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Synthesis and 13C NMR spectra of 5-alkyl-1,4-diaza- and 5-alkyl-1-aza-4-oxabicyclo [3.3.0]octan-8-ones

Autor: N. N. Sorokin, V. A. Sedavkina, I. V. Lizak

Publikováno v: Chemistry of Heterocyclic Compounds. 23:1129-1132

A group of previously unreported 5-alkyl-1,4-diaza- and 5-alkyl-1-aza-4-oxabicyclo[3.3.0]octan-8-ones have been synthesized from the ethyl esters of γ-ketocarboxylic acids and ethylenediamine or ethanolamine.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cc2cb5c8a103bfbc5e2b2564f08e87d2
https://doi.org/10.1007/bf00476546

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Chemical reactions of 5-alkyl-1,4-diaza- and 5-alkyl-1-aza-4-oxabicyclo[3.3.0]octan-8-ones

Autor: I. V. Lizak, V. A. Sedavkina, N. N. Sorokin

Publikováno v: Chemistry of Heterocyclic Compounds. 24:159-162

The behavior of 5-alkyl-1,4-diaza and 5-alkyl-1-aza-4-oxabicyclo[3.3.0]octan-8-ones has been studied towards catalytic reduction, reduction by lithium aluminum hydride, acylation, cyanoethylation, alkylation, etc. The oxazolidine ring in 5-alkyl-1-az

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e67ec69b9fffecc02b70694cd33d94f9
https://doi.org/10.1007/bf00473324

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