Alkylation of 5,5-Substituted N-[4-Methyl-3-phenylfuran-2(5H)-ylidene]-N′-phenylthioureas
- Autores: Avetisyan K.S.1, Galstyan L.K.1
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Afiliações:
- Yerevan State University
- Edição: Volume 55, Nº 7 (2019)
- Páginas: 974-977
- Seção: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/220863
- DOI: https://doi.org/10.1134/S1070428019070091
- ID: 220863
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Resumo
The alkylation of 5,5-disubstituted N-[4-methyl-3-phenylfuran-2(5H)-ylidene]-N′-phenylthioureas with ethyl chloroacetate in the presence of potassium carbonate at a ratio of 1:1:0.6 led to the formation of the corresponding S-(ethoxycarbonylmethyl) derivatives. The reaction with an equimolar amount of potassium carbonate involved intramolecular cyclization of the alkylation products to give spirocyclic compounds.
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Sobre autores
K. Avetisyan
Yerevan State University
Autor responsável pela correspondência
Email: k_avetisyan@ysu.am
Armênia, Yerevan
L. Galstyan
Yerevan State University
Email: k_avetisyan@ysu.am
Armênia, Yerevan
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