple starting materials (arylbenzaldehydes, arylnitromethanes, and ethoxycarbonylmethylpyridinium bromide) under mild conditions. The obtained synthons can be applied for the synthesis of 3,4-diarylisoxazole derivatives capable of suppressing malignant growth. © 2017 Elsevier Ltd

Authors
Chernysheva N.B.1 , Maksimenko A.S.1 , Andreyanov F.A.1 , Kislyi V.P.1 , Strelenko Y.A.1 , Khrustalev V.N. 2, 3 , Semenova M.N.4 , Semenov V.V.1
Journal
Number of issue
48
Language
English
Pages
6728-6735
Status
Published
Volume
73
Year
2017
Organizations
  • 1 N. D. Zelinsky Institute of Organic Chemistry, RAS, 47 Leninsky Prospect, Moscow, 119991, Russian Federation
  • 2 Faculty of Science, RUDN University, 6 Miklukho-Maklay Street, Moscow, 117198, Russian Federation
  • 3 A. N. Nesmeyanov Institute of Organoelement Compounds, RAS, 28 Vavilov Street, Moscow, 119991, Russian Federation
  • 4 N. K. Koltzov Institute of Developmental Biology, RAS, 26 Vavilov Street, Moscow, 119334, Russian Federation
Keywords
3,4-Diarylisoxazoles; 3,4-Diarylisoxazoline oxides; Anticancer synthons; Carbonylmethylpyridinium
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/5173/
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