Alkylation of CH acids with haloidalkyl-1,3-dioxolanes
- Autores: Raskil’dina G.1, Borisova Y.1, Spirikhin L.1, Zlotsky S.1
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Afiliações:
- Ufa State Petroleum Technological University
- Edição: Volume 87, Nº 5 (2017)
- Páginas: 1097-1100
- Seção: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/220098
- DOI: https://doi.org/10.1134/S1070363217050358
- ID: 220098
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Resumo
Alkylation of diethyl malonate and Meldrum acid with haloalkyl-1,3-dioxolanes has afforded the substituted malonates; their decarboxylation has led to the formation of esters containing a cycloacetal fragment. Reactions of the substituted malonates with urea have yielded the corresponding substituted barbiturates. Monodecarboxylation of the obtained malonates has led to the formation of 1,3-dioxolane-carboxylates.
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Sobre autores
G. Raskil’dina
Ufa State Petroleum Technological University
Autor responsável pela correspondência
Email: graskildina444@mail.ru
Rússia, ul. Kosmonavtov 1, Ufa, 450062
Yu. Borisova
Ufa State Petroleum Technological University
Email: graskildina444@mail.ru
Rússia, ul. Kosmonavtov 1, Ufa, 450062
L. Spirikhin
Ufa State Petroleum Technological University
Email: graskildina444@mail.ru
Rússia, ul. Kosmonavtov 1, Ufa, 450062
S. Zlotsky
Ufa State Petroleum Technological University
Email: graskildina444@mail.ru
Rússia, ul. Kosmonavtov 1, Ufa, 450062